Patent Application
20230123277
Sickle cell disease is an inherited condition in which mutated hemoglobin polymerizes in red blood cells. This polymerization causes red blood cells to adopt a sickle or crescent shape which can lead to premature death of red blood cells and thus insufficient numbers of healthy red blood cells, in turn causing pain, increased susceptibility to infection, fatigue, and blockage of blood vessels. Individuals with sickle cell disease are at increased risk of stroke and clotting disorders, blindness, gallstones, pulmonary hypertension, pregnancy complications, and organ damage and many of those affected die prematurely.
Thalassemia is another inherited blood disorder in which abnormal hemoglobin or an inadequate amount of hemoglobin is produced. Various forms of thalassemia are possible depending on where the mutation in hemoglobin is found (e.g., α-globin or β-globin chain proteins) and whether a person has one or two defective genes; these forms vary in the severity of symptoms. Children born with thalassemia can appear normal at birth but may later develop anemia, bone deformities, fatigue, shortness of breath, stunted growth, and/or jaundice. In some cases, thalassemia can result in stillbirth.
During the development of a fetus, fetal hemoglobin (HbF) is the predominant form of hemoglobin. After birth, adult hemoglobin (HbA) is normally produced, while HbF genes are silenced by DNA methylation enzymes including DNA methyltransferase 1 (DNMT1). Induction of HbF production has typically been effective in the amelioration of clinical symptoms of sickle cell disease and thalassemia.
DNA methylation is also widely studied as an epigenetic modification in mammals and can be implicated in the development of certain cancers. For example, aberrant DNMT activity may result in hypermethylation of tumor-suppressor genes, of DNA that relates to the expression noncoding microRNAs, or in the promoter regions of other genes related to DNA repair. Thus, regulation of DNMT activity can be a useful approach for cancer therapy and/or the treatment of diseases associated with abnormal cell proliferation.
Cytidine analogs, including 5-aza-4′-thio-2′-deoxycytidine and 5-fluoro-2′-deoxycytidine, have been evaluated in cancer clinical trials for anti-DNMT activity. 5-aza-4′-thio-2′-deoxycytidine and 5-fluoro-2′-deoxycytidine have not been evaluated as therapeutic agents for sickle cell disease, thalassemia or anemia disorders. Although these compounds have shown potent in vitro activity and in vivo pharmacokinetic properties, they have shown no significant therapeutic response in pediatric brain tumor models and have thus been deprioritized for certain cancer treatments. However, treatments with cytidine analogs have traditionally been carried out intravenously, which can lead to lack of patient compliance and exhibit severe genotoxic and cytotoxic effects. Furthermore, IV administration may not result in a sustained exposure to the analogs over a given time-course of treatment and results in limited or negligible distribution of effective therapeutic dose to diseased tissues, like spleen and liver. Furthermore, current dosage forms of cytidine analogs administered concurrently with tetrahydrouridine have exhibited cytotoxic effects.
Despite advances in hematology, there is still a scarcity of compounds and compositions that are potent, efficacious, and selective inhibitors of DNA methyltransferase 1 enzymes and also effective in the treatment of hematological disorders associated with DNMT1 activity and diseases associated with abnormal cell proliferation in which DNMT1 is involved. Additionally, existing treatments may require hardships such as traveling to medical facilities for infusions, which may decrease patient compliance. Ideally, a treatment for a blood disorder such as sickle cell disease or thalassemia could be administered to a subject at home in a single dosage form, would be acid-stable, would be in a low dose with few or no side effects including no cytotoxic effects, and would be capable of timed or sequential release of separate ingredients for maximum synergistic therapeutic effects. These needs and other needs are satisfied by the present disclosure.
In accordance with the purpose(s) of the present disclosure, as embodied and broadly described herein, the disclosure, in one aspect, relates to pharmaceutical compositions comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and methods of using same for treating hematological disorders using the same. In a still further aspect, the disclosure relates to kits comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph useful for treating hematological disorders.
In various aspects, the disclosed methods comprise a method for treating a hematological disorder in a subject, the method comprising administering a therapeutic agent; wherein first therapeutic agent is 5-aza-4′-thio-2′-deoxycytidine having a structure represented by the formula:
and, wherein the therapeutic agent is a crystalline polymorph selected from polymorph Form A and polymorph Form F; wherein polymorph Form A has a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ; and wherein polymorph Form F has a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ.
Other systems, methods, features, and advantages of the present disclosure will be or become apparent to one with skill in the art upon examination of the following drawings and detailed description. It is intended that all such additional systems, methods, features, and advantages be included within this description, be within the scope of the present disclosure, and be protected by the accompanying claims. In addition, all optional and preferred features and modifications of the described embodiments are usable in all aspects of the disclosure taught herein. Furthermore, the individual features of the dependent claims, as well as all optional and preferred features and modifications of the described embodiments are combinable and interchangeable with one another.
The drawings described herein are for illustrative purposes only of selected embodiments and not all possible implementations, and are not intended to limit the scope of the present disclosure.
Additional advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or can be learned by practice of the invention. The advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
Many modifications and other embodiments disclosed herein will come to mind to one skilled in the art to which the disclosed compositions and methods pertain having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the disclosures are not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims. The skilled artisan will recognize many variants and adaptations of the aspects described herein. These variants and adaptations are intended to be included in the teachings of this disclosure and to be encompassed by the claims herein.
Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.
As will be apparent to those of skill in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several embodiments without departing from the scope or spirit of the present disclosure.
Any recited method can be carried out in the order of events recited or in any other order that is logically possible. That is, unless otherwise expressly stated, it is in no way intended that any method or aspect set forth herein be construed as requiring that its steps be performed in a specific order. Accordingly, where a method claim does not specifically state in the claims or descriptions that the steps are to be limited to a specific order, it is no way intended that an order be inferred, in any respect. This holds for any possible non-express basis for interpretation, including matters of logic with respect to arrangement of steps or operational flow, plain meaning derived from grammatical organization or punctuation, or the number or type of aspects described in the specification.
All publications and patents cited in this specification are cited to disclose and describe the methods and/or materials in connection with which the publications are cited. All such publications and patents are herein incorporated by references as if each individual publication or patent were specifically and individually indicated to be incorporated by reference. Such incorporation by reference is expressly limited to the methods and/or materials described in the cited publications and patents and does not extend to any lexicographical definitions from the cited publications and patents. Any lexicographical definition in the publications and patents cited that is not also expressly repeated in the instant application should not be treated as such and should not be read as defining any terms appearing in the accompanying claims. The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present disclosure is not entitled to antedate such publication by virtue of prior disclosure. Further, the dates of publication provided could be different from the actual publication dates that may need to be independently confirmed.
While aspects of the present disclosure can be described and claimed in a particular statutory class, such as the system statutory class, this is for convenience only and one of skill in the art will understand that each aspect of the present disclosure can be described and claimed in any statutory class.
It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only and is not intended to be limiting. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the disclosed compositions and methods belong. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly defined herein.
Aspects of the present disclosure will employ, unless otherwise indicated, techniques of molecular biology, microbiology, organic chemistry, biochemistry, physiology, cell biology, blood vessel biology, and the like, which are within the skill of the art. Such techniques are explained fully in the literature.
Prior to describing the various aspects of the present disclosure, the following definitions are provided and should be used unless otherwise indicated. Additional terms may be defined elsewhere in the present disclosure.
As used herein, “comprising” is to be interpreted as specifying the presence of the stated features, integers, steps, or components as referred to, but does not preclude the presence or addition of one or more features, integers, steps, or components, or groups thereof. Moreover, each of the terms “by”, “comprising,” “comprises”, “comprised of,” “including,” “includes,” “included,” “involving,” “involves,” “involved,” and “such as” are used in their open, non-limiting sense and may be used interchangeably. Further, the term “comprising” is intended to include examples and aspects encompassed by the terms “consisting essentially of” and “consisting of.” Similarly, the term “consisting essentially of” is intended to include examples encompassed by the term “consisting of.
As used in the specification and the appended claims, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a filler,” “a 2′-deoxycytidine analog,” or “an excipient,” includes, but is not limited to, combinations of two or more such fillers, 2′-deoxycytidine analogs, or excipients, and the like.
It should be noted that ratios, concentrations, amounts, and other numerical data can be expressed herein in a range format. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. It is also understood that there are a number of values disclosed herein, and that each value is also herein disclosed as “about” that particular value in addition to the value itself. For example, if the value “10” is disclosed, then “about 10” is also disclosed. Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms a further aspect. For example, if the value “about 10” is disclosed, then “10” is also disclosed.
Where a range is expressed, a further aspect includes from the one particular value and/or to the other particular value. Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the disclosure. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges and are also encompassed within the disclosure, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure. For example, where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure, e.g. the phrase “x to y” includes the range from ‘x’ to ‘y’ as well as the range greater than ‘x’ and less than ‘y’. The range can also be expressed as an upper limit, e.g. ‘about x, y, z, or less’ and should be interpreted to include the specific ranges of ‘about x’, ‘about y’, and ‘about z’ as well as the ranges of ‘less than x’, less than y’, and ‘less than z’. Likewise, the phrase ‘about x, y, z, or greater’ should be interpreted to include the specific ranges of ‘about x’, ‘about y’, and ‘about z’ as well as the ranges of ‘greater than x’, greater than y’, and ‘greater than z’. In addition, the phrase “about ‘x’ to ‘y’”, where ‘x’ and ‘y’ are numerical values, includes “about ‘x’ to about ‘y’”.
It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a numerical range of “about 0.1% to 5%” should be interpreted to include not only the explicitly recited values of about 0.1% to about 5%, but also include individual values (e.g., about 1%, about 2%, about 3%, and about 4%) and the sub-ranges (e.g., about 0.5% to about 1.1%; about 5% to about 2.4%; about 0.5% to about 3.2%, and about 0.5% to about 4.4%, and other possible sub-ranges) within the indicated range.
Disclosed are the components to be used to prepare the compositions of the invention as well as the compositions themselves to be used within the methods disclosed herein. These and other materials are disclosed herein, and it is understood that when combinations, subsets, interactions, groups, etc. of these materials are disclosed that while specific reference of each various individual and collective combinations and permutation of these compounds cannot be explicitly disclosed, each is specifically contemplated and described herein. For example, if a particular compound is disclosed and discussed and a number of modifications that can be made to the compound are discussed, specifically contemplated is each and every combination and permutation of the compound and the modifications that are possible unless specifically indicated to the contrary. Thus, if a class of molecules A, B, and C are disclosed as well as a class of molecules D, E, and F and an example of a combination molecule, A-D is disclosed, then even if each is not individually recited each is individually and collectively contemplated meaning combinations, A-E, A-F, B-D, B-E, B-F, C-D, C-E, and C-F are considered disclosed. Likewise, any subset or combination of these is also disclosed. Thus, for example, the sub-group of A-E, B-F, and C-E would be considered disclosed. This concept applies to all aspects of this application including, but not limited to, steps in methods of making and using the compositions of the invention. Thus, if there are a variety of additional steps that can be performed it is understood that each of these additional steps can be performed with any specific embodiment or combination of embodiments of the methods of the invention.
It is understood that the compositions disclosed herein have certain functions. Disclosed herein are certain structural requirements for performing the disclosed functions, and it is understood that there are a variety of structures that can perform the same function that are related to the disclosed structures, and that these structures will typically achieve the same result.
As used herein, the terms “about,” “approximate,” “at or about,” and “substantially” mean that the amount or value in question can be the exact value or a value that provides equivalent results or effects as recited in the claims or taught herein. That is, it is understood that amounts, sizes, formulations, parameters, and other quantities and characteristics are not and need not be exact, but may be approximate and/or larger or smaller, as desired, reflecting tolerances, conversion factors, rounding off, measurement error and the like, and other factors known to those of skill in the art such that equivalent results or effects are obtained. In some circumstances, the value that provides equivalent results or effects cannot be reasonably determined. In such cases, it is generally understood, as used herein, that “about” and “at or about” mean the nominal value indicated ±10% variation unless otherwise indicated or inferred. In general, an amount, size, formulation, parameter or other quantity or characteristic is “about,” “approximate,” or “at or about” whether or not expressly stated to be such. It is understood that where “about,” “approximate,” or “at or about” is used before a quantitative value, the parameter also includes the specific quantitative value itself, unless specifically stated otherwise.
The term “substantially similar to,” as used herein, refers to a powder X-ray diffraction pattern that is non-identical to those depicted herein but shares a majority of major peaks, which fall within the limits of experimental error.
As used herein, the terms “optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where said event or circumstance occurs and instances where it does not.
5-Aza-4′-thio-2′-deoxycytidine (also known as NTX-301) refers to a modified cytidine nucleoside where the ring oxygen on the sugar moiety of the nucleoside is replaced with a sulfur. Aza-T-dCyd has the following structure:
Unless otherwise noted, the term “aza-T-dCyd” includes the compound itself and also pharmaceutically acceptable salts thereof.
Crystalline polymorphs of aza-T-dCyd refer to various crystal structures of the nucleoside. In some embodiments, the crystalline polymorph of aza-T-dCyd refers to Form A, Form B, Form C1, Form C2, Form D1, Form D2, Form E, Form F, Form G1, Form G2, Form H, Form 1, or Form J as further described in the present specification including Examples. In particular embodiments, the crystalline polymorph is Form A or Form F.
The term “polymorph Form A” or “Form A” refers to a crystalline form of aza-T-dCyd that exhibits an X-ray powder diffraction pattern substantially the same as that shown in
The term “polymorph Form F” or “Form F” refers to a crystalline form of aza-T-dCyd that exhibits an X-ray powder diffraction pattern substantially the same as that shown in
As used herein, “DNA methyltransferase 1” and “DNMT1” can be used interchangeably and refer to an enzyme encoded by a gene in humans with a cytogenetic location of 19p13.2 and a molecular location of base pairs 10,133,345-10,194,952 on chromosome 19 (Homo sapiens Annotation Release 109.20190607, GRCh38.p13). The gene structure in humans has at least 37, and possibly as many as 40, exons. DNMT1 has an EC classification of 2.1.1.37, an intracellular location within the nucleus, and catalyzes the transfer of methyl groups to specific CpG structures in DNA. It is the most abundant DNA methyltransferase in mammalian cells and believed to be a key maintenance methyltransferase in mammals. It predominantly methylates hemimethylated CpG di-nucleotides in the mammalian genome via catalyzing the transfer of methyl groups to specific CpG structures in DNA and is responsible for maintaining methylation patterns established in development. The enzyme is about 1620 amino acids long, the first 1100 amino acids constituting the regulatory domain, and the remaining residues constituting the catalytic domain. These are joined by Gly-Lys repeats. Both domains are required for the catalytic function of DNMT1. DNMT1 has also been referred to as CXXC-type zinc finger protein 9, DNA (cytosine-5-)-methyltransferase 1, DNA methyltransferase Hsal, and MCMT.
The term “DNA methyltransferase 1 inhibitor” and “DNMT1 inhibitor” can be used interchangeably and refer to a composition that selectively blocks or inactivates DNMT1. The term “DNA methyltransferase 1 inhibitor” and “DNMT1 inhibitor” also refer to a compound that selectively blocks or inactivates the transfer of methyl groups to specific CpG structures in DNA by the DNMT1. As used herein, the term “selectively blocks or inactivates” refers to a compound that preferentially binds to and blocks or inactivates DNMT1 with a greater affinity and potency, respectively, than its interaction with the other sub-types of the methyltransferase family. Compounds that block or inactivate DNMT1, but that may also block or inactivate other methyltransferase sub-types, as partial or full inhibitors, are contemplated. The term “DNMT1 inhibitor” also refers to a compound that inhibits DNMT1 expression. Typically, a DNMT1 inhibitor compound is a small organic molecule, a polypeptide, an aptamer, an antibody, an intra-antibody, an oligonucleotide or a ribozyme. Tests and assays for determining whether a compound is a DNMT1 inhibitor are well known by the skilled person in the art such as described in Poh et al., Theranostics (2016) 6(3): 369-391. In some instances, the DNMT1 inhibitor can be a 2′-deoxycytidine analog.
As used herein, the term “cytidine deaminase” and “CDA” refers to cytidine deaminase “CDA”, a key enzyme of the pyrimidine salvage pathway that catalyzes the hydrolytic deamination of cytidine and deoxycytidine to uridine and deoxyuridine, respectively 9. Because of the structural similarity to cytidine, several nucleoside-based drugs are also subject to deamination by CDA (Ferraris et al, 2014). In Pancreatic ductal adenocarcinoma, cytidine deaminase “CDA” inactivates gemcitabine via CDA-mediated conversion to difluorodeoxyuridine.
The term “cytidine deaminase inhibitor” or “CDA inhibitor” can be used interchangeably and refer to a composition that selectively blocks or inactivates the cytidine deaminase. The term “cytidine deaminase inhibitor” also refers to a compound that selectively blocks or inactivates hydrolytic deamination mediated by the cytidine deaminase. As used herein, the term “selectively blocks or inactivates” refers to a compound that preferentially binds to and blocks or inactivates CDA with a greater affinity and potency, respectively, than its interaction with the other sub-types of the deaminase family. Compounds that block or inactivate CDA, but that may also block or inactivate other deaminase sub-types, as partial or full inhibitors, are contemplated. The term “CDA inhibitor” also refers to a compound that inhibits CDA expression. Typically, a CDA inhibitor compound is a small organic molecule, a polypeptide, an aptamer, an antibody, an intra-antibody, an oligonucleotide or a ribozyme. Tests and assays for determining whether a compound is a CDA inhibitor are well known by the skilled person in the art such as described in Ferraris et al, 2014; U.S. Pat. No. 6,136,791; WO2009/052287.
