Patent Application
20180250354
The invention relates to compositions and methods for long term release of Gonadotropin-releasing hormone (GnRH) antagonists and uses thereof. Specifically, the invention relates to polymer-based compositions and methods for controlled release of GnRH antagonists.
The hypothalamic hormone, gonadotropin-releasing hormone (GnRH) (also known as luteinizing hormone releasing hormone (LHRH)), controls the secretion of the gonadotropins, luteinizing hormone (LH) and follicle stimulating hormone (FSH) from the anterior pituitary gland. Analogues of GnRH are currently used to treat many medical conditions that require manipulation of the production of the sex hormones, testosterone and estrogen. Schally et al. (Schally 1971) isolated, identified the amino acid sequence, and synthesized the peptide hormone GnRH. Deletion or replacement of different amino acids of GnRH peptide has resulted in the discovery of distinct GnRH agonist analogues that demonstrate greater relative potency for the secretion of LH and FSH. A paradoxical clinical effect occurs when agonistic analogues are used continuously such that after the chronic, and relatively long period (2-3 weeks) of stimulation of the secretion of LH and FSH, there is actually an inhibition of LH and/or FSH release and consequent suppression of sex steroid production (testosterone and estrogen). (Reissmann 2000). In certain medical conditions, however, an immediate and dose-dependent suppression of LH and FSH is desired. Over 20 years ago, Schally and Revier synthesized the 1dt generation analogues of GnRH antagonist analogues which were too lipophilic and induced histamine release. (Schmidt 1984; Hahn 1985). The 2nd generation GnRH antagonist analogues were made by incorporating further amino acid substitutions (Bajusz 1988; Rivier 1993) that resulted in potentially safer and more effective decapeptide analogues. Examples of newer generation GnRH antagonist analogues include degarelix, ganirelix, ozarelix, cetrorelix, taverelix, antarelix, and iturelix.
Clinical development and medical applications of these GnRH antagonist analogues have been either successful or attempted for controlled ovarian stimulation for assisted reproductive techniques, uterine myoma, ovarian cancer, benign prostatic hyperplasia, and prostate cancer. In certain diseases and conditions, the major limitation for successful application of the GnRH antagonist analogue has been having only a short acting formulation where longer acting depot formulations would be more clinically advantageous for optimal drug compliance.
Accordingly, there exists a need for very long acting controlled or extended release formulations of a GnRH antagonist (also called a LHRH antagonist).
In an embodiment, the invention relates to a long-term drug release composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a polymer, wherein said composition is capable of releasing said GnRH antagonist for a duration of at least four months.
In another embodiment, the invention relates to a flowable composition, the composition comprising: (a) a biodegradable thermoplastic polyester that is substantially insoluble in aqueous medium or body fluid; (b) a biocompatible polar aprotic solvent, wherein the biocompatible polar aprotic solvent is miscible to dispersible in aqueous medium or body fluid; and (c) a therapeutically effective amount of a GnRH antagonist, wherein said flowable composition is capable of releasing said GnRH antagonist for a duration of at least four months. In exemplary embodiments of the compositions, the GnRH antagonist is cetrorelix, degarelix, ganirelix, ozarelix, taverelix, antarelix, or iturelix. In various embodiments, said polymer is poly(glycolide) (PLG), poly (lactide) (PLA), or poly-lactic co-glycolic acid (PLGA).
In some embodiments, the invention relates to a composition for a long-term release of cetrorelix, the composition comprising a biodegradable polymer, a solvent, and a therapeutically effective amount of cetrorelix, wherein the release duration is at least four months.
In various embodiments, the invention relates to a method for extending the release of cetrorelix in a subject for a duration of at least four months, the method comprising administering to said subject a composition comprising cetrorelix and a polymer, wherein said polymer comprises poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio between 50:50 and 100:0, wherein cetrorelix is present in an amount of 5%-90% of the mass of said composition, and said polymer is present in an amount of 10%-50% of the mass of said composition.
In other embodiments, the invention relates to a method for maintaining a therapeutic level of cetrorelix in a subject for a duration of at least four months, the method comprising administering to said subject a composition comprising cetrorelix and a polymer, said polymer comprising poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio between 50:50 and 100:0, wherein cetrorelix is present in an amount of 5%-90% of the mass of said implant, and said polymer is present in an amount of 10%-50% of the mass of said implant.
In certain embodiments, the invention relates to a composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a multi-block copolymer, wherein said polymer comprises polyethyleneglycol(PEG)-PLGA-PEG, poly(3-hydroxybutyrate), PCL, PLG, PLA, or a combination thereof, wherein said composition is capable of achieving a therapeutic effect within 24 hours and maintains therapeutic effect for at least 133 days.
In various embodiments, the invention relates to a composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a multi-block copolymer, wherein said multi-block copolymer comprises randomly or non-alternatingly arranged hydrolysable segments, wherein each segment comprises pre-polymer A or pre-polymer B, and wherein said segments are operably linked to each other by a multifunctional chain extender, wherein said composition is capable of achieving a therapeutic effect within 24 hours and maintains therapeutic effect for at least 133 days.
In some embodiments, the invention relates to a method for treating a disease or condition associated with gonadotropin-releasing hormone (GnRH), the method comprising administering to a subject a composition of any of the above claims, thereby treating said disease in said subject, wherein said composition is capable of achieving a therapeutic effect within 24 hours and maintains therapeutic effect for at least 133 days.
In various embodiments, the invention relates to a composition comprising cetrorelix and a polymer, said polymer comprising poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio between 50:50 and 100:0, wherein cetrorelix is present in an amount of 5%-90% of the mass of said composition, and said polymer is present in an amount of 10%-50% of the mass of said composition, and wherein said composition is capable of extending the release of cetrorelix in a subject for a duration of at least four months. In other embodiments, the composition comprises cetrorelix and a polymer, said polymer comprising poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio of 75:25. In certain embodiments, the composition comprises cetrorelix and a polymer, said polymer comprising poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio of 85:15.
In one aspect, the invention relates to a composition, said composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a polymer, wherein said polymer is poly(glycolide) (PLG), poly(lactide) (PLA), or poly-lactic co-glycolic acid (PLGA), wherein said composition is capable of releasing said GnRH antagonist for a long term (e.g., more than 90 days, or more than 119 days). In an exemplary embodiment, GnRH antagonist is cetrorelix, degarelix, ganirelix, ozarelix, taverelix, antarelix, or iturelix.
In another aspect, the invention relates to a composition, said composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a non-PLGA block polymer, wherein said polymer is polyethyleneglycol (PEG), PLG, PLA, polybutylene terephthalate (PBT), poly(epsilon-caprolactone) (PCL), dioxanone, butanediisocyanate, butanediol, polyoxyethylene, polypropylene, polyoxypropylene, polystyrene, poly methyl methacylate, or a combination thereof, wherein said composition is capable of releasing said GnRH antagonist for a long term.
In another aspect, the invention relates to a flowable composition, the composition comprising: (a) a biodegradable thermoplastic polyester that is at least substantially insoluble in aqueous medium or body fluid; (b) a biocompatible polar aprotic solvent, wherein the biocompatible polar aprotic solvent is miscible to dispersible in aqueous medium or body fluid; and (c) a therapeutically effective amount of a GnRH antagonist. In an exemplary embodiment, the thermoplastic polyester is a polylactide, a polyglycolide, a polycaprolactone, a copolymer thereof, a terpolymer thereof, or any combination thereof. In another exemplary embodiment, the solvent is N-methyl-2-pyrrolidone, 2-pyrrolidone, N,N-dimethylformamide, dimethyl sulfoxide, propylene carbonate, caprolactam, triacetin, or any combination thereof. In a particular embodiment, the flowable composition of the invention comprises a flowable delivery system such as an Atrigel® system comprising a copolymer, a water soluble organic solvent, and a bioactive agent, for example, a GnRH antagonist.
In another aspect, the invention relates to a composition, said composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a multi-block copolymer, wherein said polymer comprises polyethyleneglycol(PEG)-PLGA-PEG, poly(3-hydroxybutyrate), PCL, PLG, PLA, or a combination thereof.
In another aspect, the invention relates to a composition, said composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a multi-block copolymer, wherein said multi-block copolymer comprises randomly or non-alternatingly arranged hydrolysable segments, wherein each segment comprises pre-polymer A or pre-polymer B, and wherein said segments are operably linked to each other by a multifunctional chain extender. In an exemplary embodiment, said multi-block copolymer is a phase separated multiblock copolymer, comprising: one or more segments of a linear soft biodegradable pre-polymer A having a glass transition temperature (Tg) lower than 37° C.; and one or more segments of a linear hard biodegradable pre-polymer B having a melting point temperature (Tm) of 40-100° C.
In another aspect, the invention relates to the use of salt bridges or cyclization of the active agent either as a primary drug delivery technique or in combination with another drug delivery vehicle using compounds that include, but are not limited to, lanthionine, dicarba, hydrazine, or lactam bridges.
In another aspect, the invention relates to the use of micronization or stabilizing adjuvants for a long-term delivery of a GnRH antagonist.
In another aspect, the invention relates to the use of a solid-in-oil-in-water (S/O/W), a water-in-oil-in water (W/O/W), or a water-oil (W/O) production method for long term delivery of a GnRH antagonist.
In an exemplary embodiment, the composition is capable of achieving a therapeutic effect within, for example, 24 hrs and maintains therapeutic effect for at least 90 days (or for more than 119 days) for >95% percent of treated patients. In a particular embodiment, the composition is in the form of a hydrogel. In another particular embodiment, the composition is in the form of microspheres.
The composition of the invention can be administered using a suitable method. In one aspect, the composition of the invention is an injectable composition, which is administered with one injection or two injections administered at the same time using, for example, a 21 gauge needle or smaller, with a total injection volume, for example, less than 4 mL. Injections may be subcutaneous or intramuscular.
In another aspect, the invention relates to a method for extending the release of a GnRH antagonist (e.g., cetrorelix) in a subject for a period ranging from about 1 month to about 6 months, the method comprising administering to said subject a composition comprising cetrorelix and a polymer, said polymer comprising poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio between 50:50 and 100:0, wherein cetrorelix is present in an amount of 5%-90% of the mass of said composition, and said polymer is present in an amount of 10%-50% of the mass of said composition.
In another aspect, the invention relates to a method of maintaining a therapeutic level of a GnRH antagonist (e.g., cetrorelix) in a subject for a period ranging from about 1 month to about 6 months, the method comprising administering to said subject a composition comprising cetrorelix and a polymer, said polymer comprising poly-lactic co-glycolic acid (PLGA) in a lactide:glycolide molar ratio between 50:50 and 100:0, wherein cetrorelix is present in an amount of 5%-90% of the mass of said composition, and said polymer is present in an amount of 10%-50% of the mass of said composition.
In another aspect, the composition of the invention allows for consistent release of the active agent from the drug delivery vehicle with no more than 25% variation plus an encapsulation efficiency of over 70%. In yet another aspect, the composition of the invention allows Releases the active agent from the drug delivery vehicle with >85% intact over the entire duration of release.
Other features and advantages of the present invention will become apparent from the following detailed description examples and figures. It should be understood, however, that the detailed description and the specific examples while indicating preferred embodiments of the invention are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.
The present subject matter may be understood more readily by reference to the following detailed description which forms a part of this disclosure. It is to be understood that this invention is not limited to the specific products, methods, conditions or parameters described and/or shown herein, and that the terminology used herein is for the purpose of describing particular embodiments by way of example only and is not intended to be limiting of the claimed invention.
Unless otherwise defined herein, scientific and technical terms used in connection with the present application shall have the meanings that are commonly understood by those of ordinary skill in the art. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular.
As employed above and throughout the disclosure, the following terms and abbreviations, unless otherwise indicated, shall be understood to have the following meanings.
In the present disclosure the singular forms “a,” “an,” and “the” include the plural reference, and reference to a particular numerical value includes at least that particular value, unless the context clearly indicates otherwise. Thus, for example, a reference to “a compound” is a reference to one or more of such compounds and equivalents thereof known to those skilled in the art, and so forth. The term “plurality”, as used herein, means more than one. When a range of values is expressed, another embodiment incudes from the one particular and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it is understood that the particular value forms another embodiment. All ranges are inclusive and combinable.
The invention relates to a controlled release composition comprising a gonadotropin-releasing hormone (GnRH) antagonist in combination with one or more polymers and/or salts.
The composition may include any suitable a GnRH antagonist, known to one of skilled in the art. GnRH is also known as follicle-stimulating hormone-releasing hormone (FSH-RH), luteinizing hormone-releasing hormone (LHRH), gonadoliberin, and by various other names, known to one of skilled in the art.