As used herein, “administering” can refer to an administration to a subject of one or more therapeutic agents by a route of administration that can be oral, topical, intravenous, subcutaneous, transcutaneous, transdermal, intramuscular, intra-joint, parenteral, intra-arteriole, intradermal, intraventricular, intraosseous, intraocular, intracranial, intraperitoneal, intralesional, intranasal, intracardiac, intraarticular, intracavernous, intrathecal, intravireal, intracerebral, and intracerebroventricular, intratympanic, intracochlear, rectal, vaginal, by inhalation, by catheters, stents or via an implanted reservoir or other device that administers, either actively or passively (e.g. by diffusion) a composition the perivascular space and adventitia. For example a medical device such as a stent can contain a composition or formulation disposed on its surface, which can then dissolve or be otherwise distributed to the surrounding tissue and cells. The term “parenteral” can include subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intralesional, and intracranial injections or infusion techniques. Administration can be continuous or intermittent. In various aspects, a preparation can be administered therapeutically; that is, administered to treat an existing disease or condition. In further various aspects, a preparation can be administered prophylactically; that is, administered for prevention of a disease or condition.
As used interchangeably herein, “subject,” “individual,” or “patient” can refer to a vertebrate organism, such as a mammal (e.g. human). “Subject” can also refer to a cell, a population of cells, a tissue, an organ, or an organism, preferably to human and constituents thereof.
As used herein, the terms “treating” and “treatment” can refer generally to obtaining a desired pharmacological and/or physiological effect. The effect can be, but does not necessarily have to be, prophylactic in terms of preventing or partially preventing a disease, symptom or condition thereof, such as sickle cell disease and/or thalassemia. The effect can be therapeutic in terms of a partial or complete cure of a disease, condition, symptom or adverse effect attributed to the disease, disorder, or condition. The term “treatment” as used herein can include any treatment of sickle cell disease and/or thalassemia in a subject, particularly a human and can include any one or more of the following: (a) preventing the disease from occurring in a subject which may be predisposed to the disease but has not yet been diagnosed as having it; (b) inhibiting the disease, i.e., arresting its development; and (c) relieving the disease, i.e., mitigating or ameliorating the disease and/or its symptoms or conditions. The term “treatment” as used herein can refer to both therapeutic treatment alone, prophylactic treatment alone, or both therapeutic and prophylactic treatment. Those in need of treatment (subjects in need thereof) can include those already with the disorder and/or those in which the disorder is to be prevented. As used herein, the term “treating”, can include inhibiting the disease, disorder or condition, e.g., impeding its progress; and relieving the disease, disorder, or condition, e.g., causing regression of the disease, disorder and/or condition. Treating the disease, disorder, or condition can include ameliorating at least one symptom of the particular disease, disorder, or condition, even if the underlying pathophysiology is not affected, e.g., such as treating the pain of a subject by administration of an analgesic agent even though such agent does not treat the cause of the pain. In one aspect, treatment of sickle cell disease or thalassemia can increase total hemoglobin or increase fetal hemoglobin or reduce anemia or reduce clumping among misshapen erythrocytes.
As used herein, the term “prevent” or “preventing” refers to precluding, averting, obviating, forestalling, stopping, or hindering something from happening, especially by advance action. It is understood that where reduce, inhibit or prevent are used herein, unless specifically indicated otherwise, the use of the other two words is also expressly disclosed.
As used herein, “therapeutic” can refer to treating, healing, and/or ameliorating a disease, disorder, condition, or side effect, or to decreasing in the rate of advancement of a disease, disorder, condition, or side effect.
As used herein, “therapeutic agent” can refer to any substance, compound, molecule, and the like, which can be biologically active or otherwise can induce a pharmacologic, immunogenic, biologic and/or physiologic effect on a subject to which it is administered to by local and/or systemic action. A therapeutic agent can be a primary active agent, or in other words, the component(s) of a composition to which the whole or part of the effect of the composition is attributed. A therapeutic agent can be a secondary therapeutic agent, or in other words, the component(s) of a composition to which an additional part and/or other effect of the composition is attributed. The term therefore encompasses those compounds or chemicals traditionally regarded as drugs, vaccines, and biopharmaceuticals including molecules such as proteins, peptides, hormones, nucleic acids, gene constructs and the like. Examples of therapeutic agents are described in well-known literature references such as the Merck Index (14th edition), the Physicians' Desk Reference (64th edition), and The Pharmacological Basis of Therapeutics (12th edition), and they include, without limitation, medicaments; vitamins; mineral supplements; substances used for the treatment, prevention, diagnosis, cure or mitigation of a disease or illness; substances that affect the structure or function of the body, or pro-drugs, which become biologically active or more active after they have been placed in a physiological environment. For example, the term “therapeutic agent” includes compounds or compositions for use in all of the major therapeutic areas including, but not limited to, adjuvants; anti-infectives such as antibiotics and antiviral agents; analgesics and analgesic combinations, anorexics, anti-inflammatory agents, anti-epileptics, local and general anesthetics, hypnotics, sedatives, antipsychotic agents, neuroleptic agents, antidepressants, anxiolytics, antagonists, neuron blocking agents, anticholinergic and cholinomimetic agents, antimuscarinic and muscarinic agents, antiadrenergics, antiarrhythmics, antihypertensive agents, hormones, and nutrients, antiarthritics, antiasthmatic agents, anticonvulsants, antihistamines, antinauseants, antineoplastics, antipruritics, antipyretics; antispasmodics, cardiovascular preparations (including calcium channel blockers, beta-blockers, beta-agonists and antiarrythmics), antihypertensives, diuretics, vasodilators; central nervous system stimulants; cough and cold preparations; decongestants; diagnostics; hormones; bone growth stimulants and bone resorption inhibitors; immunosuppressives; muscle relaxants; psychostimulants; sedatives; tranquilizers; proteins, peptides, and fragments thereof (whether naturally occurring, chemically synthesized or recombinantly produced); and nucleic acid molecules (polymeric forms of two or more nucleotides, either ribonucleotides (RNA) or deoxyribonucleotides (DNA) including both double- and single-stranded molecules, gene constructs, expression vectors, antisense molecules and the like), small molecules (e.g., doxorubicin) and other biologically active macromolecules such as, for example, proteins and enzymes. The agent may be a biologically active agent used in medical, including veterinary, applications and in agriculture, such as with plants, as well as other areas. The term therapeutic agent also includes without limitation, medicaments; vitamins; mineral supplements; substances used for the treatment, prevention, diagnosis, cure or mitigation of disease or illness; or substances which affect the structure or function of the body; or pro-drugs, which become biologically active or more active after they have been placed in a predetermined physiological environment. As used herein, “therapeutically effective amount” refers to the amount of a disclosed compound or pharmaceutical composition provided herein that is sufficient to effect beneficial or desired biological, emotional, medical, or clinical response of a cell, tissue, system, animal, or human. An effective amount can be administered in one or more administrations, applications, or dosages. The term can also include within its scope amounts effective to enhance or restore to substantially normal physiological function. In general, a “therapeutically effective amount” refers to an amount that is sufficient to achieve the desired therapeutic result or to have an effect on undesired symptoms but is generally insufficient to cause adverse side effects. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration; the route of administration; the rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed and like factors within the knowledge and expertise of the health practitioner and which may be well known in the medical arts. In the case of treating a particular disease or condition, in some instances, the desired response can be inhibiting the progression of the disease or condition. This may involve only slowing the progression of the disease temporarily. However, in other instances, it may be desirable to halt the progression of the disease permanently. This can be monitored by routine diagnostic methods known to one of ordinary skill in the art for any particular disease. The desired response to treatment of the disease or condition also can be delaying the onset or even preventing the onset of the disease or condition.
As used herein, the term “prophylactically effective amount” refers to an amount effective for preventing onset or initiation of a disease or condition.
As used herein, the term “effective amount” can refer to an amount of an inactive ingredient that is sufficient to achieve the desired modification of a physical property of the composition or material. For example, an “effective amount” of a binder refers to an amount that is sufficient to achieve the desired improvement in the property modulated by the formulation component, The specific level in terms of wt % in a composition required as an effective amount will depend upon a variety of factors including the amount and type of binder, amount and type of active ingredient, presence of other components in the formulation, and delivery mechanism of the pharmaceutical composition disclosed herein.
As used herein, a “hematological disorder” refers to a disease or disorder that primarily affects blood and/or blood-forming organs. In some aspects, hematological disorders include genetic disorders such as, for example, sickle cell disease, thalassemia, methemoglobinemia, and the like. In another aspect, hematological disorders can further include anemias, myelodysplastic syndrome, myeloproliferative disorders, coagulopathies, hematological malignancies including, but not limited to, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, and leukemias. In still another aspect, hematological disorders can include hemochromatosis. In any of these aspects, the methods and compositions disclosed herein can be useful for treating hematological disorders.
As used herein, “area-under-the-curve value” describes drug concentration in blood plasma over time. In one aspect, drug concentration is measured at discrete time points and area-under-the-curve is estimated using the trapezoid rule (i.e., a technique for approximating the definite integral of a curve). In one aspect, area-under-the-curve value is useful for approximating bioavailability of a drug over time.
“Maximum plasma concentration” is the peak concentration of a pharmaceutical or drug achieved in the plasma of a subject to whom a drug has been administered. Maximum plasma concentration is typically measured after a first dose but before a second dose is administered.
As used herein, “kit” means a collection of at least two components constituting the kit. Together, the components constitute a functional unit for a given purpose. Individual member components may be physically packaged together or separately. For example, a kit comprising an instruction for using the kit may or may not physically include the instruction with other individual member components. Instead, the instruction can be supplied as a separate member component, either in a paper form or an electronic form which may be supplied on computer readable memory device or downloaded from an internet website, or as recorded presentation.
As used herein, “instruction(s)” means documents describing relevant materials or methodologies pertaining to a kit. These materials may include any combination of the following: background information, list of components and their availability information (purchase information, etc.), brief or detailed protocols for using the kit, trouble-shooting, references, technical support, and any other related documents. Instructions can be supplied with the kit or as a separate member component, either as a paper form or an electronic form which may be supplied on computer readable memory device or downloaded from an internet website, or as recorded presentation. Instructions can comprise one or multiple documents, and are meant to include future updates.
As used herein, “dose” or “dosage” can refer to physically discrete units suitable for use in a subject, each unit containing a predetermined quantity of a disclosed compound and/or a pharmaceutical composition thereof calculated to produce the desired response or responses in association with its administration. The dose can be administered in a single dosage or in multiple dosages, for example from 1 to 4 or more times per day. When multiple dosages are used, the amount of each dosage can be the same or different. Moreover, a dose comprising a first therapeutic agent and a second therapeutic agent can be in separate dosage forms or combined in a single dosage form.
As used herein, “single dosage form”, “single dose”, “unit dosage form”, “unit dose”, and “single dose form” can be used interchangeably and refer to a single drug administration entity combining at least one disclosed therapeutic agent, e.g., a DNMT1 inhibitor such as one or more 2′-deoxycytidine analog, in a therapeutically effective amount, optionally additional disclosed therapeutic agents, a pharmaceutically acceptable carrier, and other excipients, inactive ingredients, and the like as disclosed herein. In various instances, the single dosage form can be a single tablet, capsule, or liquid. That is, “single dosage form” refers to a presentation form comprising a defined amount of at least one disclosed therapeutic agent, with the intention of applying the total of such amount as a single dosage. As an illustration, a representative single dosage of the present disclosure can be a tablet or a capsule comprising at least 2′-deoxycytidine analog in an amount to provide a therapeutically effective dose as disclosed herein below. This aforementioned list of single dosage forms is not intended to be limiting in any way, but merely to represent typical examples of single dosage forms.
It is further understood that a single dosage form refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. That is, a “single dosage form” can be a single dose wherein all active and inactive ingredients are combined in a suitable system, such that the patient or person administering the drug to the patient can open a single container or package with the entire dose contained therein. In some instances, a “single dosage form” can be a powder in a packet or container comprising a therapeutically effective amount of one or more therapeutic agents that can be mixed with a specified volume of liquid. Typical examples of unit dosage forms are tablets (including scored or coated tablets), capsules or pills for oral administration; powder packets; wafers; and segregated multiples thereof. This list of unit dosage forms is not intended to be limiting in any way, but merely to represent typical examples of unit dosage forms.
As used herein, “combined formulation” refers to the mixture of two or more isolated pharmaceutical compositions comprising, e.g., a 2′-deoxycytidine analog and a CDA inhibitor in a representative non-limiting example, into a single dosage form.
As used herein, “combined administration” or “co-administration” refers to administration of two or more isolated pharmaceutical compositions, e.g., a 2′-deoxycytidine analog and a CDA inhibitor in a representative non-limiting example, in separate dosage forms (e.g. separate pills) that can be taken together (simultaneous administration) or in a particular sequence (sequential administration).
As used herein, the terms “mixture” and “combination”, e.g., a combination therapeutic agent, can refer to multiple components or ingredients formed into one resulting component, e.g., a single dosage form comprising components that can be separate but contained in a single dosage form. A combination therapeutic is also inclusive of components that can be administered in the same treatment regimen even if not physically formed into a single component or contained in a single dosage form. As used herein, the terms “mixture” and “combination” may be used interchangeably.
The term “pharmaceutically acceptable” describes a material that is not biologically or otherwise undesirable, i.e., without causing an unacceptable level of undesirable biological effects or interacting in a deleterious manner.
The term “pharmaceutically acceptable carrier” is used herein to refer to a carrier that is useful in preparing a pharmaceutical composition that is generally safe, non-toxic and neither biologically nor otherwise-undesirable, and is acceptable for veterinary use as well as human pharmaceutical use. A “pharmaceutically acceptable carrier” as used in the specification and claims can include both one and more than one such carrier. By “pharmaceutically acceptable” it is meant the carrier must be compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
The term “pharmaceutically acceptable salts”, as used herein, means salts of the active principal agents which are prepared with acids or bases that are tolerated by a biological system or tolerated by a subject or tolerated by a biological system and tolerated by a subject when administered in a therapeutically effective amount. When compounds of the present disclosure contain relatively acidic functionalities, base addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired base, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable base addition salts include, but are not limited to; sodium, potassium, calcium, ammonium, organic amino, magnesium salt, lithium salt, strontium salt or a similar salt. When compounds of the present disclosure contain relatively basic functionalities, acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable acid addition salts include, but are not limited to; those derived from inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the salts derived from relatively nontoxic organic acids like acetic, propionic, isobutyric, maleic, malonic, benzoic, succinic, suberic, fumaric, lactic, mandelic, phthalic, benzenesulfonic, p-tolylsulfonic, citric, tartaric, methanesulfonic, and the like. Also included are salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric acids and the like.
The term “pharmaceutically acceptable ester” refers to esters of compounds of the present disclosure which hydrolyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Examples of pharmaceutically acceptable, non-toxic esters of the present disclosure include C1 to C6 alkyl esters and C5 to C7 cycloalkyl esters, although C1 to C4 alkyl esters are preferred. Esters of disclosed compounds can be prepared according to conventional methods. Pharmaceutically acceptable esters can be appended onto hydroxy groups by reaction of the compound that contains the hydroxy group with acid and an alkylcarboxylic acid such as acetic acid, or with acid and an arylcarboxylic acid such as benzoic acid. In the case of compounds containing carboxylic acid groups, the pharmaceutically acceptable esters are prepared from compounds containing the carboxylic acid groups by reaction of the compound with base such as triethylamine and an alkyl halide, for example with methyl iodide, benzyl iodide, cyclopentyl iodide or alkyl triflate. They also can be prepared by reaction of the compound with an acid such as hydrochloric acid and an alcohol such as ethanol or methanol.
The term “pharmaceutically acceptable amide” refers to non-toxic amides of the present disclosure derived from ammonia, primary C1 to C6 alkyl amines and secondary C1 to C6 dialkyl amines. In the case of secondary amines, the amine can also be in the form of a 5- or 6-membered heterocycle containing one nitrogen atom. Amides derived from ammonia, C1 to C3 alkyl primary amides and C1 to C2 dialkyl secondary amides are preferred. Amides of disclosed compounds can be prepared according to conventional methods. Pharmaceutically acceptable amides can be prepared from compounds containing primary or secondary amine groups by reaction of the compound that contains the amino group with an alkyl anhydride, aryl anhydride, acyl halide, or aroyl halide. In the case of compounds containing carboxylic acid groups, the pharmaceutically acceptable amides are prepared from compounds containing the carboxylic acid groups by reaction of the compound with base such as triethylamine, a dehydrating agent such as dicyclohexyl carbodiimide or carbonyl diimidazole, and an alkyl amine, dialkylamine, for example with methylamine, diethylamine, and piperidine. They also can be prepared by reaction of the compound with an acid such as sulfuric acid and an alkylcarboxylic acid such as acetic acid, or with acid and an arylcarboxylic acid such as benzoic acid under dehydrating conditions such as with molecular sieves added. The composition can contain a compound of the present disclosure in the form of a pharmaceutically acceptable prodrug.