In a particular embodiment, the GnRH antagonist is cetrorelix, abarelix, degarelix, ganirelix, ozarelix, taverelix, antarelix, or iturelix.
In one aspect, provided herein is a composition, said composition comprising a therapeutically effective amount of a GnRH antagonist in combination with a polymer, wherein said polymer is poly(glycolide) (PLG), poly(lactide) (PLA), or poly-lactic co-glycolic acid (PLGA), wherein said composition is capable of releasing said GnRH antagonist for a long term (e.g., at least four months). In a particular embodiment, the composition is capable of releasing said GnRH antagonist for at least 119 days. In certain embodiments, the composition releases said GnRH antagonist (e.g., cetrorelix) for at least 119 days. In some embodiments, the composition is capable of achieving a therapeutic effect within 24 hours and maintains therapeutic effect for at least 133 days. In certain embodiments, the composition achieves a therapeutic effect within 24 hours and maintains the therapeutic effect for at least 133 days.
In particular embodiments, the invention relates to a composition for a long-term release of cetrorelix, the composition comprising a biodegradable polymer, a solvent, and a therapeutically effective amount of cetrorelix, wherein the long-term release is a duration of at least four months.
In another aspect, provided herein is a composition, said composition comprising: a therapeutically effective amount of a GnRH antagonist in combination with a non-PLGA block polymer, wherein said composition is capable of releasing said GnRH antagonist for a long term. Non-PLGA polymers are well known in the art. Examples of a non-PLGA block polymer include, for example, but are not limited to, polyethyleneglycol (PEG), PLG, PLA, polybutylene terephthalate (PBT), poly(epsilon-caprolactone) (PCL), dioxanone, butanediisocyanate, butanediol polyoxyetylene, polypropylene, polyoxypropylene, polystyrene, poly methyl methacylate, or a block copolymer which additionally incorporates one more novel amphiphilic, hydrophilic, or hydrophobic component. In another aspect, a non-PLGA block polymer comprises a blend of two or more polymer types capable of releasing therapeutically effective amount of GnRH antagonists.
In one aspect, the composition is a flowable composition capable of forming an in situ implant in a subject. In one example, the composition includes a biodegradable thermoplastic polymer, a biocompatible solvent; and a GnRH antagonist.
In another aspect, the invention relates to a flowable composition, the composition comprising: (a) a biodegradable thermoplastic polyester that is at least substantially insoluble in aqueous medium or body fluid; (b) a biocompatible polar aprotic solvent, wherein the biocompatible polar aprotic solvent is miscible to dispersible in aqueous medium or body fluid; and (c) a therapeutically effective amount of cetrorelix.
The biodegradable thermoplastic polymer can be substantially insoluble in aqueous medium or body fluid. Biodegradable thermoplastic polymers are well known in the art and fully described in U.S. Pat. Nos. 6,565,874; 5,324,519; 4,938,763; 5,702,716; 5,744,153; and 5,990,194, which are incorporated by reference herein in their entirety. In one embodiment, biodegradable thermoplastic polymer is a polyester, for example, including but not limited to, a polylactide, a polyglycolide, a polycaprolactone, a copolymer thereof, a terpolymer thereof, or any combination thereof.
The type, amount, and molecular weight, of biodegradable thermoplastic polymer present in the composition may depend upon one or more desired properties of the controlled release implant.
Examples of types of biodegradable thermoplastic polyesters are well known in the art and fully described in U.S. Pat. No. 6,565,874, which is incorporated by reference herein in its entirety. In a particular embodiment, the suitable biodegradable thermoplastic polyester is 50:50 poly (DL-lactide-co-glycolide) having a carboxy terminal group or is 75:25 poly (DL-lactide-co-glycolide) with a carboxy terminal group that is protected. Other suitable copolymers, known to one of skilled in the art, can also be used.
In another aspect, the PLGA polymers in the compositions of the present invention may have lactide:glycolide weight ratio ranging from about 50:50 to about 100:0. In particular embodiments, the lactide to glycolide ratio is about, 50:50, 55:45, 60:40, 65:35, 70:30, 75:25, 80:20, 85:15, 90:10, or 95:5.
The PLGA polymers the compositions of the present invention may comprise a mixture of two or more PLGA polymers each having a different glycolide and lactide fractions. For example, the mixture may include a first PLGA polymer having equal amount of glycolide and lactide (RG502H) and a second PLGA polymer having 25% glycolide and 75% lactide (RG752H). The proportions of the first PLGA polymer and the second PLGA polymer may vary, for example the ratio of RG502H to RG752H can range from about 100:0 to about 0:100.
The amount of biodegradable thermoplastic polymer, in the composition, can be any suitable amount, known to one of skilled in the art. The amount, in the composition, may range from about 10 wt. % to about 80 wt. %; from about 20 wt. % to about 60 wt. %; from about 25 wt. % to about 55 wt. %; from about 30 wt. % to about 50 wt. %; or from about 35 wt. % to about 45 wt. %. In a particular embodiment, the amount is approximately 10, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, or 80 wt. %.
The molecular weight of biodegradable thermoplastic polymer, in the composition, can be any suitable molecular weight, known to one of skilled in the art. The molecular weight may range from about 10,000 to about 50,000; from about 15,000 to about 45,000; from about 20,000 to about 40,000; or from about 20,000 to about 30,000. In a particular embodiment, the molecular weight is approximately 10,000, 15,000, 20,000, 25,000, 30,000, 35,000, 40,000, 45,000, or 50,000.
In particular embodiments, the biodegradable thermoplastic polyester has an average molecular weight ranging from about 23,000 to about 45,000 or from about 15,000 to about 24,000.
The biocompatible solvent can be a biocompatible polar aprotic solvent. In one embodiment, the solvent is miscible to dispersible in aqueous medium or body fluid. Suitable polar aprotic solvents are well known in the art and fully described in, for example, in Aldrich
Handbook of Fine Chemicals and Laboratory Equipment, Milwaukee, Wis. (2000) and U.S. Pat. Nos. 6,565,875, 5,324,519; 4,938,763; 5,702,716; 5,744,153; and 5,990,194, which are incorporated by reference herein in their entirety.
In one aspect, the solvent of the invention is capable of diffusing into body fluid so that the flowable composition coagulates or solidifies. In another aspect, the solvent of the invention is biodegradable. In yet another aspect, the solvent of the invention is non-toxic. As set forth in U.S. Pat. No. 6,565,875, examples of suitable polar aprotic solvents include polar aprotic solvents having an amide group, an ester group, a carbonate group, a ketone, an ether, a sulfonyl group, or a combination thereof.
In one embodiment, the polar aprotic solvent is N-methyl-2-pyrrolidone, 2-pyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, propylene carbonate, caprolactam, triacetin, or any combination thereof. In another embodiment, the polar aprotic solvent is N-methyl-2-pyrrolidone.
As set forth in U.S. Pat. No. 6,565,875, the polar aprotic solvent can be present in any suitable amount. The type and amount of biocompatible polar aprotic solvent present in the composition may depend upon the desired properties of the controlled release implant.
In a particular embodiment, the type and amount of biocompatible polar aprotic solvent can influence the length of time in which the GnRH antagonist is released from the controlled release implant.
In various embodiments of the long-term release GnRH antagonist composition (e.g., cetrorelix), the solvent may be present at the concentration ranging from about 10% to about 30% (w/w). For example, the cetrorelix may be present at a concentration ranging from about 5% to about 90% (w/w).
In certain embodiments, the composition may further comprise a salt, i.e., a salt of the GnRH antagonist (e.g., cetrorelix). Examples of a salt, include but are not limited to calcium pamoate (Ca pamoate), sodium pamoate (Na pamoate) and calcium citrate (Ca citrate).
In another aspect, the invention relates to a method of preparing a flowable composition, the method comprising: mixing a biodegradable thermoplastic polymer, a biocompatible solvent; and a GnRH antagonist. The mixing may be performed for a sufficient period of time effective to form the flowable composition for use as a controlled release implant.
In yet another aspect, the invention relates to an implant formed in situ by the process of injecting the composition of the invention to a subject; allowing the solvent, in said composition, to dissipate to produce a solid biodegradable implant.
In yet another aspect, the invention relates to a method of forming an implant in situ in a subject, the method comprising the steps of: injecting the composition of the invention to a subject; allowing the solvent, in said composition, to dissipate to produce a solid biodegradable implant.
In one example, the flowable composition of the invention comprises a flowable delivery system such as an Atrigel® system comprising a copolymer, a water soluble organic solvent, and a bioactive agent, for example, a GnRH antagonist.
The invention relates to a controlled release composition comprising a gonadotropin-releasing hormone (GnRH) antagonist (e.g., cetrorelix) loaded in a multi-block copolymer.
In one aspect, the inventor relates to a multi-block copolymer composition having a gonadotropin-releasing hormone (GnRH) antagonist (e.g., cetrorelix) as a bioactive agent. The multi-block copolymer compositions are well known and fully described in U.S. Pat. Nos. 8,481,651; 8,674,032; 8,674,033; and 9,364,442 and U.S. Patent Application Publications 2013/0209568; 2013/0273284; and 2014/0199385, and PCT International Patent Application Publications WO2005068533; WO2004007588; WO2012005594; and WO2013015685, all of which are incorporated by reference herein in their entirety.
The multi-block copolymer comprises one or more hydrolysable segments. In one embodiment, the multi-block copolymer comprises one or more randomly arranged hydrolysable segments. In another embodiment, the multi-block copolymer comprises one or more non-randomly arranged hydrolysable segments. In yet another embodiment, the multi-block copolymer comprises one or more alternatingly arranged hydrolysable segments. In yet another embodiment, the multi-block copolymer comprises one or more non-alternatingly arranged hydrolysable segments.
In some embodiments, the segments can be randomly and non-alternatingly connected to each other by multi-functional chain extenders.
In one example, the multi-block copolymer is amorphous at human body conditions.
In an exemplary embodiment, the multi-block copolymer has a glass transition temperature below body temperature at human body conditions.
In another aspect, the multi-block copolymer includes pre-polymer A, pre-polymer B, or a combination thereof. In one embodiment, pre-polymers A and B are composed of different monomers. In another embodiment, pre-polymers A and B are composed of the same monomers but in a different amount. In yet another embodiment, the pre-polymers are composed of the same monomers but with a different initiator in order to obtain the multi-block copolymers of the present invention.
Pre-polymers A and B are selected in such a way that the segments would exhibit significantly different properties, for example, but not limited to thermal, degradation and hydrophilic properties.
The pre-polymers A or B may comprise a hydrolysable polyester, poly ether ester, polycarbonate, polyester carbonate, polyanhydride or copolymers thereof, derived from cyclic monomers such as lactide (L, D or L/D), glycolide, ϵ-caprolactone, δ-valerolactone, trimethylene carbonate, tetramethylene carbonate, 1,5-dioxepane-2-one, 1,4-dioxane-2-one (para-dioxanone) or cyclic anhydrides (oxepane-2,7-dione).
In one embodiment, pre-polymer includes ester. In another embodiment, pre-polymer includes carbonate. In yet another embodiment, pre-polymer includes an anhydride linkage. In some embodiments, pre-polymer optionally comprises a polyether group. In an exemplary embodiment, polyether is present as an additional pre-polymer.
In one example, pre-polymer comprises a reaction product of an ester forming monomer selected from the group consisting of diols, dicarboxylic acids and hydroxycarboxylic acids.
In another example, pre-polymer comprises reaction products of at least one suitable cyclic monomer with at least one non-cyclic initiator selected from the group consisting of diols, dicarboxylic acids and hydroxycarboxylic acids.
Examples of cyclic monomer include, for example, but are not limited to, glycolide, lactide (L, D or DL), ϵ-caprolactone, δ-valerolactone, trimethylene carbonate, tetramethylene carbonate, 1,4-dioxane-2-one (para-dioxanone), 1,5-dioxepane-2-one and cyclic anhydrides.
In some embodiments, pre-polymer comprises at least two different cyclic monomers. In one example, pre-polymer comprises glycolide and E-caprolactone in a 1:1 weight ratio. In another example, pre-polymer comprises glycolide and lactide in a 1:1 weight ratio.
Examples of non-cyclic initiator include, for example, but are not limited to, succinic acid, glutaric acid, adipic acid, sebacic acid, lactic acid, glycolic acid, hydroxybutyric acid, ethylene glycol, diethylene glycol, 1,4-butanediol and 1,6-hexanediol.