As used herein, “oral administration” or “orally” refers to the introduction of a pharmaceutical composition into a subject by way of the oral cavity (e.g., in liquid or solid form), e.g., a capsule or tablet, although other oral dosage forms are contemplated and disclosed herein. Oral administration is inclusive of dosage forms that are swallowed or ingested by the oral cavity, and transit, in some form, the gastro-intestinal tract such that therapeutic agents are absorbed, at least in part, from the gastro-intestinal tract. It is understood that oral administration is also inclusive of any mode of administration that is by way of the oral cavity, including, but not limited to, sublingual administration and buccal administration.
As used herein, “sublingual administration” or “sublingually” refers to the introduction of a pharmaceutical composition into a subject by application to the mucosal surface under the tongue (within the oral cavity) such that the composition is absorbed into the subject.
As used herein, “buccal administration” or “buccal” refers to the introduction of a pharmaceutical composition into a subject by application to the mucosal surface lining the cheek (within the oral cavity) such that the composition is disintegrated, dissolved and absorbed into the subject. In some instances, disintegration and dissolution occurs in the buccal cavity, followed by absorption of all or a portion of the pharmaceutically active ingredient through the buccal mucosa. The remaining pharmaceutically active ingredient, if any, is then swallowed and absorbed enterally. As used herein, “intranasal administration” or “intranasally” refers to the introduction of a pharmaceutical composition within the nasal cavity.
The disclosed pharmaceutical compositions utilize disclosed therapeutic agents, alone and in various combinations as contemplated herein.
In one aspect, the pharmaceutical compositions disclosed herein comprise a therapeutic agent comprising 5-aza-4′-thio-2′-deoxycytidine, or a pharmaceutically acceptable salt thereof. It is understood that 5-aza-4′-thio-2′-deoxycytidine is a compound having a structure represented by the formula:
In a further aspect, the Aza-T-dCyd used a crystalline polymorph as described herein below.
In a further aspect, a therapeutic agent, such as 5-aza-4′-thio-2′-deoxycytidine can optionally be utilized in combination with one or more tetrahydrouridine compound or derivative. In a still further aspect, the one or more tetrahydrouridine compound or derivative can be tetrahydrouridine or a tetrahydrouridine analog, such as tetrahydrouridine (THU), fluorinated tetrahydrouridine analogs and derivatives thereof.
Non-limiting examples of suitable fluorinated tetrahydrouridines are 2′-fluorinated tetrahydrouridine derivatives, including, but not limited to, at least one of the following:
Further non-limiting examples of suitable fluorinated tetrahydrouridines are difluorotetrahydrouridine derivatives such as 2′-fluoro-2′-deoxytetrahydrouridines derivatives, including, but not limited to, at least one of the following:
In an embodiment, disclosed are crystalline polymorphs of 5-aza-4′-thio-2′-deoxycytidine, wherein the crystalline polymorph has a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ. In a further embodiment, the crystalline polymorph has an X-ray powder diffraction pattern that is substantially similar to, or the same as, the X-ray powder diffraction pattern shown in
In an embodiment, disclosed are crystalline polymorphs of 5-aza-4′-thio-2′-deoxycytidine, wherein the crystalline polymorph has a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ. In a further embodiment, the crystalline polymorph has an X-ray powder diffraction pattern substantially similar to, or the same as, the X-ray powder diffraction pattern shown in
In various embodiments the crystalline polymorph is present in a pharmaceutical composition, together with a pharmaceutically acceptable carrier.
In an embodiment, disclosed are methods of making a disclosed crystalline polymorph, the method comprising subjecting aza-T-dCyd to one or more of solvent equilibration, evaporative crystallization, anti-solvent addition, thermocycling crystallization, sonication, and vapor diffusion into solution. In a further embodiment, the crystalline polymorph has a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ. In a further embodiment, the crystalline polymorph has a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ.
In an embodiment, the method comprises one and only one of solvent equilibration, evaporative crystallization, anti-solvent addition, thermocycling crystallization, sonication, and vapor diffusion into solution. In an embodiment, the method comprises exactly two of solvent equilibration, evaporative crystallization, anti-solvent addition, thermocycling crystallization, sonication, and vapor diffusion into solution. In an embodiment, the method comprises more than two of solvent equilibration, evaporative crystallization, anti-solvent addition, thermocycling crystallization, sonication, and vapor diffusion into solution.
In various aspects, the present disclosure relates pharmaceutical compositions comprising a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and at least one pharmaceutically acceptable excipient.
In a further aspect, the present disclosure relates pharmaceutical compositions comprising a therapeutically effective amount of a therapeutic agent, wherein the therapeutic agent is 5-aza-4′-thio-2′-deoxycytidine having a structure represented by the formula:
and, wherein the therapeutic agent is a crystalline polymorph selected from polymorph Form A and polymorph Form F; wherein polymorph Form A has a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ; and wherein polymorph Form F has a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ.
In a further aspect, the present disclosure relates pharmaceutical compositions comprising a therapeutically effective amount of a first therapeutic agent, wherein the first therapeutic agent is 5-aza-4′-thio-2′-deoxycytidine having a structure represented by the formula:
and, wherein the first therapeutic agent is a crystalline polymorph selected from polymorph Form A and polymorph Form F; wherein polymorph Form A has a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ; and wherein polymorph Form F has a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ; and optionally comprising a second therapeutic agent, wherein the second therapeutic agent is tetrahydrouridine, a 2′-fluorinated tetrahydrouridine derivative, a pharmaceutically acceptable salt thereof, or combinations thereof.
In a yet further aspect, the disclosed pharmaceutical compositions can be an orally available, low dose, fixed dose, delayed release combination product thus providing an easy-to-use product for a patient to use at home.
In a further aspect, the present disclosure relates to pharmaceutical compositions comprising a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a pharmaceutically acceptable salt thereof, and optionally at least one disclosed tetrahydrouridine compound or derivative, or a pharmaceutically acceptable salt thereof. As used herein, “pharmaceutically-acceptable carriers” means one or more of a pharmaceutically acceptable diluents, preservatives, antioxidants, solubilizers, emulsifiers, coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, and adjuvants. The disclosed pharmaceutical compositions can be conveniently presented in unit dosage form and prepared by any of the methods well known in the art of pharmacy and pharmaceutical sciences.
In a further aspect, the disclosed pharmaceutical compositions comprise a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph or a pharmaceutically acceptable salt thereof, and optionally at least one disclosed tetrahydrouridine compound or derivative, or a pharmaceutically acceptable salt thereof, optionally one or more other therapeutic agent, and optionally one or more adjuvant. The disclosed pharmaceutical compositions include those suitable for oral, rectal, topical, pulmonary, nasal, and parenteral administration, although the most suitable route in any given case will depend on the particular host, and nature and severity of the conditions for which the active ingredient is being administered. In a still further aspect, the disclosed pharmaceutical composition can be formulated to allow administration orally.
In various aspects, the present disclosure also relates to a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and, as active ingredient, a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a pharmaceutically acceptable salt, a hydrate thereof, a solvate thereof, a polymorph thereof, or a stereochemically isomeric form thereof, and optionally, at least one disclosed tetrahydrouridine compound or derivative, or a pharmaceutically acceptable salt, a hydrate thereof, a solvate thereof, a polymorph thereof, or a stereochemically isomeric form thereof. In a further aspect, a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a pharmaceutically acceptable salt, a hydrate thereof, a solvate thereof, a polymorph thereof, or a stereochemically isomeric form thereof, and optionally, at least one tetrahydrouridine compound or derivative, or a pharmaceutically acceptable salt, a hydrate thereof, a solvate thereof, a polymorph thereof, or a stereochemically isomeric form thereof, may be formulated into various pharmaceutical forms for administration purposes.
In an embodiment, disclosed are pharmaceutical compositions comprising an effective amount of: (a) a crystalline polymorph having a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ; or (b) a crystalline polymorph having a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ, and a pharmaceutically acceptable carrier. In a further embodiment, the crystalline polymorph has a powder X-ray diffraction pattern that contains peaks at about 8°, about 13°, about 15°, about 17°, about 19°, about 22°, about 23° about 26°, about 28°, about 29°, about 31°, about 33°, and about 37° 2θ. In a still further embodiment, the crystalline polymorph has a powder X-ray diffraction pattern that contains peaks at about 6°, about 12°, about 13°, about 14°, about 16°, about 18°, about 20°, about 21°, about 22°, about 26°, about 27°, about 29°, about 30°, about 33°, about 35°, about 36°, about 39°, and about 41° 2θ.
Pharmaceutical compositions of the present disclosure encompass any composition made by admixing the active ingredients and a pharmaceutically acceptable carrier. The carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g., oral administration. Thus, the pharmaceutical composition of the invention can be presented as discrete units suitable for oral administration such as capsules, cachets or tablets each containing a predetermined amount of the active ingredients. Further, the composition can be presented as a powder, as granules, as a solution, as a suspension in an aqueous liquid, as a non-aqueous liquid, as an oil-in-water emulsion or as a water-in-oil liquid emulsion. In addition to the common dosage forms set out above, the composition may also be administered by controlled release means and/or delivery devices. The foregoing list is illustrative only and is not intended to be limiting in any way.
Pharmaceutically acceptable salts can be prepared from pharmaceutically acceptable non-toxic bases or acids. For therapeutic use, salts of the disclosed therapeutic agents are those wherein the counter ion is pharmaceutically acceptable. However, salts of acids and bases which are non-pharmaceutically acceptable may also find use, for example, in the preparation or purification of a pharmaceutically acceptable compound. All salts, whether pharmaceutically acceptable or not, are contemplated by the present disclosure. Pharmaceutically acceptable acid and base addition salts are meant to comprise the therapeutically active non-toxic acid and base addition salt forms which the disclosed compounds are able to form.
In various aspects, a disclosed therapeutic agent comprising an acidic group or moiety, e.g., a carboxylic acid group, can be used to prepare a pharmaceutically acceptable salt. For example, such a disclosed therapeutic agent may comprise an isolation step comprising treatment with a suitable inorganic or organic base. In some cases, it may be desirable in practice to initially isolate a compound from the reaction mixture as a pharmaceutically unacceptable salt and then simply convert the latter back to the free acid compound by treatment with an acidic reagent, and subsequently convert the free acid to a pharmaceutically acceptable base addition salt. These base addition salts can be readily prepared using conventional techniques, e.g., by treating the corresponding acidic compounds with an aqueous solution containing the desired pharmacologically acceptable cations and then evaporating the resulting solution to dryness, preferably under reduced pressure. Alternatively, they also can be prepared by mixing lower alkanolic solutions of the acidic compounds and the desired alkali metal alkoxide together, and then evaporating the resulting solution to dryness in the same manner as before.
Bases which can be used to prepare the pharmaceutically acceptable base-addition salts of the base therapeutic agents are those which can form non-toxic base-addition salts, i.e., salts containing pharmacologically acceptable cations such as, alkali metal cations (e.g., lithium, potassium and sodium), alkaline earth metal cations (e.g., calcium and magnesium), ammonium or other water-soluble amine addition salts such as N-methylglucamine-(meglumine), lower alkanolammonium and other such bases of organic amines. In a further aspect, derived from pharmaceutically acceptable organic non-toxic bases include primary, secondary, and tertiary amines, as well as cyclic amines and substituted amines such as naturally occurring and synthesized substituted amines. In various aspects, such pharmaceutically acceptable organic non-toxic bases include, but are not limited to, ammonia, methylamine, ethylamine, propylamine, isopropylamine, any of the four butylamine isomers, betaine, caffeine, choline, dimethylamine, diethylamine, diethanolamine, dipropylamine, diisopropylamine, di-n-butylamine, N,N′-dibenzylethylenediamine, pyrrolidine, piperidine, morpholine, trimethylamine, triethylamine, tripropylamine, tromethamine, 2-diethylaminoethanol, 2-dimethylaminoethanol, ethanolamine, quinuclidine, pyridine, quinoline and isoquinoline; benzathine, N-methyl-D-glucamine, ethylenediamine, N-ethylmorpholine, N-ethylpiperidine, glucamine, glucosamine, methylglucamine, morpholine, piperazine, piperidine, polyamine resins, procaine, purines, theobromine, hydrabamine salts, and salts with amino acids such as, for example, histidine, arginine, lysine and the like. The foregoing salt forms can be converted by treatment with acid back into the free acid form.
In various aspects, a disclosed therapeutic agent comprising a protonatable group or moiety, e.g., an amino group, can be used to prepare a pharmaceutically acceptable salt. For example, such a disclosed therapeutic agent may comprise an isolation step comprising treatment with a suitable inorganic or organic acid. In some cases, it may be desirable in practice to initially isolate a compound from the reaction mixture as a pharmaceutically unacceptable salt and then simply convert the latter back to the free base compound by treatment with a basic reagent, and subsequently convert the free base to a pharmaceutically acceptable acid addition salt. These acid addition salts can be readily prepared using conventional techniques, e.g., by treating the corresponding basic compounds with an aqueous solution containing the desired pharmacologically acceptable anions and then evaporating the resulting solution to dryness, preferably under reduced pressure. Alternatively, they also can be prepared by treating the free base form of the disclosed compound with a suitable pharmaceutically acceptable non-toxic inorganic or organic acid.
Acids which can be used to prepare the pharmaceutically acceptable acid-addition salts of the base therapeutic agent are those which can form non-toxic acid-addition salts, i.e., salts containing pharmacologically acceptable anions formed from their corresponding inorganic and organic acids. Exemplary, but non-limiting, inorganic acids include hydrochloric hydrobromic, sulfuric, nitric, phosphoric and the like. Exemplary, but non-limiting, organic acids include acetic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethanesulfonic, fumaric, gluconic, glutamic, isethionic, lactic, maleic, malic, mandelicmethanesulfonic, mucic, pamoic, pantothenic, succinic, tartaric, p-toluenesulfonic acid and the like. In a further aspect, the acid-addition salt comprises an anion formed from hydrobromic, hydrochloric, maleic, phosphoric, sulfuric, and tartaric acids.
In practice, the therapeutic agents of the present disclosure, or pharmaceutically acceptable salts thereof, of the present disclosure can be combined as the active ingredient in intimate admixture with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques. The carrier can take a wide variety of forms depending on the form of preparation desired for administration, e.g., oral or parenteral (including intravenous). Thus, the pharmaceutical compositions of the present disclosure can be presented as discrete units suitable for oral administration such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient. Further, the compositions can be presented as a powder, as granules, as a solution, as a suspension in an aqueous liquid, as a non-aqueous liquid, as an oil-in-water emulsion or as a water-in-oil liquid emulsion. In addition to the common dosage forms set out above, the compounds of the present disclosure, and/or pharmaceutically acceptable salt(s) thereof, can also be administered by controlled release means and/or delivery devices. The compositions can be prepared by any of the methods of pharmacy. In general, such methods include a step of bringing into association the active ingredient with the carrier that constitutes one or more necessary ingredients. In general, the compositions are prepared by uniformly and intimately admixing the active ingredient with liquid carriers or finely divided solid carriers or both. The product can then be conveniently shaped into the desired presentation.
It is especially advantageous to formulate the disclosed pharmaceutical compositions in a single dosage form for ease of administration and uniformity of dosage.
The pharmaceutical compositions disclosed herein comprise a therapeutic agent of the present disclosure (or pharmaceutically acceptable salts thereof) as an active ingredient, a pharmaceutically acceptable carrier, and optionally one or more additional therapeutic agents. In various aspects, the disclosed pharmaceutical compositions can include a pharmaceutically acceptable carrier and a disclosed compound, or a pharmaceutically acceptable salt thereof. In a further aspect, a disclosed compound, or pharmaceutically acceptable salt thereof, can also be included in a pharmaceutical composition in combination with one or more other therapeutically active compounds. The instant compositions include compositions suitable for oral administration, although the most suitable route in any given case will depend on the particular host, and nature and severity of the conditions for which the active ingredient is being administered. The pharmaceutical compositions can be conveniently presented in unit dosage form and prepared by any of the methods well known in the art of pharmacy.
Pharmaceutical compositions of the present disclosure may be prepared by any of the methods well known in the art of pharmacy. Techniques and compositions for making dosage forms useful for materials and methods described herein are described, for example, in the following references: Modern Pharmaceutics, Chapters 9 and 10 (Banker & Rhodes, Editors, 1979); Pharmaceutical Dosage Forms: Tablets (Lieberman et al., 1981); Ansel, Introduction to Pharmaceutical Dosage Forms 2nd Edition (1976); Remington's Pharmaceutical Sciences, 17th ed. (Mack Publishing Company, Easton, Pa., 1985); Advances in Pharmaceutical Sciences (David Ganderton, Trevor Jones, Eds., 1992); Advances in Pharmaceutical Sciences Vol 7. (David Ganderton, Trevor Jones, James McGinity, Eds., 1995); Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms (Drugs and the Pharmaceutical Sciences, Series 36 (James McGinity, Ed., 1989); Pharmaceutical Particulate Carriers: Therapeutic Applications: Drugs and the Pharmaceutical Sciences, Vol 61 (Alain Rolland, Ed., 1993); Drug Delivery to the Gastrointestinal Tract (Ellis Horwood Books in the Biological Sciences. Series in Pharmaceutical Technology; J. G. Hardy, S. S. Davis, Clive G. Wilson, Eds.); Modern Pharmaceutics Drugs and the Pharmaceutical Sciences, Vol 40 (Gilbert S. Banker, Christopher T. Rhodes, Eds.).