Examples of polyether groups include, for example, but are not limited to, PEG (polyethylene glycol), PEG-PPG (polypropylene glycol), PTMG (polytetramethylene ether glycol) and combinations thereof. In a particular embodiment, the polyether group is PEG. PEG can be an initiator for ring-opening polymerization. PEG with any suitable molecular weight can be used, for example, a molecular weight between 150-4000. In one embodiment, each of pre-polymers A and B has a number average molecular weight between 300 and 30000.
In a particular embodiment, the composition comprises a polyethylene glycol (PEG). Any suitable PEG known to one of skilled in the art can be used. In an exemplary embodiment, PEG is polyethylene glycol 200, polyethylene glycol 300, or methoxy polyethylene glycol 350.
The chain-extender of the invention can be any suitable multifunctional chain extender, known to one of skilled in the art. In one embodiment, the pre-polymers are linked by the di-functional chain-extender. Examples of di-functional chain-extender include, for example, but are not limited to, a diisocyanate chain-extender, a diacid and a diol compound.
The amount of pre-polymer, in the composition, can be any suitable amount, known to one of skilled in the art. The amount, in the composition, may be of about10-90 wt. %.
The methods for synthesis of pre-polymers and multi-block copolymer compositions are well known and fully described in U.S. Pat. Nos. 8,481,651; 8,674,032; 8,674,033; and 9,364,442 and U.S. Patent Application Publications 2013/0209568; 2013/0273284; and 2014/0199385, and PCT International Patent Application Publications WO2005068533; WO2004007588; WO2012005594; and WO2013015685, all of which are incorporated by reference herein in their entirety.
The intrinsic viscosity also may vary depending on one or more desired properties. In some embodiment, the intrinsic viscosity is larger than about 0.1 dl/g and less than about 6 dl/g. In one embodiment, the intrinsic viscosity lies between about 0.2-4 dl/g, more preferably between 0.4-2 dl/g.
In another aspect, the invention relates to phase separated multi block copolymers. The term “phase-separated,” as used herein, may refer to a system, for example, a copolymer having two or more different pre-polymers, of which at least two are incompatible with each other at temperatures of 40° C. or below (when kept at body conditions). As a result, the pre-polymers do not form a homogeneous mixture when combined as a physical mixture or chemical mixture.
The phase separated multi block copolymers are well known in the art and fully described in U.S. Pat. Nos. 9,364,442 and 8,674,033, and PCT International Patent Application
Publications WO2012005594 and, WO2004007588 which are incorporated by reference herein in their entirety. The phase-separated quality of the copolymers of the present invention is reflected in the profile of the glass transition temperature (Tg), melting temperature (Tm), or a combination thereof. For example, the phase-separated copolymers are characterized by at least two-phase transitions, each of which is related to (but not necessarily identical to) the corresponding Tg or Tm values of the prepolymers which are comprised in the copolymer. In an exemplary embodiment, the multi-block copolymer is a phase separated multiblock copolymer, comprising: one or more segments of a pre-polymer A (e.g., a linear soft biodegradable pre-polymer A) having a glass transition temperature (Tg) lower than 37° C.; and one or more segments of a pre-polymer B (e.g., a linear hard biodegradable pre-polymer B) having a melting point temperature (Tm) ranging from about 40° C. to about 100° C.
In another aspect, the invention relates to a composition, said composition comprising: a therapeutically effective amount of a cetrorelix in combination with a multi-block copolymer, wherein said multi-block copolymer comprises randomly or non- alternatingly arranged hydrolysable segments, wherein each segment comprises pre-polymer A or pre-polymer B, and wherein said segments are operably linked to each other by a multifunctional chain extender. In an exemplary embodiment, said multi-block copolymer is a phase separated multiblock copolymer, comprising: one or more segments of a linear soft biodegradable pre-polymer A having a glass transition temperature (Tg) lower than 37° C.; and one or more segments of a linear hard biodegradable pre-polymer B having a melting point temperature (Tm) of 40-100° C.
The multi-block copolymer compositions may be in any suitable form, for example, in the form of implant, microspheres, microrods, microparticles, injectable gel formulation, coatings or membranes or devices, or any other form known in the art.
In another aspect, the invention relates to the use of salt bridges or cyclization of the active agent either as a primary drug delivery technique or in combination with another drug delivery vehicle using compounds that include, but are not limited to, lanthionine, dicarba, hydrazine, or lactam bridges. The formation of salt bridges for linking through non-covalent bonds are well known in the art and fully described in PCT patent application publications WO2009/155257 and WO 2012/163519, which are incorporated by reference herein in their entirety.
In another aspect, the invention relates to the use of micronization or stabilizing adjuvants for a long-term delivery of a GnRH antagonist. Micronization techniques are well known in the art and fully described, for example, in PCT international Patent Application Publication WO2011/034514 and U.S. Patent Application Publication US2014/0219954, all of which are incorporated by reference herein in their entirety. Stabilizing adjuvants are also well known in the art and fully described, for example, in U.S. Pat. No. 7,611,709, which is incorporated by reference herein in its entirety.
In another aspect, the invention relates to the use of a solid-in-oil-in-water (S/O/W), a water-in-oil-in water (W/O/W), or a water-oil (W/O) production method for long term delivery of a GnRH antagonist. These methods are well known in the art and fully described, for example, in PCT international Patent Application Publications WO2015/145353; WO2003/099262; and WO2007/129926 and U.S. Patent Application Publications US2002/0055461; US2008/0268004; and US2010/0019403, which are incorporated by reference herein in their entirety.
In an exemplary embodiment, the composition is capable of achieving a therapeutic effect, for example, within 24 hrs. and maintains therapeutic effect for at least 90 days in, for example, >95% percent of treated patients. In alternate embodiments, the composition is capable of achieving a therapeutic effect within 24 hrs. and maintains the therapeutic effect for at least 133 days in, for example, >95% percent of treated patients. In a particular embodiment, the composition is in the form of a hydrogel. In another particular embodiment, the composition is in the form of microspheres. In particular embodiments, the microspheres are loaded with a GnRH antagonist (e.g., cetrorelix) and a salt (i.e., a cetrorelix salt) or without salt. The salt may be Ca pamoate, Na pamoate and Ca citrate.
Microspheres for sustained release of therapeutically active agents and methods of their preparations are well known in the art (see e.g. U.S. Pat. Nos. 6,458,387 and 9,381,159 incorporated by reference herein in their entirety). The microspheres typically comprise a matrix formed of biodegradable polymer. In some embodiments, the inner matrix diffuses through the outer surface under appropriate conditions. In some embodiments, the outer surface not only allows aqueous fluids to enter the microsphere, but also allows solubilized drug and polymer to exit the microsphere. The microspheres can be made to release drug and polymer from the interior of the microsphere when placed in an appropriate aqueous medium, such as body fluids or a physiologically acceptable buffer under physiological conditions over a prolonged period of time, thereby providing sustained release of a drug. In one embodiment, the microspheres can be made to release a drug without an initial burst or rapid drug release.
The microspheres have a generally uniform size (substantially spherical) and shape, with each preparation having a narrow size distribution. Microspheres range in size from about 0.5 microns to about 100 microns, depending upon the fabrication conditions. The characteristics of the microspheres may be altered during preparation by manipulating the water-soluble polymer concentration, reaction temperature, pH, concentration of therapeutic agent, crosslinking agent, and/or the length of time the macromolecule is exposed to the crosslinking agent and/or the energy source. In one example, microspheres are suitable for oral or parenteral administration; mucosal administration; ophthalmic administration; intravenous, subcutaneous, intra articular, or intramuscular injection; administration by inhalation; or topical administration.
The amount of polymer matrix, in the microsphere composition, can be any suitable amount, known to one of skilled in the art. The amount, in the microsphere composition, may range from about 10 wt. % to about 50 wt. %; from about 20 wt. % to about 40 wt. %; from about 25 wt. % to about 35 wt. %. In a particular embodiment, the amount is approximately 10, 20, 25, 30, 35, 40, 45, or 50 wt. %.
The amount of therapeutic molecule in the microsphere can range from about 1 wt. % to about 90 wt. %, from about 1 wt. % to about 40 wt. %, from about 3 wt. % to about 30 wt. %, from about 5 wt. %. to about 20 wt. %, from about 10 wt. %. to about 15 wt. %. In a particular embodiment, the amount is approximately 1, 3, 5, 7, 9 10, 15 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, or 90 wt. %.
The composition of the invention can be administered using a suitable method. In one aspect, the composition of the invention is an injectable composition, which is administered with one injection or two injections administered at the same time using, for example, a 21 G needle or smaller, with a total injection volume, for example, less than 4 mL. Injections may be subcutaneous or intramuscular.
The invention also relates to a kit, wherein the kit comprising: the composition of the invention.
In another aspect, the composition of the invention allows for consistent release of the active agent from the drug delivery vehicle with no more than 25% variation plus an encapsulation efficiency of over 70%. In yet another aspect, the composition of the invention allows the releases the active agent from the drug delivery vehicle with >85% intact over the entire duration of release.
In a further aspect, the invention relates to a method of extending release of a pharmaceutical agent (e.g. cetrorelix) in a subject for a period ranging from about 1 month to about 6 months, the method comprising administering to said subject a composition of the invention (e.g. microspheres). In another aspect, the invention relates to a method of extending the release of a pharmaceutical agent (e.g. cetrorelix) in a subject for a period of at least 90 days, the method comprising administering to said subject a composition of the invention (e.g. microspheres).
In a yet further aspect, the invention relates to a method of maintaining an effective level of a therapeutic agent (e.g. cetrorelix) in a subject for a period ranging from about 1 month to about 6 months, the method comprising administering to said subject a composition of the invention (e.g. microspheres). In another aspect, the invention relates to a method of maintaining an effective level of a therapeutic agent (e.g. cetrorelix) in a subject for a period at least 90 days, the method comprising administering to said subject a composition of the invention (e.g. microspheres).
In yet another aspect, the invention relates to a method for treating a disease or condition associated with GnRH, the method comprising administering a therapeutically effective amount of the composition of the invention, thereby treating said disease in said subject.
Effective doses of the compositions of the present invention, for treatment of conditions or diseases as described herein vary depending upon many different factors, including means of administration, target site, physiological state of the patient, whether the patient is human or an animal, other medications administered, and whether treatment is prophylactic or therapeutic. Usually, the patient is a human, however non-human mammals, including transgenic mammals, can also be treated. Treatment dosages may be titrated using routine methods known to those of skill in the art to optimize safety and efficacy.
The pharmaceutical compositions of the invention may include a “therapeutically effective amount.” A “therapeutically effective amount” refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired therapeutic result. A therapeutically effective amount of a molecule may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the molecule to elicit a desired response in the individual. A therapeutically effective amount is also one in which any toxic or detrimental effects of the molecule are outweighed by the therapeutically beneficial effects.
The compositions of the invention described herein can be used to treat any GnRH associated disease or condition that could be treated by GnRH antagonist in humans or animals. Examples of treatments, for diseases or conditions treated by the compositions of the invention include, for example, but are not limited to, suppression of testosterone production, FSH, and LH for the treatment of prostate cancer and benign prostatic hyperplasia, directly blocking GnRH receptors on prostate cells for treatment of prostate cancer and benign prostatic hyperplasia, controlled ovarian stimulation for assisted reproductive techniques, treatment of uterine myoma, suppression of ovarian function while undergoing chemotherapy, treatment of breast cancer, treatment of ovarian cancer, male contraception, and female contraception.
As used herein, the terms “treat” and “treatment” refer to therapeutic treatment, including prophylactic or preventative measures, wherein the object is to prevent or slow down (lessen) an undesired physiological change associated with a disease or condition. Beneficial or desired clinical results include, but are not limited to, alleviation of symptoms, diminishment of the extent of a disease or condition, stabilization of a disease or condition (i.e., where the disease or condition does not worsen), delay or slowing of the progression of a disease or condition, amelioration or palliation of the disease or condition, and remission (whether partial or total) of the disease or condition, whether detectable or undetectable. “Treatment” can also mean prolonging survival as compared to expected survival if not receiving treatment. Those in need of treatment include those already with the disease or condition as well as those prone to having the disease or condition or those in which the disease or condition is to be prevented. The methods of treatment described herein can be used to treat any suitable mammal, including primates, such as monkeys and humans, horses, cows, cats, dogs, rabbits, elk, deer and rodents such as rats and mice. In one embodiment, the mammal to be treated is human.
“Administration” to a subject is not limited to any particular delivery system and may include, without limitation, parenteral (including subcutaneous, intravenous, intramedullary, intraarticular, intramuscular, or intraperitoneal injection).