The therapeutic agents described herein are typically to be administered in admixture with suitable pharmaceutical diluents, excipients, extenders, or carriers (termed herein as a pharmaceutically acceptable carrier, or a carrier) suitably selected with respect to the intended form of administration and as consistent with conventional pharmaceutical practices. The deliverable compound will be in a form suitable for oral, rectal, topical, intravenous injection or parenteral administration. Carriers include solids or liquids, and the type of carrier is chosen based on the type of administration being used. The compounds may be administered as a dosage that has a known quantity of the compound.
Because of the ease in administration, oral administration can be a preferred dosage form for the disclosed pharmaceutical compositions, and tablets and capsules represent the most advantageous oral dosage unit forms in which case solid pharmaceutical carriers are obviously employed. However, other dosage forms may be suitable depending upon clinical population (e.g., age and severity of clinical condition), solubility properties of the specific disclosed compound used, and the like. Accordingly, the disclosed compounds can be used in oral dosage forms such as pills, powders, granules, elixirs, tinctures, suspensions, syrups, and emulsions. In preparing the compositions for oral dosage form, any convenient pharmaceutical media can be employed. For example, water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like can be used to form oral liquid preparations such as suspensions, elixirs and solutions; while carriers such as starches, sugars, microcrystalline cellulose, diluents, granulating agents, lubricants, binders, disintegrating agents, and the like can be used to form oral solid preparations such as powders, capsules and tablets. Because of their ease of administration, tablets and capsules are the preferred oral dosage units whereby solid pharmaceutical carriers are employed. Optionally, tablets can be coated by standard aqueous or nonaqueous techniques.
The disclosed pharmaceutical compositions in an oral dosage form can comprise one or more pharmaceutical excipient and/or additive. Non-limiting examples of suitable excipients and additives include gelatin, natural sugars such as raw sugar or lactose, lecithin, pectin, starches (for example corn starch or amylose), dextran, polyvinyl pyrrolidone, polyvinyl acetate, gum arabic, alginic acid, tylose, talcum, lycopodium, silica gel (for example colloidal), cellulose, cellulose derivatives (for example cellulose ethers in which the cellulose hydroxy groups are partially etherified with lower saturated aliphatic alcohols and/or lower saturated, aliphatic oxyalcohols, for example methyl oxypropyl cellulose, methyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl methyl cellulose phthalate), fatty acids as well as magnesium, calcium or aluminum salts of fatty acids with 12 to 22 carbon atoms, in particular saturated (for example stearates), emulsifiers, oils and fats, in particular vegetable (for example, peanut oil, castor oil, olive oil, sesame oil, cottonseed oil, corn oil, wheat germ oil, sunflower seed oil, cod liver oil, in each case also optionally hydrated); glycerol esters and polyglycerol esters of saturated fatty acids C12H24O2 to C18H36O2 and their mixtures, it being possible for the glycerol hydroxy groups to be totally or also only partly esterified (for example mono-, di- and triglycerides); pharmaceutically acceptable mono- or multivalent alcohols and polyglycols such as polyethylene glycol and derivatives thereof, esters of aliphatic saturated or unsaturated fatty acids (2 to 22 carbon atoms, in particular 10-18 carbon atoms) with monovalent aliphatic alcohols (1 to 20 carbon atoms) or multivalent alcohols such as glycols, glycerol, diethylene glycol, pentacrythritol, sorbitol, mannitol and the like, which may optionally also be etherified, esters of citric acid with primary alcohols, acetic acid, urea, benzyl benzoate, dioxolanes, glyceroformals, tetrahydrofurfuryl alcohol, polyglycol ethers with C1-C12-alcohols, dimethylacetamide, lactamides, lactates, ethylcarbonates, silicones (in particular medium-viscous polydimethyl siloxanes), calcium carbonate, sodium carbonate, calcium phosphate, sodium phosphate, magnesium carbonate and the like. In some aspects, the pharmaceutically acceptable excipient can be mannitol, microcrystalline cellulose, crospovidone, magnesium stearate, another excipient as disclosed herein, or a combination thereof.
Other auxiliary substances useful in preparing an oral dosage form are those which cause disintegration (so-called disintegrants), such as: cross-linked polyvinyl pyrrolidone, sodium carboxymethyl starch, sodium carboxymethyl cellulose or microcrystalline cellulose. Conventional coating substances may also be used to produce the oral dosage form. Those that may for example be considered are: polymerizates as well as copolymerizates of acrylic acid and/or methacrylic acid and/or their esters; copolymerizates of acrylic and methacrylic acid esters with a lower ammonium group content (for example EudragitR RS), copolymerizates of acrylic and methacrylic acid esters and trimethyl ammonium methacrylate (for example EudragitR RL); polyvinyl acetate; fats, oils, waxes, fatty alcohols; hydroxypropyl methyl cellulose phthalate or acetate succinate; cellulose acetate phthalate, starch acetate phthalate as well as polyvinyl acetate phthalate, carboxy methyl cellulose; methyl cellulose phthalate, methyl cellulose succinate, -phthalate succinate as well as methyl cellulose phthalic acid half ester; zein; ethyl cellulose as well as ethyl cellulose succinate; shellac, gluten; ethylcarboxyethyl cellulose; ethacrylate-maleic acid anhydride copolymer; maleic acid anhydride-vinyl methyl ether copolymer; styrol-maleic acid copolymerizate; 2-ethyl-hexyl-acrylate maleic acid anhydride; crotonic acid-vinyl acetate copolymer; glutaminic acid/glutamic acid ester copolymer; carboxymethylethylcellulose glycerol monooctanoate; cellulose acetate succinate; polyarginine.
Plasticizing agents that may be considered as coating substances in the disclosed oral dosage forms are: citric and tartaric acid esters (acetyl-triethyl citrate, acetyl tributyl-, tributyl-, triethyl-citrate); glycerol and glycerol esters (glycerol diacetate, -triacetate, acetylated monoglycerides, castor oil); phthalic acid esters (dibutyl-, diamyl-, diethyl-, dimethyl-, dipropyl-phthalate), di-(2-methoxy- or 2-ethoxyethyl)-phthalate, ethylphthalyl glycolate, butylphthalylethyl glycolate and butylglycolate; alcohols (propylene glycol, polyethylene glycol of various chain lengths), adipates (diethyladipate, di-(2-methoxy- or 2-ethoxyethyl)-adipate; benzophenone; diethyl- and diburylsebacate, dibutylsuccinate, dibutyltartrate; diethylene glycol dipropionate; ethyleneglycol diacetate, -dibutyrate, -dipropionate; tributyl phosphate, tributyrin; polyethylene glycol sorbitan monooleate (polysorbates such as Polysorbar 50); sorbitan monooleate.
Moreover, suitable binders, lubricants, disintegrating agents, coloring agents, flavoring agents, flow-inducing agents, and melting agents may be included as carriers. The pharmaceutical carrier employed can be, for example, a solid, liquid, or gas. Examples of solid carriers include, but are not limited to, lactose, terra alba, sucrose, glucose, methylcellulose, dicalcium phosphate, calcium sulfate, mannitol, sorbitol talc, starch, gelatin, agar, pectin, acacia, magnesium stearate, and stearic acid. Examples of liquid carriers are sugar syrup, peanut oil, olive oil, and water. Examples of gaseous carriers include carbon dioxide and nitrogen.
In various aspects, a binder can include, for example, starch, gelatin, natural sugars such as glucose or beta-lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth, or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes, and the like. Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride, and the like. In a further aspect, a disintegrator can include, for example, starch, methyl cellulose, agar, bentonite, xanthan gum, and the like.
In various aspects, an oral dosage form, such as a solid dosage form, can comprise a disclosed therapeutic agent that is attached to polymers as targetable drug carriers or as a prodrug. Suitable biodegradable polymers useful in achieving controlled release of a drug include, for example, polylactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, caprolactones, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and hydrogels, preferably covalently crosslinked hydrogels.
Tablets may contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients may be, for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example starch, gelatin or acacia, and lubricating agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period.
A tablet containing a disclosed compound can be prepared by compression or molding, optionally with one or more accessory ingredients or adjuvants. Compressed tablets can be prepared by compressing, in a suitable machine, the active ingredient in a free-flowing form such as powder or granules, optionally mixed with a binder, lubricant, inert diluent, surface active or dispersing agent. Molded tablets can be made by molding in a suitable machine, a mixture of the powdered compound moistened with an inert liquid diluent.
In various aspects, a solid oral dosage form, such as a tablet, can be coated with an enteric coating to prevent ready decomposition in the stomach. In various aspects, enteric coating agents include, but are not limited to, hydroxypropylmethylcellulose phthalate, methacrylic acid-methacrylic acid ester copolymer, polyvinyl acetate-phthalate and cellulose acetate phthalate. Akihiko Hasegawa “Application of solid dispersions of Nifedipine with enteric coating agent to prepare a sustained-release dosage form” Chem. Pharm. Bull. 33:1615-1619 (1985). Various enteric coating materials may be selected on the basis of testing to achieve an enteric coated dosage form designed ab initio to have a preferable combination of dissolution time, coating thicknesses and diametral crushing strength (e.g., see S. C. Porter et al. “The Properties of Enteric Tablet Coatings Made From Polyvinyl Acetate-phthalate and Cellulose acetate Phthalate”, J. Pharm. Pharmacol. 22:42p (1970)). In a further aspect, the enteric coating may comprise hydroxypropyl-methylcellulose phthalate, methacrylic acid-methacrylic acid ester copolymer, polyvinyl acetate-phthalate and cellulose acetate phthalate.
In various aspects, an oral dosage form can be a solid dispersion with a water soluble or a water insoluble carrier. Examples of water soluble or water insoluble carrier include, but are not limited to, polyethylene glycol, polyvinylpyrrolidone, hydroxypropylmethyl-cellulose, phosphatidylcholine, polyoxyethylene hydrogenated castor oil, hydroxypropylmethylcellulose phthalate, carboxymethylethylcellulose, or hydroxypropylmethylcellulose, ethyl cellulose, or stearic acid.
In various aspects, an oral dosage form can be in a liquid dosage form, including those that are ingested, or alternatively, administered as a mouth wash or gargle. For example, a liquid dosage form can include aqueous suspensions, which contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions. In addition, oily suspensions may be formulated by suspending the active ingredient in a vegetable oil, for example arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. Oily suspensions may also contain various excipients. The pharmaceutical compositions of the present disclosure may also be in the form of oil-in-water emulsions, which may also contain excipients such as sweetening and flavoring agents.
For the preparation of solutions or suspensions it is, for example, possible to use water, particularly sterile water, or physiologically acceptable organic solvents, such as alcohols (ethanol, propanol, isopropanol, 1,2-propylene glycol, polyglycols and their derivatives, fatty alcohols, partial esters of glycerol), oils (for example peanut oil, olive oil, sesame oil, almond oil, sunflower oil, soya bean oil, castor oil, bovine hoof oil), paraffins, dimethyl sulphoxide, triglycerides and the like.
In the case of a liquid dosage form such as a drinkable solutions, the following substances may be used as stabilizers or solubilizers: lower aliphatic mono- and multivalent alcohols with 2-4 carbon atoms, such as ethanol, n-propanol, glycerol, polyethylene glycols with molecular weights between 200-600 (for example 1 to 40% aqueous solution), diethylene glycol monoethyl ether, 1,2-propylene glycol, organic amides, for example amides of aliphatic C1-C6-carboxylic acids with ammonia or primary, secondary or tertiary C1-C4-amines or C1-C4-hydroxy amines such as urea, urethane, acetamide, N-methyl acetamide, N,N-diethyl acetamide, N,N-dimethyl acetamide, lower aliphatic amines and diamines with 2-6 carbon atoms, such as ethylene diamine, hydroxyethyl theophylline, tromethamine (for example as 0.1 to 20% aqueous solution), aliphatic amino acids.
In preparing the disclosed liquid dosage form can comprise solubilizers and emulsifiers such as the following non-limiting examples can be used: polyvinyl pyrrolidone, sorbitan fatty acid esters such as sorbitan trioleate, phosphatides such as lecithin, acacia, tragacanth, polyoxyethylated sorbitan monooleate and other ethoxylated fatty acid esters of sorbitan, polyoxyethylated fats, polyoxyethylated oleotriglycerides, linolizated oleotriglycerides, polyethylene oxide condensation products of fatty alcohols, alkylphenols or fatty acids or also 1-methyl-3-(2-hydroxyethyl)imidazolidone-(2). In this context, polyoxyethylated means that the substances in question contain polyoxyethylene chains, the degree of polymerization of which generally lies between 2 and 40 and in particular between 10 and 20. Polyoxyethylated substances of this kind may for example be obtained by reaction of hydroxyl group-containing compounds (for example mono- or diglycerides or unsaturated compounds such as those containing oleic acid radicals) with ethylene oxide (for example 40 Mol ethylene oxide per 1 Mol glyceride). Examples of oleotriglycerides are olive oil, peanut oil, castor oil, sesame oil, cottonseed oil, corn oil. See also Dr. H. P. Fiedler “Lexikon der Hillsstoffe für Pharmazie, Kostnetik und angrenzende Gebiete” 1971, pages 191-195.
In various aspects, a liquid dosage form can further comprise preservatives, stabilizers, buffer substances, flavor correcting agents, sweeteners, colorants, antioxidants and complex formers and the like. Complex formers which may be for example be considered are: chelate formers such as ethylene diamine retrascetic acid, nitrilotriacetic acid, diethylene triamine pentacetic acid and their salts.
It may optionally be necessary to stabilize a liquid dosage form with physiologically acceptable bases or buffers to a pH range of approximately 6 to 9. Preference may be given to as neutral or weakly basic a pH value as possible (up to pH 8).
In order to enhance the solubility and/or the stability of a disclosed compound in a disclosed liquid dosage form, a parenteral injection form, or an intravenous injectable form, it can be advantageous to employ α-, β- or γ-cyclodextrins or their derivatives, in particular hydroxyalkyl substituted cyclodextrins, e.g. 2-hydroxypropyl-β-cyclodextrin or sulfobutyl-β-cyclodextrin. Also co-solvents such as alcohols may improve the solubility and/or the stability of the compounds according to the present disclosure in pharmaceutical compositions.
In various aspects, a disclosed liquid dosage form, a parenteral injection form, or an intravenous injectable form can further comprise liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine, or phosphatidylcholines.
Pharmaceutical compositions containing a compound of the present disclosure, and/or pharmaceutically acceptable salts thereof, can also be prepared in powder or liquid concentrate form.
The pharmaceutical composition (or formulation) may be packaged in a variety of ways. Generally, an article for distribution includes a container that contains the pharmaceutical composition in an appropriate form. Suitable containers are well known to those skilled in the art and include materials such as bottles (plastic and glass), sachets, foil blister packs, and the like. The container may also include a tamper proof assemblage to prevent indiscreet access to the contents of the package. In addition, the container typically has deposited thereon a label that describes the contents of the container and any appropriate warnings or instructions.
The disclosed pharmaceutical compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient. The pack may for example comprise metal or plastic foil, such as a blister pack. The pack or dispenser device may be accompanied by instructions for administration. The pack or dispenser may also be accompanied with a notice associated with the container in form prescribed by a governmental agency regulating the manufacture, use, or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the drug for human or veterinary administration. Such notice, for example, may be the labeling approved by the U.S. Food and Drug Administration for prescription drugs, or the approved product insert. Pharmaceutical compositions comprising a disclosed compound formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition.
The exact dosage and frequency of administration depends on the particular disclosed compound, a product of a disclosed method of making, a pharmaceutically acceptable salt, solvate, or polymorph thereof, a hydrate thereof, a solvate thereof, a polymorph thereof, or a stereochemically isomeric form thereof; the particular condition being treated and the severity of the condition being treated; various factors specific to the medical history of the subject to whom the dosage is administered such as the age; weight, sex, extent of disorder and general physical condition of the particular subject, as well as other medication the individual may be taking; as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the present disclosure.
In another aspect, the pharmaceutical composition further includes a coating. In some aspects, the coating is an enteric coating. In still another aspect, the coating can be a sugar coating, a film coating, a compression coating, or a combination thereof. In aspects where the coating is a film coating, it can be a cellulose ether polymer such as, for example, a hydroxypropyl methylcellulose, hydroxypropyl cellulose, or methylcellulose polymer or a combination thereof.
Depending on the particular dosage form, a disclosed pharmaceutical composition can comprise from 0.05 to 99% by weight, preferably from 0.1 to 70% by weight, more preferably from 0.1 to 50% by weight of the active ingredient, and, from 1 to 99.95% by weight, preferably from 30 to 99.9% by weight, more preferably from 50 to 99.9% by weight of a pharmaceutically acceptable carrier, all percentages being based on the total weight of the composition.