The composition of the invention may be administered parenterally (e.g., intravenous, subcutaneous, intraperitoneal, and intramuscular). Further, the composition of the invention may be administered by intravenous infusion or injection. The composition of the invention may be administered by intramuscular or subcutaneous injection. In some embodiments, the composition of the invention may be administered surgically. As used herein, a “composition” refers to any composition that contains a pharmaceutically effective amount of one or more active ingredients (e.g., a GnRH antagonist). The composition, when administered to a subject (human or animal) induces a desired pharmacological and/or physiologic effect by local and/or systemic action.
The terms “subject,” “individual,” and “patient” are used interchangeably herein, and refer to an animal, for example a human, to whom treatment, including prophylactic treatment, with the pharmaceutical composition according to the present invention, is provided. The term “subject” as used herein refers to human and non-human animals. The terms “non-human animals” and “non-human mammals” are used interchangeably herein and include all vertebrates, e.g., mammals, such as non-human primates, (particularly higher primates), sheep, dog, rodent, (e.g. mouse or rat), guinea pig, goat, pig, cat, rabbits, cows, horses and non-mammals such as reptiles, amphibians, chickens, and turkeys.
All patents and literature references cited in the present specification are hereby incorporated by reference in their entirety.
Poly(DL-lactide-co-glycolide) with 50:50 ratio of lactide to glycolide can be dissolved in a suitable solvent to prepare an Atrigel® polymer solution. This solution can be filled into a syringe with a female luer lock fitting.
Each GnRH antagonist (ozarelix, degarelix, cetrorelix, or ganirelex) can be dissolved in water or other solvents and filled into a syringe with a male luer-lock fitting.
Prior to administration, the two syringes can be coupled, and the contents can be mixed back and forth between the two syringes for multiple cycles. After thorough mixing, the formulation can be drawn back into the syringe with the male coupling.
Then, the two syringes can be separated and a needle (a 21 G needle or smaller) can be attached. The contents of the syringe can then be subcutaneously injected into subjects. A total injection volume can be less than 4 mL.
Serum can be collected and analyzed. The GnRH antagonist composition may achieve a therapeutic effect within 24 hrs and maintain therapeutic effect for at least 90 days in >95% percent of treated patients.
The composition may allow for consistent release of the active agent from the drug delivery vehicle with no more than 25% variation plus an encapsulation efficiency of over 70%. The composition may release the active agent from the drug delivery vehicle with >85% intact over the entire duration of release.
A multi-block copolymer is provided. Each GnRH antagonist (ozarelix, degarelix, cetrorelix, or ganirelex) can be loaded into the multi-block copolymer. The formulation may be in the form of microspheres.
A syringe with a 21 G needle or smaller can be used to inject the formulation. The formulation can be subcutaneously injected into subjects. A total injection volume can be less than 4 mL.
Serum can be collected and analyzed. The GnRH antagonist composition may achieve a therapeutic effect within 24 hrs and maintain therapeutic effect for at least 90 days in >95% percent of treated patients.
The composition may allow for consistent release of the active agent from the drug delivery vehicle with no more than 25% variation plus an encapsulation efficiency of over 70%. The composition may release the active agent from the drug delivery vehicle with >85% intact over the entire duration of release.
Several formulations of microspheres using different polymers and internal water phase compositions were prepared for testing cetrorelix in vitro release (IVR). The tested formulations are summarized in Table 1.
The in vitro release of cetrorelix was tested by incubating microsphere formulations listed in Table 1 in 0.05 M Tris Buffer with 5% BSA, pH 7.4 at 37° C. The results show the release was slowest when premixed 35% Acetic acid/65% H2O as internal water phase was used (
To further test cetrorelix IVR several formulations of cetrorelix-loaded microspheres using different polymers and 35% Acetic acid/65% H2O as internal water phase were made (Table 2).
The in vitro release of cetrorelix was tested by incubating microsphere formulation listed in Table 2 in 0.05 M Tris Buffer with 5% BSA, pH 7.4 at 37° C. The results show that the RP17-014 formulation using 20LP10C20-LL40 polymer had the slowest cetrorelix release rate, and, in addition shown linear release kinetics (
These results show that slow degrading L-Lactide based polymers with low swellability are suitable for use in cetrorelix-loaded microspheres and display linear cetrorelix release. In addition, the microsphere manufacturing process achieves cetrorelix encapsulation of up to 15%.
Several salt-free cetrorelix-loaded microsphere formulations having different polymer contents were used for PK Study (Table 3). The preparations (<1 ml) were subcutaneously implanted into rats at a single 20 mg/kg dose and cetrorelix levels in plasma were monitored over 6 weeks. The results are summarized in Table 4 and
In addition, pharmacokinetics of cetrorelix microspheres formulations containing either Ca Pamoate or Na Oleate salt were tested in rats through subcutaneously implanting a single 5 mg/kg microspheres dose in a vehicle solution (20 mM K-Phos Buffer, 2.5% Mannitol, 3.5% CMC, 0.1% PS80) and monitoring cetrorelix levels in plasma over 6 weeks. The results are summarized in Table 5 and
There was no principal difference between pharmacokinetics of cetrorelix microspheres formulations containing Ca Pamoate and those containing Na Oleate both in the initial 24 hour burst release (
The downstream physiological effects of cetrorelix microspheres administration were assessed through monitoring testosterone levels in rats. All the formulations caused notable drop in serum testosterone levels (castration) after 24 hours (
The total amount of cetrorelix released was assessed using the method of Schwahn et al., Drug Metabolism & Disposition, Vol. 28, No. 1, p10, assuming rat weight ranging from 250 to 400 g, 10 mg/kg dose, and AUC (ng/mL*hr)=618.1.
Based on these assumptions, AUC for 20 mg/kg Dose (ng/mL*hr) was assumed to be 123,620 and AUC for 5 mg/kg Dose (ng/mL*hr) was assumed to be 30,905. The calculations based on the above assumptions results in estimated percentage of cetrorelix released (up to 42 days) ranging from 11 to 15% of the amount initially present in the microspheres. (See Table 6).
In order to supplement the in vivo pharmacokinetic data and further optimize the compositions of cetrorelix-loaded microspheres in vitro release studies were carried out wherein 45 mg of microspheres were incubated in 0.5 ml Tris Mannitol, pH 7.4 at 37° C. The results for in vitro release for the salt-free formulations used in pharmacokinetic studies are summarized in
In order to further explore the effect of salt and polymer on cetrorelix release, several formulations of salt-containing 15% RG502H (50:50 lactide:glycolide) and 15% RG752H (75:25 lactide:glycolide) (30% total PLGA content) cetrorelix-loaded microspheres (Table 7) were tested and compared with salt-free formulations.