In a further aspect, the disclosed pharmaceutical composition can have a unit dose form comprising from about 0.01 to 1000 mg per kg patient body weight per day of a disclosed therapeutic agent and can be administered in single or multiple doses. In various aspects, the dosage level of a disclosed therapeutic agent will be about 0.1 to about 500 mg/kg per day, about 0.1 to 250 mg/kg per day, or about 0.5 to 100 mg/kg per day. A suitable dosage level of a disclosed therapeutic agent can be about 0.01 to 1000 mg/kg per day, about 0.01 to 500 mg/kg per day, about 0.01 to 250 mg/kg per day, about 0.05 to 100 mg/kg per day, or about 0.1 to 50 mg/kg per day. Within this range the dosage can be 0.05 to 0.5, 0.5 to 5.0 or 5.0 to 50 mg/kg per day. For oral administration, the disclosed pharmaceutical compositions can be provided in the form of tablets containing a disclosed therapeutic agent of from about 1.0 to about 1000 mg of the active ingredient, particularly 1.0, 5.0, 10, 15, 20, 25, 50, 75, 100, 150, 200, 250, 300, 400, 500, 600, 750, 800, 900 and 1000 mg of the active ingredient for the symptomatic adjustment of the dosage of the patient to be treated. In one aspect, the tablets contain 40, 400, or 1000 mg of a disclosed therapeutic agent. The unit dose form can be administered on a regimen of 1 to 4 times per day, preferably once or twice per day. The unit dose form can be adjusted to provide the optimal therapeutic response. In a still further aspect, the unit dose form is administered once per week or is administered 2-3 times per week.
Disclosed unit doses as described can be administered more than once a day, for example, 2, 3, 4, 5 or 6 times a day. In various aspects, such unit doses can be administered 1 or 2 times per day, so that the total dosage for a 70 kg adult is in the range of 0.001 to about 15 mg per kg weight of subject per administration. In a further aspect, dosage is 0.01 to about 1.5 mg per kg weight of subject per administration, and such therapy can extend for a number of weeks or months, and in some cases, years. It will be understood, however, that the specific dose level for any particular subject will depend on a variety of factors including the activity of the specific compound employed; the age, body weight, general health, sex and diet of the individual being treated; the time and route of administration; the rate of excretion; other drugs that have previously been administered; and the severity of the particular disease undergoing therapy, as is well understood by those of skill in the area.
A typical unit dose can be taken once a day, or can be taken multiple times per day, or can be one time-release capsule or tablet taken once a day and containing a proportionally higher content of active ingredient. Alternatively, the unit dose can be taken once per week or 2-3 times per week. The time-release effect can be obtained by capsule materials that dissolve at different pH values, by capsules that release slowly by osmotic pressure, or by any other known means of controlled release.
In a further aspect, the disclosed pharmaceutical composition has a unit dose form comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph analog from about 1 to about 60 mg, or disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph from about 1.5 to about 15 mg, or a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph in an amount of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, or about 60 mg, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect, the foregoing pharmaceutical composition is formulated for oral administration.
a further aspect, the disclosed pharmaceutical composition has a unit dose form comprising disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 1 to 600 mg per m2 patient body surface area per day and can be administered in single or multiple doses. In various aspects, the dosage level will be about 1 to about 500 mg/m2 per day, about 1 to 250 mg/m2 per day, or about 1 to 150 mg/m2 per day. A suitable dosage level can be about 1 to 600 mg/m2 per day, about 1 to 250 mg/m2 per day, about 1 to 150 mg/m2 per day, about 1 to 100 mg/m2 per day, or about 1 to 50 mg/m2 per day. Within this range the dosage can be 1 to 50, 50 to 100, 100 to 150, 150 to 250, or 250 to 500 mg/m2 per day. In a still further aspect, the disclosed pharmaceutical composition has a unit dose form comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 5 mg/m2 to about 135 mg/m2, or can be about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, or about 135 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect the dose of the cytidine analog is 134 mg/m2.
In a further aspect, a disclosed pharmaceutical composition comprises a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph in a unit dose that can be administered more than once a day, for example, 2, 3, 4, 5 or 6 times a day. In various aspects, a disclosed pharmaceutical composition comprises a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph in a unit dose that can be administered 1 or 2 times per day, so that the total dosage for a 70 kg adult is in the range of 0.001 to about 15 mg per kg weight of subject per administration. In a further aspect, a disclosed pharmaceutical composition comprises a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph in a unit dose that is 0.01 to about 1.5 mg per kg weight of subject per administration, and such therapy can extend for a number of weeks or months, and in some cases, years. It will be understood, however, that the specific dose level for any particular patient will depend on a variety of factors including the activity of the specific compound employed; the age, body weight, general health, sex and diet of the individual being treated; the time and route of administration; the rate of excretion; other drugs that have previously been administered; and the severity of the particular disease undergoing therapy, as is well understood by those of skill in the area.
In a further aspect, the disclosed pharmaceutical composition has a unit dose form comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph that when administered to a subject provides an area-under-the-curve value for the a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 100 ng·hr/mL to about 400 ng·hr/mL, or of about 100, 150, 200, 225, 250, 275, 300, 325, 350, 375, or about 400 ng·hr/mL, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect, the foregoing pharmaceutical composition is formulated for oral administration.
In a further aspect, the disclosed pharmaceutical composition has a unit dose form comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph that when administered to a subject a maximum plasma concentration of the a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph from about 0.005 to about 0.05 μM following administration to the subject, or of about 0.005, 0.005, 0.01, 0.025, or about 0.05 μM, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In another aspect, the disclosed pharmaceutical composition has a unit dose form comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph that when administered to a subject achieves a maximum plasma concentration at from about 60 minutes to about 180 minutes following administration to a subject, or at about 60, 75, 90, 105, 120, 135, 150, 165, or about 180 minutes following administration to a subject, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect, the foregoing pharmaceutical composition is formulated for oral administration.
In one aspect, the disclosed pharmaceutical compositions comprise a disclosed CDA inhibitor such as, for example, tetrahydrouridine, is administered by intravenous infusion or subcutaneous injection or the like, it can be administered in a dosage of from about 10 to about 500 mg/m2 of body surface area, or at about 10, 25, 50, 75, 100, 150, 200, 250, 300, 350, 400, 450, or about 500 mg/m2 of body surface area, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values.
In a further aspect, the disclosed pharmaceutical compositions comprise a disclosed CDA inhibitor that is administered in tablet or capsule form, the CDA inhibitor is administered in dosage of from about 1 to about 400 mg/kg of body weight, or at about 1, 5, 10, 15, 20, 25, 50, 75, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, or about 400 mg/kg of body weight, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values.
It can be necessary to use dosages outside these ranges in some cases as will be apparent to those skilled in the art. Further, it is noted that the clinician or treating physician will know how and when to start, interrupt, adjust, or terminate therapy in conjunction with individual patient response.
In a further aspect, the disclosed pharmaceutical composition can optionally further comprise a unit dose form comprising a therapeutically effective amount of at least one tetrahydrouridine analog for treating a subject. In a still further aspect, the disclosed pharmaceutical composition can optionally further comprise a unit dose form comprising at least one tetrahydrouridine analog at a therapeutically effective dose of from about 100 to about 600 mg/m2 or can be about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, or about 600 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a yet further aspect, the disclosed pharmaceutical composition can optionally further comprise a unit dose form comprising at least one tetrahydrouridine analog at a therapeutically effective dose of from about 50 to about 350 mg/m2, or can be about 50, 100, 150, 200, 250, 300, or about 350 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the combinatorial compositions disclosed herein can include 145 mg/m2 of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and 350 mg/m2 tetrahydrouridine.
In a still further aspect, the disclosed pharmaceutical composition has a unit dose form comprising at least one tetrahydrouridine analog that when administered to a subject is bioavailable from about 1 to about 180 minutes, or from about 15 to about 60 minutes, before a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or about 15, 30, 45, 60, 75, 90, 105, 120, 135, 150, 165, or about 180 minutes before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a yet further aspect, the at least one tetrahydrouridine analog is not acid stable and is encapsulated in an enteric coating in the formulations disclosed herein in order to preserve its activity when administered to the subject. In a further aspect, the enteric coating can be formulated such that extended release of at least one tetrahydrouridine analog is possible by means such as, for example, microencapsulation, embedding in a matrix of a single layer or of different layers, or the like.
In another aspect, the disclosed pharmaceutical composition is formulated such that the tetrahydrouridine or tetrahydrouridine derivative is released more quickly than the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph. In one aspect, “differential release” or “dual release” as used herein refers to the release at different time points of two or more active ingredients from a formulation containing more than one active ingredient or drug. In a further aspect, “differential” and “dual release” also refer to bioavailability of two or more active ingredients at different time points after administration by ingestion or other means.
As used herein, “bioavailable” refers to absorption and use by the body of an active ingredient in a pharmaceutical. Thus, an “orally bioavailable” drug can be taken by mouth and absorbed without being destroyed in the digestive tract. In one aspect, the combinatorial compositions disclosed herein can produce at least about 10-fold improvement in the oral bioavailability of cytidine analog and tetrahydrouridine analog. In a further aspect, the combinatorial compositions exhibit low Cmax and a multi-hour Tmax, thus resulting in non-cytotoxic DNMT1 depletion by the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph. In a further aspect, the combinatorial compositions can result in peak cytidine analog concentrations of from about 0.05μπI to about 0.5μπI in a human subject, or of about 0.05, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, or about 0.5μπI in a human subject, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values.
In one aspect, in order to accomplish differential release with faster release of tetrahydrouridine or a tetrahydrouridine analog, the tetrahydrouridine or analog can be located at the surface of an oral administration form such as a tablet, for example, as an outer layer. In an alternative aspect, binders, excipients, fillers, coatings, and the like, can be formulated to allow for different dissolution rates for the tetrahydrouridine or analog as opposed to the cytidine analog. Further in this aspect, the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph can be located at the center of an oral administration form, or the binders, excipients, fillers, coatings, and the like for the cytidine analog portion of the oral administration form can be formulated to allow for a slower dissolution rate. In some aspects, the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph can be coated with or embedded in a polymer to facilitate delayed release. In one aspect, the tetrahydrouridine or tetrahydrouridine analog is bioavailable from about 1 minute to about 180 minutes before the cytidine analog, or from about 15 minutes to about 60 minutes before the cytidine analog, or from about 30 minutes to about 60 minutes before the cytidine analog, or about 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, or about 180 minutes before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a combination of the foregoing values, or a range encompassing any of the foregoing values. In an alternative aspect, the tetrahydrouridine or tetrahydrouridine analog can be formulated in a separate dosage form (e.g., pill, tablet, capsule, etc.) from the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, which can be administered separately. In some aspects, the active ingredients disclosed herein can be packaged in microspheres and/or microparticles, including microspheres and/or microparticles having different matrices with different dissolution rates such that delayed release is facilitated.
In a further aspect, delayed release can be accomplished with a matrix or coating that includes or consists of a poorly soluble polymer. In a further aspect, the poorly soluble polymer can be polyvinyl chloride, polyethylene, a vinyl polymer or copolymer, hydroxypropyl methyl cellulose, shellac, ammoniated shellac, shellac-acetyl alcohol, shellac n-butyl stearate, copolymers of acrylic and methacrylic acid esters having low content of quaternary ammonium groups, and combinations thereof. In some aspects, the vinyl polymers and/or copolymers can be polyvinyl pyrrolidone, polyvinyl acetate, polyvinylacetate phthalate, vinylacetate crotonic acid copolymer, ethylene-vinyl acetate copolymer, and combinations thereof.
In a further aspect, the disclosed pharmaceutical compositions can comprise at least one 2′-deoxycytidine analog and at least one fetal hemoglobin expression inducer, and optionally at least one tetrahydrouridine analog. In a further aspect, the disclosed pharmaceutical composition can comprise at least one 2′-deoxycytidine analog and at least one fetal hemoglobin inducer, and at least one tetrahydrouridine analog.
In one aspect, disclosed herein is a method for treating a hematological disorder in a subject, the method comprising administering a therapeutically effective amount of a disclosed pharmaceutical composition or a disclosed therapeutic agent to a subject. In a further aspect, the method comprises administering a therapeutically effective amount of a disclosed pharmaceutical composition comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph. In a still further aspect, the method comprises administering a disclosed pharmaceutical composition comprising a therapeutically effective amount of comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and a therapeutically effective amount of a tetrahydrouridine compound or analog.
In a further aspect, the method for treating a hematological disorder further comprises the step of identifying a subject having a hematological disorder. In a yet further aspect, the subject in the method for treating a hematological disorder has already been identified as having a hematological disorder. In a still further aspect, the hematological disorder can be sickle cell disease or thalassemia.
In a further aspect, the method for treating a hematological disorder comprises administering a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 0.1 to about 150 mg/m2, or can be from about 10 to about 150 mg/m2, or can be about 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, or about 150 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect,
In a further aspect, the method for treating a hematological disorder comprises administering a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 5 mg/m2 to about 135 mg/m2, or can be about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, or about 135 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a yet further aspect, the dose of the cytidine analog is 134 mg/m2.
In a further aspect, the method for treating a hematological disorder further comprises administering a therapeutically effective amount of a tetrahydrouridine analog to the subject. In a still further aspect, the therapeutically effective amount of the tetrahydrouridine analog can be from about 100 to about 600 mg/m2 or can be about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, or about 600 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a yet further aspect, the therapeutically effective amount of the tetrahydrouridine analog can be from about 50 to about 350 mg/m2, or can be about 50, 100, 150, 200, 250, 300, or about 350 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the combinatorial compositions disclosed herein can include 145 mg/m2 cytidine analog and 350 mg/m2 tetrahydrouridine.
In a further aspect, tetrahydrouridine is administered before administering the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, concurrently with the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or after the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph. In any of these aspects, the tetrahydrouridine is bioavailable from about 1 to about 180 minutes, or from about 15 to about 60 minutes, before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or about 15, 30, 45, 60, 75, 90, 105, 120, 135, 150, 165, or about 180 minutes before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In some aspects, tetrahydrouridine is not administered to the subject. In some aspects, the tetrahydrouridine is not acid stable and is encapsulated in an enteric coating in the formulations disclosed herein in order to preserve its activity when administered to the subject. In a further aspect, the enteric coating can be formulated such that extended release of tetrahydrouridine is possible by means such as, for example, microencapsulation, embedding in a matrix of a single layer or of different layers, or the like.
In one aspect, disclosed herein is a method for increasing fetal hemoglobin expression in a subject, the method comprising administering a therapeutically effective amount of a disclosed pharmaceutical composition or a disclosed therapeutic agent to a subject. In a further aspect, the method comprises administering a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and at least one HbF inducer. In a still further aspect, the method comprises administering a pharmaceutical composition comprising a therapeutically effective amount of a disclosed pharmaceutical composition comprising a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, at least on HbF inducer, and at least one at least one tetrahydrouridine analog.
In a further aspect, the method for increasing fetal hemoglobin expression further comprises the step of identifying a subject having a need for increasing fetal hemoglobin expression. In a yet further aspect, the subject in the method for increasing fetal hemoglobin expression has already been identified as having a need for increasing fetal hemoglobin expression.
In a further aspect, the need for increasing fetal hemoglobin expression is associated with a hemoglobinopathy. In a still further aspect, the method further comprises the step of identifying a subject having a hemoglobinopathy. In a yet further aspect, the subject has already been identified as having a hemoglobinopathy. In an even further aspect, the hemoglobinopathy is associated with sickle cell disease or thalassemia.
In a further aspect, the method for increasing fetal hemoglobin expression comprises administering a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 0.1 to about 150 mg/m2, or can be from about 10 to about 150 mg/m2, or can be about 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, or about 150 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect,
In a further aspect, the method for increasing fetal hemoglobin expression comprises administering a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from about 5 mg/m2 to about 135 mg/m2, or can be about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, or about 135 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a yet further aspect, the dose of the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph is 134 mg/m2. In a further aspect, the method for increasing fetal hemoglobin expression comprises administering a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph of from 0.1 to about 150 mg/m2, or can be from about 10 to about 150 mg/m2, or can be about 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, or about 150 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values.
In some aspects, the HbF inducer comprises one or more epigenetic modifiers as described herein can be administered in a therapeutically-effective or therapeutically synergistic amount. As used herein, a “therapeutically-effective amount” is an amount such that coadministration of the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and the one or more HbF inducers (which can include epigenetic modifiers), or administration of a single therapeutic composition or formulation including both classes of drug, as described herein, results in an increase or upregulation of HbF, or a results in inhibition of a blood disorder as disclosed herein, or both. Meanwhile, as used herein, a “therapeutically synergistic amount” is the amount of the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and the one or more HbF chemical inducers necessary to significantly reduce or eliminate conditions or symptoms associated with a blood disorder as disclosed herein, and/or to increase or upregulate HbF levels.
In a further aspect, the at least one HbF chemical inducer can be an epigenetic modifier such as, for example, at least one DNA methylation inhibitor, at least one histone deacetylase (HDAC) inhibitor, at least one DNA methylation inhibitor, at least one PK2 inhibitor, or a combinations thereof, that can increase HbF levels in hematopoietic progenitor cells. In a further aspect, the DNA methylation inhibitor can be 5-aza-2′-deoxycytidine. In another aspect, the HDAC inhibitor can be selected from suberoylanilide hydroxamic acid (SAHA, also marketed as Vorinostat), amide analogues of trichostatin A, hydroxamic acid analogs of trapoxin, and scriptaid (6-(1,3-Dioxo-1H, 3H-benzo[de]isoquinolin-2-yl)-hexanoic acid hydroxyamide) and analogs.
In a further aspect, a first pharmaceutical composition can comprise a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and a second pharmaceutical composition can comprise a HbF chemical inducer, and the first and second pharmaceutical compositions can be coadministered. Coadministration can be sequentially or simultaneously.
In a further aspect, the method for increasing fetal hemoglobin expression further comprises administering a therapeutically effective amount of a tetrahydrouridine analog, to the subject. In a still further aspect, the therapeutically effective amount of the tetrahydrouridine analog can be from about 100 to about 600 mg/m2 or can be about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, or about 600 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a yet further aspect, the therapeutically effective amount of the tetrahydrouridine analog can be from about 50 to about 350 mg/m2, or can be about 50, 100, 150, 200, 250, 300, or about 350 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the combinatorial compositions disclosed herein can include 145 mg/m2 a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and 350 mg/m2 tetrahydrouridine.
In a further aspect, the method further comprises administering a therapeutically effective amount of tetrahydrouridine analog to the subject. In one aspect, the therapeutically effective amount of tetrahydrouridine can be from about 100 to about 600 mg/m2 or can be about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, or about 600 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In any of these aspects, the tetrahydrouridine is bioavailable from about 1 to about 180 minutes, or from about 15 to about 60 minutes, before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or about 15, 30, 45, 60, 75, 90, 105, 120, 135, 150, 165, or about 180 minutes before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In some aspects, tetrahydrouridine is not administered to the subject. In some aspects, the tetrahydrouridine is not acid stable and is encapsulated in an enteric coating in the formulations disclosed herein in order to preserve its activity when administered to the subject. In a further aspect, the enteric coating can be formulated such that extended release of tetrahydrouridine is possible by means such as, for example, microencapsulation, embedding in a matrix of a single layer or of different layers, or the like.
In a further aspect, tetrahydrouridine is administered before administering the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, concurrently with the 2′-deoxycytidine analog, or after the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph. In any of these aspects, the tetrahydrouridine is bioavailable from about 1 to about 180 minutes, or from about 15 to about 60 minutes, before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or about 15, 30, 45, 60, 75, 90, 105, 120, 135, 150, 165, or about 180 minutes before the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect, tetrahydrouridine is not administered to the subject. In a yet further aspect, the tetrahydrouridine is not acid stable and is encapsulated in an enteric coating in the formulations disclosed herein in order to preserve its activity when administered to the subject. In a further aspect, the enteric coating can be formulated such that extended release of tetrahydrouridine is possible by means such as, for example, microencapsulation, embedding in a matrix of a single layer or of different layers, or the like.
In one aspect, method for increasing total hemoglobin or fetal hemoglobin expression in a subject can comprise administration of an additional therapeutic agent such as a AN-233 a prodrug conjugate of butyric acid (BA) and 6-aminolevulinate (ALA), Janus kinase (JAK) inhibitor, hydroxyurea, a hemoglobin oxygen-affinity modulator such as, for example, voxelotor sold under the trade name OXBRYTA®, luspatercept sold under the trade name REBLOZYL®, a P-selectin binder such as, for example, crizanlizumab or inclacumab, a pyruvate kinase M2 activator such as, for example, AG348 or FT-4202, a PDE9 inhibitor such as, for example, IMR-687, an HDAC inhibitor, a stimulator of soluble guanylate cyclase such as, for example, olinciguat, an anti-hepcidin therapy such as for example, PGT-300 or siRNA-GaINAc, or the like. In another aspect, the additional therapy can be an iron chelator such as, for example, desferasirox (sold under the trade name EXIADE®) or deferiprone (sold under the trade name FERRIPROX®. In still another aspect, the additional therapy can be a gene therapy product including, but not limited to, ZYNTEGLO®, ARU-1801, EDIT-301, ST-400, CTX001, ET-01, or a combination thereof.
In one aspect, method for increasing total hemoglobin or fetal hemoglobin expression in a subject can comprise administration of an Gardos channel blocker selected from the group consisting of imidazole antimycotics, clotrimazole, metronidazole, econazole, arginine, Tram-34, harybdotoxin, nifedipine, 2,2-Bis(4-fluorophenyl)-N-methoxy-2-phenylacetamidine, 2-(2-Chlorophenyl)-2,2-diphenylacetaldehyde oxime, 2-(2-Chlorophenyl)-2,2-bis(4-fluorophenyl)-N-hydroxyacetamidine, 2,2,2-Tris(4-fluorophenyl)-N-hydroxyacetamidine, 2-(2-Fluorophenyl)-2-(4-fluorophenyl)-N-hydroxy-2-phenylacetamidine, phosphoric acid 3-(2-oxazolyl)-4-[3-(trifluoromethyl)phenylsulfonamido]phenyl monoester, N-[2-(4,5-Dihydrooxazol-2-yl)phenyl]-3-(trifluoromethyl)benzenesulfonamide, N-[4-Methoxy-2-(2-oxazolyl)phenyl]benzene sulfonamide, N-[4,5-Dimethoxy-2-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-3-(trifluoromethyl)benzenesulfonamide, N-[2-(2-Furyl)phenyl]-3-(trifluoromethyl)benzenesulfonamide, N-[4-Methyl-2-(2-oxazolyl)phenyl]-3-(trifluoromethyl)benzenesulfonamide and senicapoc, preferably senicapoc or Tram-34.
In various aspects, also disclosed herein are methods for increasing the amount of fetal hemoglobin in the blood of a subject, the method including the steps of administering to a subject (a) a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and (b) a therapeutically effective amount of tetrahydrouridine.
In some aspects, the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and the tetrahydrouridine are packaged in two separate dosage forms and administered simultaneously. In another aspect, the tetrahydrouridine is administered before or after the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph. In yet another aspect, the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and tetrahydrouridine are packaged in the same dosage form. Further in this aspect, the dosage form can be an oral dosage form such as, for example, a layered tablet, a tablet-in-tablet, a tablet-in-capsule, or a capsule-in-capsule. In any of these aspects, the dosage form enables fast release of the tetrahydrouridine and delayed release of the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph.
In any of these aspects, after administration of the formulations disclosed herein to a subject in need thereof, fetal hemoglobin level in the blood of the subject increases to at least 5, 7.5, 10, 12.5, 15, 17.5, or 20%, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values, compared to fetal hemoglobin levels in the subject prior to treatment. In another aspect, prior to performance of the method, the subject can have a fetal hemoglobin level of less than 1 g/dL, whereas after the performance of the method, the subject can have a fetal plus total hemoglobin level of greater than 1 g/dL. In some aspects, the fetal plus total hemoglobin level remains greater than 1 g/dL for at least 6 months.
In a further aspect, the present disclosure relates to kits comprising at least one disclosed compound, or a pharmaceutically acceptable salt, hydrate, solvate, or polymorph thereof, and one or more of: (a) a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph; (b) at least one agent known to treat a disorder associated with DNMT1 activity; (c) instructions for treating a disorder associated with DNMT1 activity; or (d) instructions for administering the compound in connection with another sickle cell disease or thalassemia therapy.
The disclosed compounds and/or pharmaceutical compositions comprising the disclosed compounds can conveniently be presented as a kit, whereby two or more components, which may be active or inactive ingredients, carriers, diluents, and the like, are provided with instructions for preparation of the actual dosage form by the patient or person administering the drug to the patient. Such kits may be provided with all necessary materials and ingredients contained therein, or they may contain instructions for using or making materials or components that must be obtained independently by the patient or person administering the drug to the patient. In further aspects, a kit can include optional components that aid in the administration of the unit dose to patients, such as vials for reconstituting powder forms, syringes for injection, customized IV delivery systems, inhalers, etc. Additionally, a kit can contain instructions for preparation and administration of the compositions. The kit can be manufactured as a single use unit dose for one patient, multiple uses for a particular patient (at a constant dose or in which the individual compounds may vary in potency as therapy progresses); or the kit may contain multiple doses suitable for administration to multiple patients (“bulk packaging”). The kit components may be assembled in cartons, blister packs, bottles, tubes, and the like.
In a further aspect, the disclosed kits can be packaged in a daily dosing regimen (e.g., packaged on cards, packaged with dosing cards, packaged on blisters or blow-molded plastics, etc.). Such packaging promotes products and increases patient compliance with drug regimens. Such packaging can also reduce patient confusion. The present invention also features such kits further containing instructions for use.
In a further aspect, the present disclosure also provides a pharmaceutical pack or kit comprising one or more containers filled with one or more of the ingredients of the pharmaceutical compositions of the invention. Associated with such container(s) can be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration.
In various aspects, the disclosed kits can also comprise compounds and/or products co-packaged, co-formulated, and/or co-delivered with other components. For example, a drug manufacturer, a drug reseller, a physician, a compounding shop, or a pharmacist can provide a kit comprising a disclosed compound and/or product and another component for delivery to a patient.
It is contemplated that the disclosed kits can be used in connection with the disclosed methods of making, the disclosed methods of using or treating, and/or the disclosed compositions.
In one aspect, disclosed herein is a kit for treating a hematological disorder or a disease associated with abnormal cell proliferation in a subject, the kit comprising a therapeutically effective amount of a disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and a therapeutically effective amount of tetrahydrouridine. In a further aspect, the therapeutically effective amount of the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph is from about 0.1 to about 150 mg\m2 or is about 10 to 150 mg/m2, or about 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, or about 150 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In another aspect, the therapeutically effective amount of the tetrahydrouridine is from about 100 to about 600 mg/m2, or is about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, or about 600 mg/m2, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values.
In one aspect, the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph and the tetrahydrouridine are packaged in two separate dosage forms (e.g., pills, tablets, lyophilized powders for resuspension and injection, etc.). In a further aspect, the two separate dosage forms can be the same or different (e.g., one tablet and one lyophilized powder for resuspension and injection). Further in this aspect, the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph can be administered before, concurrently with, or after the tetrahydrouridine. In another aspect, the 2′-deoxycytidine analog and the tetrahydrouridine are packaged in the same dosage form. In some aspects, when both ingredients are packaged in the same dosage form, that dosage form is selected from a layered tablet, a tablet-in-tablet form, a tablet-in-capsule form, a capsule-in-capsule form, or some combination thereof. In a further aspect, the single dosage form enables fast release of tetrahydrouridine and delayed release of the disclosed 5-aza-4′-thio-2′-deoxycytidine polymorph.
In any of the above aspects, the kit further comprises instructions on using the kit.
The disclosed compounds and pharmaceutical compositions have activity as inhibitors of DNMT1 As such, the disclosed compounds are also useful as research tools. Accordingly, one aspect of the present disclosure relates to a method of using a compound of the invention as a research tool, the method comprising conducting a biological assay using a compound of the invention. Compounds of the invention can also be used to evaluate new chemical compounds. Thus another aspect of the invention relates to a method of evaluating a test compound in a biological assay, comprising: (a) conducting a biological assay with a test compound to provide a first assay value; (b) conducting the biological assay with a compound of the invention to provide a second assay value; wherein step (a) is conducted either before, after or concurrently with step (b); and (c) comparing the first assay value from step (a) with the second assay value from step (b). Still another aspect of the invention relates to a method of studying a biological system, e.g., a model animal for a clinical condition, or biological sample comprising a DNMT1 protein, the method comprising: (a) contacting the biological system or sample with a compound of the invention; and (b) determining the effects caused by the compound on the biological system or sample.
The following listing of exemplary aspects supports and is supported by the disclosure provided herein.
Aspect 1. A pharmaceutical composition comprising a therapeutically effective amount of a compound of a first therapeutic agent, optionally a second therapeutic agent, and at least one pharmaceutically acceptable excipient; wherein the first therapeutic agent is 5-aza-4′-thio-2′-deoxycytidine, or a pharmaceutically acceptable salt thereof; and wherein the second therapeutic agent is tetrahydrouridine, a 2′-fluorinated tetrahydrouridine derivative, a pharmaceutically acceptable salt thereof, or combinations thereof; wherein the first therapeutic agent has the following structure:
and wherein the 5-aza-4′-thio-2′-deoxycytidine is a crystalline polymorph thereof as disclosed herein, including, but not limited to, polymorph Form A or polymorph Form F.
Aspect 2. The pharmaceutical composition of Aspect 1, wherein the second therapeutic agent is selected from tetrahydrouridine; 2′-Deoxy-2′,2′-difluoro-5,6-dihydrouridine; (4R)-2′-Deoxy-2′,2′-difluoro-3,4,5,6-tetrahydrouridine; (4S)-2′-Deoxy-2′,2′-difluoro-3,4,5,6-tetrahydrouridine; 1-(2-Deoxy-2,2-difluoro-β-D-erythro-pentofuranosyl)-tetrahydro-2(1H)-pyrimidinone; 2′-Deoxy-2′-fluoro-5,6-dihydrouridine; (4R)-2′-Deoxy-2′-fluoro-3,4,5,6-tetrahydrouridine; (4S)-2′-Deoxy-2′-fluoro-3,4,5,6-tetrahydrouridine; 1-(2-Deoxy-2-fluoro-(3-D-ribofuranosyl)tetra-hydro-2(1H)-pyrimidinone; 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)dihydro-2,4-(1H, 3H)-pyrimidinedione; (4R)-1-(2-Deoxy-2-fluoro-(3-D-arabinofuranosyl)tetrahydro-4-hydroxy-2(1H)-pyrimidinone; (4S)-1-(2-Deoxy-2-fluoro-(3-D-arabinofuranosyl)tetrahydro-4-hydroxy-2(1H)-pyrimidinone, a pharmaceutically acceptable salt thereof, or combinations thereof.
Aspect 3. The pharmaceutical composition of any of Aspect 1-Aspect 2, wherein the at least one pharmaceutically acceptable excipient comprises mannitol, microcrystalline cellulose, crospovidone, or magnesium stearate.
Aspect 4. The pharmaceutical composition of any of Aspect 1-Aspect 3, wherein the tetrahydrouridine (THU) is formulated as a enteric coated, stomach or gastric acid stable formulation.
Aspect 5. The pharmaceutical composition of any of Aspect 1-Aspect 4, wherein the first therapeutic agent is present in an amount of from about 1 mg to about 50 mg in a single dosage form.
Aspect 6. The pharmaceutical composition of any of Aspect 1-Aspect 5, wherein the pharmaceutical composition is administered orally.
Aspect 7. The pharmaceutical composition of Aspect 6, wherein the pharmaceutical composition for oral administration has a dosage form comprising a layered tablet, a tablet-in-tablet form, a tablet-in-capsule form, or a capsule-in-capsule form, granule, powder in sachet or bag, capsule, tablet, pill, or other oral solid dosage form.
Aspect 8. The pharmaceutical composition of any one of Aspect 1-Aspect 7, wherein the therapeutically effective amount of the second therapeutic agent comprises from about 100 to about 600 mg/m2.
Aspect 9. The pharmaceutical composition of any one of Aspect 1-Aspect 8, wherein the tetrahydrouridine analog is bioavailable from about 1 to about 60 minutes before the compound of formula I.
Aspect 10. A method for treating a hematological disorder in a subject, the method comprising administering a therapeutically effective amount of a compound of a first therapeutic agent, optionally a second therapeutic agent, and at least one pharmaceutically acceptable excipient; wherein the first therapeutic agent is 5-aza-4′-thio-2′-deoxycytidine, or a pharmaceutically acceptable salt thereof; and wherein the second therapeutic agent is tetrahydrouridine, a 2′-fluorinated tetrahydrouridine derivative, a pharmaceutically acceptable salt thereof, or combinations thereof; wherein the first therapeutic agent has the following structure:
and wherein the 5-aza-4′-thio-2′-deoxycytidine is a crystalline polymorph thereof as disclosed herein, including, but not limited to, polymorph Form A or polymorph Form F.
Aspect 11. The method of Aspect 10, wherein the hematological disorder comprises sickle cell disease or thalassemia or anemia.
Aspect 12. The method of any one of Aspect 10-Aspect 11, wherein the second therapeutic agent is selected from tetrahydrouridine; 2′-Deoxy-2′,2′-difluoro-5,6-dihydrouridine; (4R)-2′-Deoxy-2′,2′-difluoro-3,4,5,6-tetrahydrouridine; (4S)-2′-Deoxy-2′,2′-difluoro-3,4,5,6-tetrahydrouridine; 1-(2-Deoxy-2,2-difluoro-β-D-erythro-pentofuranosyl)-tetrahydro-2(1H)-pyrimidinone; 2′-Deoxy-2′-fluoro-5,6-dihydrouridine; (4R)-2′-Deoxy-2′-fluoro-3,4,5,6-tetrahydrouridine; (4S)-2′-Deoxy-2′-fluoro-3,4,5,6-tetrahydrouridine; 1-(2-Deoxy-2-fluoro-(3-D-ribofuranosyl)tetra-hydro-2(1H)-pyrimidinone; 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)dihydro-2,4-(1H, 3H)-pyrimidinedione; (4R)-1-(2-Deoxy-2-fluoro-(3-D-arabinofuranosyl)tetrahydro-4-hydroxy-2(1H)-pyrimidinone; (4S)-1-(2-Deoxy-2-fluoro-(3-D-arabinofuranosyl)tetrahydro-4-hydroxy-2(1H)-pyrimidinone, a pharmaceutically acceptable salt thereof, or combinations thereof.