The results show that the presence of salt markedly decreases cumulative cetrorelix release levels. While Na Oleate was particularly effective (
Surprisingly, when the polymer content was increased to 40% and replaced with
RG752H (75:25 lactide:glycolide) (Table 8) the presence of Ca Pamoate slowed the initial release rate but dramatically (nearly 3-fold) increased cumulative cetrorelix release, as compared with salt free formulation. On the other hand, similarly to RG502H/RG752H data, Na Oleate and Ca Citrate did not appear to have any effect on the initial release rate although these formulations displayed a modest increase in cumulative release levels (
In an attempt to investigate the effect of polymer and N-methyl-2-pyrrolidone (NMP) on cetrorelix release rate and cumulative release, microsphere formulations using 20% RG502H and 20% RG752H, or 40% RG752H, with and without NMP (Table 9) were tested.
The results are summarized in
Cetrorelix-Loaded Microspheres Pharmacokinetics (PK) in Rats
Several salt-free cetrorelix-loaded microsphere formulations having different polymer contents were used for PK Study (See Table 6 for PLGA content of salt-free cetrorelix-loaded microsphere formulations). The salt-free preparations (<1 ml) were subcutaneously implanted into rats at a single 20 mg/kg dose and cetrorelix levels in plasma were monitored over 17 weeks (119 days). The results are summarized in Table 11 and
In addition, pharmacokinetics of cetrorelix microspheres formulations containing either Ca Pamoate or Na Oleate salt were tested in rats through subcutaneously implanting a single 5 mg/kg microspheres dose in a vehicle solution (20 mM K-Phos Buffer, 2.5% Mannitol, 3.5% CMC, 0.1% PS80) and monitoring cetrorelix levels in plasma for 91 days. No plasma was collected after day 91 for rats into which cetrorelix microspheres formulations containing either Ca Pamoate or Na Oleate salt were implanted. (See Table 7 for salt-containing RG502H/RG752H (30% PLGA) cetrorelix-loaded microsphere formulations). The results are summarized in Table 11 and
There was no principal difference between pharmacokinetics of cetrorelix microspheres formulations containing Ca Pamoate and those containing Na Oleate both in the at the initial 24 hour burst release phase (
The downstream physiological effects of cetrorelix microspheres administration were assessed through monitoring testosterone levels in rats. All the formulations caused notable drop in serum testosterone levels after 24 hours (
The total amount of cetrorelix released was assessed using the method of Schwahn et al., Drug Metabolism & Disposition, Vol. 28, No. 1, p10, assuming rat weight ranging from 250 to 400 g, 10 mg/kg dose, and AUC (ng/mL*hr) =618.1.
Based on these assumptions, AUC for 20 mg/kg Dose (ng/mL*hr) was assumed to be 123,620 and AUC for 5 mg/kg Dose (ng/mL*hr) was assumed to be 30,905. The calculations based on the above assumptions results in estimated percentage of cetrorelix released (up to 119 days) ranging from 9 to 13% of the amount initially present in the microspheres. (See Table 11).
Several salt-free GnRH antagonist (e.g., cetrorelix) gel formulations are prepared as injectable suspension formulations having different GnRH antagonist content, PLGA polymer content and solvent content, e.g., N-methyl-2-pyrrolidone (NMP) in amounts shown in Table 12.
A dose level of 7.5 mg is given at the initial administration, at 1 month and at 2 months.
Poly(DL-lactide-co-glycolide) with 50:50 ratio of lactide to glycolide is dissolved in a suitable solvent to prepare an Atrigel® polymer solution. This solution is filled into a syringe with a female luer lock fitting. Alternatively, Poly(DL-lactide-co-glycolide) with 75:25 ratio of lactide to glycolide is dissolved in a suitable solvent to prepare an Atrigel® polymer solution. In another cetrorelix PLGA gel formulation, Poly(DL-lactide-co-glycolide) with 85:15 ratio of lactide to glycolide is dissolved in a suitable solvent to prepare an Atrigel® polymer solution.
Each GnRH antagonist (ozarelix, degarelix, cetrorelix, or ganirelex) can be dissolved in water or other solvents and filled into a syringe with a male luer-lock fitting.
Prior to administration, the two syringes can be coupled, and the contents can be mixed back and forth between the two syringes for multiple cycles. After thorough mixing, the formulation can be drawn back into the syringe with the male coupling.
Then, the two syringes can be separated and a needle (a 21G needle or smaller) can be attached. The contents of the syringe can then be subcutaneously injected into subjects. A total injection volume can be less than 4 mL. The injection mass may be 0.375 g of the 45 mg formulation once every six months. The injection mass may be 0.500 g of the 30 mg formulation once every four months. The injection mass may be 0.375 g of the 22.5 mg formulation once every three months. The injection mass may be 0.250 g of the 7.5 mg formulation once per month.
Serum can be collected and analyzed. The GnRH antagonist composition may achieve a therapeutic effect within 24 hours and maintain therapeutic effect for from at least 119 days to at least four months in >95% percent of treated patients. Therapeutic effect of the various salt-free GnRH antagonist gel formulations is assessed through monitoring testosterone levels in the patients, as well as size of the prostate. All the formulations cause a notable drop in serum testosterone levels after 24 hours of less than or equal to 50 ng/mL. Moreover, the formulations cause a notable drop in serum testosterone levels after 24 hours of less than or equal to 10 ng/mL. These low human testosterone levels are comparable to the low serum testosterone demonstrated in rat studies (
It will be appreciated by those skilled in the art that changes could be made to the embodiments described above without departing from the broad inventive concept thereof. It is understood, therefore, that this invention is not limited to the particular embodiments disclosed, but it is intended to cover modifications that are within the spirit and scope of the invention, as defined by the appended claims.
This application is a continuation-in-part application of U.S. patent application Ser. No. 15/885,464, filed Jan. 31, 2018, which claims priority to and the benefit of U.S. Provisional Patent Application 62/452,788, filed Jan. 31, 2017, both of which are incorporated by reference herein in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62452788 | Jan 2017 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15885464 | Jan 2018 | US |
| Child | 15974461 | US |