Aspect 13. The method of any one of Aspect 10-Aspect 12, wherein the first therapeutic agent and the second therapeutic agent are administered as the pharmaceutical composition of any one of Aspect 1-Aspect 12 to the subject.
Aspect 14. The method of any one of Aspect 10-Aspect 12, wherein the first therapeutic agent and the second therapeutic agent are administered sequentially or simultaneously.
Aspect 15. The method of any of Aspect 10-Aspect 14, wherein the subject is a human.
Aspect 16. The method of any of Aspect 10-Aspect 21, wherein the first therapeutic agent further comprises at least one at least one pharmaceutically acceptable excipient.
Aspect 17. The method of Aspect 22, wherein the at least one pharmaceutically acceptable excipient comprises mannitol, microcrystalline cellulose, crospovidone, or magnesium stearate.
Aspect 18. The method of any of Aspect 10-Aspect 17 wherein the second therapeutic agent further comprises at least one at least one pharmaceutically acceptable excipient.
Aspect 19. The method of Aspect 18, wherein the at least one pharmaceutically acceptable excipient comprises mannitol, microcrystalline cellulose, crospovidone, or magnesium stearate.
Aspect 20. The method of any of Aspect 10-Aspect 19, wherein the tetrahydrouridine (THU) is administered as an enteric coated, stomach or gastric acid stable formulation.
Aspect 21. The method of any of Aspect 10-Aspect 20, wherein the first therapeutic agent is administered in an amount of from about 1 mg to about 50 mg in a single dosage form.
Aspect 22. The method of any of Aspect 10-Aspect 21, wherein the first therapeutic agent is administered orally.
Aspect 23. The method of Aspect 22, wherein the first therapeutic agent is administered orally as a dosage form comprising a layered tablet, a tablet-in-tablet form, a tablet-in-capsule form, or a capsule-in-capsule form, granule, powder in sachet or bag, capsule, tablet, pill, or other oral solid dosage form.
Aspect 24. The method of any of Aspect 10-Aspect 23, wherein the second therapeutic agent is administered in an amount of from about 100 to about 600 mg/m2 in a single dosage form.
Aspect 25. The method of any of Aspect 10-Aspect 24, wherein the tetrahydrouridine analog is bioavailable from about 1 to about 60 minutes before the compound of formula I.
Aspect 26. A kit for treating a hematological disorder, increasing fetal hemoglobin, or a disease associated with abnormal cell proliferation in a subject, the kit comprising: (a) a therapeutically effective amount of a first therapeutic agent, wherein the first therapeutic agent is 5-aza-4′-thio-2′-deoxycytidine, or a pharmaceutically acceptable salt thereof, or combinations thereof; and (b) instructions for treating a hematological disorder in a subject; and optionally, (c) a therapeutically effective amount of a second therapeutic agent, wherein the second therapeutic agent is tetrahydrouridine, a 2′-fluorinated tetrahydrouridine derivative, a pharmaceutically acceptable salt thereof, or combinations thereof.
Aspect 27. The kit of Aspect 26, wherein the first therapeutic agent and the second therapeutic agent are packaged in two separate dosage or same dosage forms.
Aspect 28. The kit of Aspect 26, wherein the first therapeutic agent and the second therapeutic agent are packaged in the same dosage form.
Aspect 29. The kit of Aspect 28, wherein dosage form enables fast release of the second therapeutic agent and delayed release of the first therapeutic agent.
Aspect 30. The kit of any one of Aspect 26-Aspect 29, wherein the first therapeutic agent has the following structure:
or a crystalline polymorph thereof as disclosed herein, including, but not limited to, polymorph Form A or polymorph Form F.
Aspect 31. The kit of any one of Aspect 26-Aspect 30, wherein the second therapeutic agent is selected from tetrahydrouridine; 2′-Deoxy-2′,2′-difluoro-5,6-dihydrouridine; (4R)-2′-Deoxy-2′,2′-difluoro-3,4,5,6-tetrahydrouridine; (4S)-2′-Deoxy-2′,2′-difluoro-3,4,5,6-tetrahydrouridine; 1-(2-Deoxy-2,2-difluoro-β-D-erythro-pentofuranosyl)-tetrahydro-2(1H)-pyrimidinone; 2′-Deoxy-2′-fluoro-5,6-dihydrouridine; (4R)-2′-Deoxy-2′-fluoro-3,4,5,6-tetrahydrouridine; (4S)-2′-Deoxy-2′-fluoro-3,4,5,6-tetrahydrouridine; 1-(2-Deoxy-2-fluoro-(3-D-ribofuranosyl)tetra-hydro-2(1H)-pyrimidinone; 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)dihydro-2,4-(1H, 3H)-pyrimidinedione; (4R)-1-(2-Deoxy-2-fluoro-(3-D-arabinofuranosyl)tetrahydro-4-hydroxy-2(1H)-pyrimidinone; (4S)-1-(2-Deoxy-2-fluoro-(3-D-arabinofuranosyl)tetrahydro-4-hydroxy-2(1H)-pyrimidinone, a pharmaceutically acceptable salt thereof, or combinations thereof.
Aspect 32. The kit of any one of Aspect 26-Aspect 31, wherein the hematological disorder comprises sickle cell disease or thalassemia or anemia.
From the foregoing, it will be seen that aspects herein are well adapted to attain all the ends and objects hereinabove set forth together with other advantages which are obvious and which are inherent to the structure.
While specific elements and steps are discussed in connection to one another, it is understood that any element and/or steps provided herein is contemplated as being combinable with any other elements and/or steps regardless of explicit provision of the same while still being within the scope provided herein.
It will be understood that certain features and subcombinations are of utility and may be employed without reference to other features and subcombinations. This is contemplated by and is within the scope of the claims.
Since many possible aspects may be made without departing from the scope thereof, it is to be understood that all matter herein set forth or shown in the accompanying drawings and detailed description is to be interpreted as illustrative and not in a limiting sense.
Aspect 1: A method for treating a hematological disorder in a subject, the method comprising administering a therapeutic agent;
Aspect 2: The method of Aspect 1, wherein the hematological disorder comprises sickle cell disease, thalassemia, anemia, or combinations thereof.
Aspect 3: The method of Aspect 1 or Aspect 2, wherein the polymorph Form A exhibits an X-ray powder diffraction pattern that is substantially similar to, or the same as, the X-ray powder diffraction pattern shown in
Aspect 4: The method of any one of Aspects 1-3, wherein the polymorph Form F exhibits an X-ray powder diffraction pattern that is substantially similar to, or the same as, the X-ray powder diffraction pattern shown in
Aspect 5: The method of any one of Aspects 1-4, wherein the subject is a human.
Aspect 6: The method of any one of Aspects 1-5, wherein the therapeutic agent further comprises at least one at least one pharmaceutically acceptable excipient.
Aspect 7: The method of Aspect 6, wherein the at least one pharmaceutically acceptable excipient comprises mannitol, microcrystalline cellulose, crospovidone, or magnesium stearate.
Aspect 8: The method of any one of Aspects 1-7, wherein the therapeutic agent is administered in an amount of from about 1 mg to about 50 mg in a single dosage form.
Aspect 9: The method of any one of Aspects 1-8, wherein the therapeutic agent is administered orally.
It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to be limiting. The skilled artisan will recognize many variants and adaptations of the aspects described herein. These variants and adaptations are intended to be included in the teachings of this disclosure and to be encompassed by the claims herein.
Now having described the aspects of the present disclosure, in general, the following Examples describe some additional aspects of the present disclosure. While aspects of the present disclosure are described in connection with the following examples and the corresponding text and figures, there is no intent to limit aspects of the present disclosure to this description. On the contrary, the intent is to cover all alternatives, modifications, and equivalents included within the spirit and scope of the present disclosure.
The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how the compounds, compositions, articles, devices and/or methods claimed herein are made and evaluated, and are intended to be purely exemplary of the disclosure and are not intended to limit the scope of what the inventors regard as their disclosure. Efforts have been made to ensure accuracy with respect to numbers (e.g., amounts, temperature, etc.), but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in ° C. or is at ambient temperature, and pressure is at or near atmospheric.
Compounds of the present disclosure can be prepared according to methods described in Tiwari, K. N. et al., “Synthesis and anti-cancer activity of some novel 5-azacytosine nucleosides,” Nucleosides Nucleotides Nucleic Acids, 2003, 22:2161-2170, Secrist, J. A. et al., “Synthesis and biological activity of 2′-deoxy-4′-thio pyrimidine nucleosides,” J. Med. Chem., 1991, 34:2361-2366, U.S. Pat. No. 5,591,722 to Montgomery et al., European Patent 0 421 777 to Walker et al., and international patent application publication WO 2019152459 to Morris et al., each of which is incorporated herein by reference.
The following scheme illustrates synthesis of 5-aza-2′-deoxy-4′-thio cytidine and can be applied to other cytidine analogs using appropriate starting materials. Protecting groups can be removed by any method known in the art.
Example formulations for delivering the compounds disclosed herein are provided below.
An oral dosage form for administering a compound as disclosed herein is produced by filling a standard two-piece hard gelatin capsule with ingredients as follows: active compound 7 mg, lactose 53 mg, talc 16 mg, magnesium stearate 4 mg.
An injectable form for administering a compound as disclosed herein is produced by stirring 1.7% by weight of active compound in 10% by volume propylene glycol in water.
A tablet is prepared with the following ingredients: 12 mg of active compound, 30 mg of calcium sulfate dihydrate, 4 mg sucrose, 2 mg starch 1 mg talc, and 0.5 mg stearic acid. Sucrose, calcium sulfate dihydrate, and active compound are mixed and granulated in the proportions shown with a 10% gelatin solution. Wet granules are screened, dried, mixed with starch, talc, and stearic acid, screened again, and compressed into a tablet.
Day 7 EPCs are cultured in duplicate plates with serially diluted 2′-deoxycytidine analogs for 5 days at 37° C. Wells are then analyzed for either induction of fetal hemoglobin (HbF, HbF ELISA) or cell growth (Cell Titer-Glo). In both cases, the signal is normalized to vehicle-control treated cells. Ideal candidate compounds induced an increase in HbF with an average pEC50 of 6.5 and inhibited cell growth by 50% with an average pGI50 of 5.9.
To assay the effect of 2′-deoxycytidine analogs on DNA methylation, EPCs treated for 3 days with representative compounds are harvested and genomic DNA is bisulfite sequenced. Methylation of CpG sites in or near the promoter regions of HBG1 and HBG2 gene loci are selected and analyzed based on previous characterization as sites of DNMT1 methaylation during erythropoiesis. All sites showed reduction in methylation, averaging 65±5% decreases compared with vehicle-treated cells. Additional details on the experimental methods used for this assay are provided below.
All donors provided written informed consent for the use of their samples and the collection and use of samples received institutional review board approval. All cryopreserved human bone marrow CD34+ cells used herein are obtained from AllCells (Emeryville, Calif.) and are generally from different donors. The CD34+ cells are cultured to generate EPCs at day 7. Approximately 1,000,000 cells are cultured in 5% CO2, 5% O2 at 37° C. in H3000 Stemspan media (StemCell Technologies, Vancouver, BC, Canada) supplemented with 2 mM L-glutamine, 40 μg/mL human low-density lipoproteins (StemCell Technologies), 10 ng/mL recombinant human (rh) interleukin IL-3 (R&D Systems, Minneapolis, Minn.), 100 ng/mL rh stem cell factor (R&D Systems), and 0.5 U/mL rh erythropoietin (Invitrogen, Grand Island, N.Y.). Cells are split and refed on day 4 with the complete culture media described above and harvested on day 7 for evaluation of erythroid marker expression and assessment of γ-globin induction. Day 7 EPCs are then frozen in liquid nitrogen at 5-10 million cells/mL in 95% fetal bovine serum (FBS; Invitrogen) with 5% DMSO for subsequent use.
At the time of compound treatment, frozen day 7 EPCs prepared as described above are thawed, ished once, and re-suspended in complete culture media as described above with the exception of an increase of rhEPO to 3 U/mL. Cells are counted and diluted to 3.3×103 cells/mL for plating into assay plates. Cells are then dispensed at 30 μL per well with a Multidrop Combi Reagent Dispenser (Thermo Scientific) into 384-well culture plates into which test compounds had been pre-dispensed at 100 nL/well. Black Clear Bottom (Greiner Bio-One product 781090) and White (Greiner Bio-One product 781080) plates are used for ELISA and Cell Titer-Glo assays, respectively. The final cell density in the assays is 1000 cells per well, with final compound concentrations between 33 nM and 6.6 nM for a 22 point serial dilution.
To monitor cell health and cell growth, cell growth assays are performed at the time of cell plating (day 0) using Cell Titer-Glo (see below). For compound treatment, the cell culture plates are incubated for 5 days at 37° C. with 5% CO2.
Coating anti-HbF Ab (Bethyl Lab, product A80-136A) is diluted 100-fold in the coating buffer (0.05 M carbonate-bicarbonate at pH 9.6) and 20 μL/well is added to a 384-well MaxiSorp ELISA plate (Thermo Fisher product 464718). After 1 h incubation at room temperature, the plates are ished twice with ELISA ishing buffer (50 mM Tris and 0.05% polysorbate 20 at pH 8.0) with an EL406 plate isher (BioTek, Winooski, Vt.). 40 μL/well of blocking buffer (50 mM Tris and 1% BSA at pH 8.0) is added to the plate and stored at 4° C. with cover sheet overnight or until time of the assay. Coated ELISA plates are stable for up to 30 days at 4° C. On the day of the assay, plates are ished twice with ELISA ishing buffer prior to addition of cell lysate.
After 5 days at 37° C. with 5% CO2, cell culture plates for the ELISA assay are frozen at −80° C. for a minimum of 2 h. After thawing at room temperature, 30 μL of cell lysis buffer (Invitrogen product FNN0011 supplemented with 1× protease inhibitor) are added to each well and the resulting cell lysate is mixed eight times with a Cybi-Well (Jena, Germany) pipettor. Following the mixing procedure, 20μ/well of lysate is transferred to the coated ELISA plates described previously, followed by 1 h incubation at room temperature. The ELISA assay plates are then ished three times with ELISA ish buffer. 20 μL per well of 1:75,000 to 100,000 diluted horseradish peroxidase (HRP) conjugate detection antiHBF Ab (Bethyl Labs product A80-136P, diluted in 50 mM Tris at pH 8.0, 1% BSA, and 0.05% polysorbate 20) is then added. After another 1 h incubation at room temperature, plates are ished four times and 20 μL per well of tetramethyl benzidine ELISA substrate (Thermo Scientific product 34028) are added. After 3-10 min incubation at room temperature in the dark, 20 μL/well of stop solution (0.2 M H2SO4) are added. The plates are ten read at 450 nm with an Envision plate reader (Perkin Elmer, Waltham, Mass.). The average reading of the control wells (16 wells in column 6 of each assay plate) containing DMSO only are used as the base level for normalization. The γ-globin level of each compound-treated well is calculated as a percentage of the base level.
The normalized responses of 22 concentrations of each test compound are subjected to curve fitting using a customized statistical computing tool based on R (R Foundation for Statistical Computing). An EC50 value (compound concentration at ½ Max %) and the corresponding Max % are determined from fitted curves for each active compound.
Cell growth assays are performed on cell culture plates after days incubation at 37° C. with 5% CO2. 15 μL per well of Cell Titer-Glo (Promega, Madison, Wis.) assay reagent are added to the assay plates. The plates are then incubated at room temperature for 10 min prior to reading on a ViewLux 1430 (Perkin Elmer) using a luminescence protocol provided by the manufacturer. The average reading of control wells (16 wells in column 6 of each assay plate) containing DMSO only is used as the base level for normalization. The Cell Titer-Glo signal of each test well is calculated as a percentage of the base level. Normalized responses of the 22 concentrations of each test compound are subjected to curve fitting using a customized statistical computing tool based on R (R Foundation for Statistical Computing).
To monitor cell health and cell growth, the Cell Titer-Glo signal of DMSO control wells is compared to the signal obtained on day 0. For health cell growth, increase of approximately 20× is typically observed at day 5 compared to day 0.
It is anticipated that the disclosed compounds and formulations will show improved fetal hemoglobin inducer effect on erythroid progenitor cells in vitro in the foregoing erythroid progenitor cell assay compared to conventional compounds or formulations.
A mouse model of sickle cell disease is used to measure the in vivo efficacy of test compounds shown to have potent in vitro activity in human primary erythroid progenitor cells derived from normal bone marrow or sickle cell patient peripheral blood mononuclear cells.
Experiments are conducted in accordance with US/UK standards of animal care. Male and female human hemoglobin transgenic mice [B6; 129-Hbatm1(HBA)Tow/Hbbtm2(HBG1,HBB*)Tow/J Mice (Jackson Laboratories, ME)] are approximately 6-8 weeks old and weighed approximately 15-25 g at the initiation of the studies.
To the extent possible, groups are sex-balanced and contained 6 mice each.
Mice are administered vehicle (10% DMA/90% PEG400), 10 mg/kg test compound, or 50 mg/kg test compound twice daily (BID) by an oral route 5 days per week over a two week period. At the end of the dosing period, mice are euthanized by CO2 asphyxiation and blood from the vena cava is collected into EDTA tubes for fetal hemoglobin analysis. % HbF protein is determined by HPLC and % F cells (HbF expressing erythrocytes) is determined by flow cytometry. The mouse monoclonal anti-human HbF antibody conjugated to APC (Life Technologies, Grand Island, N.Y.) is used to identify HbF-expressing erythroid cells. Nuclear dye SYTO™ 16 (Life Technologies) is used to separate the reticulocyte and RBC populations. Protein and cellular data are collected on a Bio-Rad D10 analyzer (Bio-Rad, Benicia, Calif.) and an FACs Canto I (BD BioSciences, San Jose, Calif.), respectively. Flow cytometry data is analyzed with Flowjo v8 software, Treestar, Inc., Ashlant, Oreg.). Group mean and standard deviation are determined for the control and treatment groups and data are graphed and analyzed using 1-way ANOVA with Tukey post test (Graphpad Prism v5, La Jolla, Calif.).
It is anticipated that the disclosed compounds and formulations will show improved fetal hemoglobin inducer effect on erythroid progenitor cells in vitro in the foregoing sickle cell assay compared to conventional compounds or formulations.
The following assays and model systems, e.g., tissue culture and/or in vivo models, can be used to assess safety and efficacy of the disclosed compounds and formulations as fetal hemoglobin inducer which are anticipated to provide improved outcomes in these assays compared to conventional compounds or formulations.
K562 cells are cultured in Iscove's Modified Dulbecco medium (IMDM) with 10% fetal bovine serum, penicillin (100 U/mL) and streptomycin (0.1 mg/mL). Drug inductions for K562 cells are conducted for 48 h and cell viability evaluated with 0.4% Trypan blue exclusion. Cell counts are performed a dual chamber apparatus and the percentage viability obtained using an Automated Cell Counter (Bio-Rad).
For primary cultures, erythroid precursors are generated from peripheral blood mononuclear cells isolated from discard blood of sickle cell patients under an IRB-exempt protocol. These cells are cultured in a two-phase liquid culture system that has been previously published. During phase 1, cells are grown in Iscove's Dulecco Media with 15% fetal bovine serum, 15% human AB serum, 10 ng/mL interleukin-3, 50 ng/mL stem cell factor, and 2 IU/mL of erythropoietin (Peprotech, Rocky Hill N.J.). Phase 2 of culture initiated on day 7 with a similar medium without stem cell factor or interleukin-3. On day 8, erythroid precursors are treated with AN-233 (0.125 mM and 0.25 mM), ethanol (EtOH; 0.0008% and 0.016%) and the positive control HU (100 μM) for 48 h and harvested for the various analyses.
Total RNA is extracted from cells using Trizol (Ambion, Carlsbad Calif.) and analyzed by RT-qPCR using a previously published procedure. Gene-specific primers are used to quantify mRNA levels for γ-globin, β-globin, and an internal control of glyceraldehyde-3-phosphate de-hydrogenase (GAPDH). All mRNA levels are normalized to GAPDH before analysis.
Western blot analysis is performed according to a previously published procedure using whole cell lysates generated with RIPA buffer (ThermoScientific, Rockford, Ill.) supplemented with proteinase and phosphatase inhibitor cocktails. For histone acetylation studies, nuclear lysates are prepared by suspending cells in buffer containing 20 mM HEPES, pH 7.9, 50 mM KCl, 420 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 10% glycerol and protease inhibitor mixture for 30 min, followed by centrifugation. Antibodies against HbF (51-7), HbA (37-8), and Tata binding protein (TBP; N-12) are purchased from Santa Cruz Biotechnology (Dallas Tex.); antibodies against β-actin (A5316) and rabbit IgG (18140) are purchased from Sigma (St. Louis Mo.). Acetylated histone H3 (AcH3; 06-599) and AcH4 (06-866) antibodies are purchased from Millipore (Burlington, Mass.).
To measure percent HbF positive cells (F-cells), K562 cells and erythroid precursors are fixed with 1% formaldehyde, permeabilized with ice-cold acetone:methanol (4:1 ratio), and stained with fluorescein isothiocyanate (FITC) anti-HbF antibody (ab19365, Abcam Cambridge Mass.), while isotype control IgG antibody (MBS524511, MyBioSource, San Diego Calif.) is used to detect non-specific staining. The F-cells levels and HbF protein levels measured by mean fluorescence intensity (MFI) are analyzed on an LSR-II flow cytometer (BD Biosciences, San Jose Calif.) and by FlowJo analysis to generate quantitative data.
The total cellular heme content is determined using the QuantiChrom™ Heme Assay Kit (DIHM-250, BioAssay Systems, Hayward, Calif.) per the manufacturer's instructions. Briefly, 25 μL of cellular lysate is mixed with 100 μL of detection reagent. The mixture is incubated at room temperature for 5 min followed by measuring the absorbance at 400 nm on a microplate reader. The total heme concentration is calculated based on a formula provided by the manufacturer: Heme concentration=(ODsample−ODblank)/(ODcalibrator−ODblank)×125×dilution factor. This value is normalized by total protein in each sample.
In vitro sickling studies are conducted according to a previously published procedure. Briefly, after drug inductions of sickle erythroid precursors for 48 h, cells are incubated in 2% oxygen overnight and then fixed with 2% formaldehyde. Erythroid morphology is evaluated microscopically and the number of sickled cells per high power field manually counted for 1000 cells, per triplicates per condition.
The β-YAC is a transgenic mouse model containing the full-length 81 kb human β-globin gene locus including the LCR and surrounding region. The five functional human globin genes 5′-ε-Gγ-Aγ-δ-β-3′ are present and undergo normal developmental regulation with the γ-globin gene silenced shortly after birth. β-YAC mice (5-6 months old) are administered AN-233 suspended in water (200 or 300 mg/kg) 5 days/week for 4 weeks by intraperitoneal injection; we treated five mice per group with 3 males and 2 females. Hydroxyurea (100 mg/kg) is included as a positive control. We collected blood by tail bleed at week 0, 2 and 4 and analyzed for automated complete blood counts with differential using a Micros 60 machine (HORIBA Medical/ABX Diagnostics). The level of F-cells and MFI are performed by flow cytometry as previously described. For reticulocyte counts, whole blood is stained with acridine orange and flow cytometry performed on an LSR-II flow cytometer (BD Biosciences).
Cell lysates are run on SDS-PAGE as previously described (Berkovitch et al., 2008). Following blocking, the membranes are incubated with rabbit anti-hemoglobin (Dako, Glostrup, Denmark), rabbit anti-PBGD (a generous gift from HemeBiotech, Sweden). The membranes are ished with PBS-Tween and incubated with horseradish peroxidase (HRP)-tagged anti-mouse secondary anti-body (Jackson ImmunoResearch Labs Inc., West Grove, Pa., USA) in the same solution used for blocking. The ratio of the protein level is normalized to HRP-conjugated mouse anti-β-actin (Santa Cruz Biotechnology, Santa Cruz, Calif., USA). Immunoreactive proteins are visualized with the EZ-ECL-enhanced chemiluminescence detection kit according to the manufacturer's protocol (Biological Industries).
For hemoglobin determination, the cells are grown in the presence of inducing agents, pelleted by low speed centrifugation, and ished twice with PBS. The ished cell pellets are then resuspended in an equal volume of distilled water. Cells are lysed by 3 cycles of freeze-thawing and centrifuged once at 2000 rpm for 10 min and again at 15,000 rpm for 45 min. The visible absorbance spectrum of the supernatant is recorded from 417 nm to 700 nm using a Epoch™ Microplate Spectrophotometer (Bio-Tek, US). Relative hemoglobin concentration of 5×17 cell lysates is measured at 540 nm.
Following treatments, 500 μg of cell lysate are added to 100 μL ortho-toluidine reagent, 0.25 g ortho-toluidine (Sigma-Aldrich, Rehovot, Israel) and dissolved in 80 mL glacial acetic acid and 10 mL dd H2O. After mixing, dd H2O is added to a final volume of 100 mL. Heme is oxidized to a green product by adding 100 μL of 1.2% H2O2 to the mixture and incubating for 10 min in the dark. The first oxidation product is then further oxidized to a yellow product by adding 1 mL of a 1:10 v/v diluted acetic acid.
ANTI-SOLVENT ADDITION. The anti-solvent crystallization experiments were performed by combining 10 different solvents with 10 anti-solvents. The anti-solvent crystallization experiments were performed by reverse addition in which a small amount of a near saturated solution of the aza-T-dCyd in the selected solvent was added to 20 mL of anti-solvent, which was vigorously agitated. The samples in which no precipitation occurred were placed at 5° C. for 3 days to induce precipitation. The precipitated solids were isolated from the mother liquor and analyzed by HT-XRPD after drying in a glovebox (20% RH) overnight and after drying under vacuum (10 mbar) overnight. All solids were exposed to accelerated aging conditions (2 days at 25° C./60% RH) and re-analyzed by HT-XRPD.
EVAPORATIVE CRYSTALLIZATION. For the evaporative crystallization experiments from solvent mixtures, new solutions were prepared from the crystalline starting material. The solutions were transferred to vials (without caps) and left in glovebox conditions (20% RH/RT) to allow the solvents to evaporate slowly for 3 days, followed by vacuum (10 mbar) at RT until all solvent was evaporated. The samples with NMP (Exp. ID ECP43 and ECP44) were further dried under vacuum at 50° C. The obtained solids were analyzed by HT-XRPD. Subsequently, the solids were placed at 25° C./60% RH for two days (AAC) and re-analyzed by XRPD.
SOLVENT EQUILIBRATION. The solvent equilibration experiments were performed in 29 solvents. To about 20 mg of aza-T-dCyd, the solvents were added in small steps until a thin suspension was obtained. The suspensions were left to equilibrate with continuous stirring for 5 days at 5° C. and 1 day at 25° C. After the equilibration time (1 day at RT and 5 days at 5° C.), the solids were separated by centrifugation. A part of the solids was collected and harvested on a 96 well plate and dried in a glovebox (with relative humidity of 20% at RT) overnight. The remaining solids were dried under vacuum (RT and 10 mbar) overnight and then harvested on a 96 well plate. All solids were analyzed by HT-XRPD. Subsequently, all solids were exposed to accelerated aging conditions for two days (AAC, 25° C./60% RH) and re-analyzed by HT-XRPD.
SONICATION. The sonication experiments were started with the crystalline aza-T-dCyd. About 20 mg of API was weighed in 1.8 mL vials and 5-10 μL of solvent was added until a paste was obtained. The pastes were sonicated at RT for 10 minutes in an ultrasonic bath (Fisher Scientific, FB15051). The solids were harvested and analyzed by HT-XRPD and re-analyzed after drying under vacuum (10 mbar/RT overnight). Subsequently, all the solids were exposed to accelerated aging conditions (25° C./60% RH) for two days and re-analyzed by HT-XRPD.
THERMOCYCLING CRYSTALLIZATION. The thermocycling crystallization experiments were performed in 20 organic solvents and solvent mixtures. To about 25 mg of aza-T-dCyd small aliquots of solvent (mixture) was added until a thin suspension was obtained at room temperature. Subsequently, the mixtures were placed in the Crystal16™ reactors to undergo a temperature profile as displayed in
After the temperature profile the solids were separated from the solution by centrifugation, a part was dried in a glovebox (20% RH) at RT and a part was dried under deep vacuum (10 mbar) before being harvested and analyzed by HT-XRPD. The liquid phases were also evaporated and recovered solids were analyzed by HT-XRPD. All solids were then exposed to accelerated aging conditions (2 days at 25° C./60% RH) followed by HT-XRPD re-analysis.
VAPOR DIFFUSION. The vapor diffusion into solution experiments were performed at RT. Near saturated solutions of the aza-T-dCyd were prepared in the solvents in 1.8 mL glass vials or 40 mL vials. The open vials containing the saturated solution were placed in a closed bigger vial containing 2-5 mL of anti-solvent. The samples were checked for solid formation after one week. The solids were analyzed by HT-XRPD after drying in a glovebox (20% RH) and after drying under vacuum (10 mbar). If no precipitation occurred, the solvent was evaporated under vacuum and the resulting solids analyzed by HT-XRPD. Subsequently, all solids were exposed to accelerated aging conditions (2 days at 25° C./60% RH) and re-analyzed by HT-XRPD.
HT-XRPD. XRPD patterns were obtained using the Ardena SSR T2 high-throughput XRPD set-up. The plates were mounted on a Bruker General Area Detector Diffraction System (GADDS) equipped with a VANTEC-500 gas area detector corrected for intensity and geometric variations. The calibration of the measurement accuracy (peaks position) was performed using NIST SRM1976 standard (Corundum). Data collection was carried out at room temperature using monochromatic CuKα radiation in the 2 Å region between 1.5° and 41.5°, which is the most distinctive part of the XRPD pattern. The diffraction pattern of each well was collected in two 20 ranges (1.5°≤2θ≤21.5° for the first frame, and 19.5°≤2θ≤41.5° for the second) with an exposure time of 90 s for each frame. No background subtraction or curve smoothing was applied to the XRPD patterns. The carrier material used during XRPD analysis was transparent to X-rays and contributed only slightly to the background.
HR-XRPD. The HR-XRPD data were collected on D8 Advance diffractometer using Cu Kα1 radiation (1.54056 Å) with germanium monochromator at RT. Diffraction data were collected in the 2θ range 2-41.5° 2θ. Detector scan on solid state LynxEye detector was performed using 0.016° per step with 5 sec/step scan speed. The samples were measured in 8 mm long glass capillary with 0.5 mm outer diameter.
TGMS ANALYSIS. Mass loss due to solvent or water loss from the crystals was determined by TGA. Monitoring the sample weight, during heating in a TGA/DSC 3+ STARe system (Mettler-Toledo GmbH, Switzerland), resulted in a weight vs. temperature curve and a heat flow thermogram. The TGA/DSC 3+ was calibrated for temperature with indium and aluminum. Samples (circa 2 mg) were weighed into 100 μL aluminum crucibles and sealed. The seals were pin-holed, and the crucibles heated in the TGA from 25 to 300° C. at a heating rate of 10° C./min. Dry N2 gas was used for purging. The gases evolved from the TGA samples were analyzed by an Omnistar GSD 301 T2 mass spectrometer (Pfeiffer Vacuum GmbH, Germany). This MS is a quadrupole mass spectrometer, which analyses masses in the range of 0-200 amu.
DSC ANALYSIS. Thermal events (i.e., melting, re-crystallization) were obtained from DSC thermograms, recorded with a heat flux DSC3+ STARe system (Mettler-Toledo GmbH, Switzerland). The DSC3+ was calibrated for temperature and enthalpy with a small piece of indium (m.p.=156.6° C.; δHf=28.45 J/g) and zinc (m.p.=419.6° C.; δHf=107.5 J/g). Samples (circa 2 mg) were sealed in standard 40 μL aluminum pans, pin-holed and heated in the DSC from 25° C. to 300° C., at a heating rate of 10° C./min. Dry N2 gas, at a flow rate of 50 mL/min was used to purge the DSC equipment during measurement. The cycling DSC experiments were measured in standard 40 μL aluminum pans, pin-holed and heated in the DSC from 25° C. to variable temperatures, then cooled back to 25° C. The heating and cooling rate was 10° C./min. Dry N2 gas, at a flow rate of 50 mL/min was used to purge the DSC equipment during measurement. Afterwards the samples were recovered and analyzed by HT-XRPD.
LCMS. LCMS experiments were performed on an Agilent 1290 series machine with diode array UV detector and MSD XT single quad mass detector. Mobile phases A and B are 10 mM ammonium acetate in water and acetonitrile, respectively. The column was a Waters XBridge HILIC (150×4.6 mm; 3.5 μm, pn. 186004441). Detection was at 244 nm, with a bandwidth of 4 nm, a UV spectrum of 200-400 nm. Spectrometry was performed in positive scan mode 100-800 m/z, 500 ms scan time. The flow rate was 0.8 mL/min. The run time was 10 minutes. Injection volume was 5 μL at 40° C., with an autosampler temperature of 8° C.
Form A obtained from the solvent equilibration experiment at RT in TFE was used for the analytical characterization. The TGMS result showed the release of about 0.7% of residual solvent in the temperature range 30-190° C. (
Form F obtained from the evaporative crystallization experiment using DMF/acetonitrile (80/20, v/v) was used for characterization. The TGMS result showed a small loss of 1.1% between 30 and 140° C., most likely due to residual solvent (
Form A had a higher melting temperature than Form F and can be considered as the thermodynamically more stable form. Both Form A and Form F are anhydrous.
It should be emphasized that the above-described embodiments of the present disclosure are merely possible examples of implementations set forth for a clear understanding of the principles of the disclosure. Many variations and modifications may be made to the above-described embodiment(s) without departing substantially from the spirit and principles of the disclosure. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims.
This application claims the benefit of U.S. Provisional Application No. 63/256,428, filed Oct. 15, 2021, and is incorporated by reference herein.
| Number | Date | Country | |
|---|---|---|---|
| 63256428 | Oct 2021 | US |
