Patent Application
20080152704
The present invention relates to palonosetron, and especially to solid oral dosage forms of palonosetron hydrochloride that meet demanding shelf stability requirements.
The nausea and emetogenic side effects of anti-cancer chemotherapy and radiotherapy are a widespread and longstanding problem. Perhaps less well known but no less important are post-operative nausea and emesis, which may have physiological mechanisms related to the effects seen for chemotherapy. Palonosetron hydrochloride has recently emerged as a highly efficacious anti-nauseant and anti-emetic for use with emetogenic anti-cancer chemotherapies. (Nacciocchi, A., et al., “A Phase II dose-ranging study to assesses single intravenous doses of palonosetron for the prevention of highly emetogenic chemotherapy-induced nausea and vomiting,” Proc. Am. Soc. Clin. Oncol., 2002; Abstract 1480. Palonosetron also prevents postoperative nausea and vomiting. (Chelly, J., et al., “Oral RS-25259 prevents postoperative nausea and vomiting following laparoscopic surgery,” Anesthesiol., 85(Suppl. 21):abstract no. 3A (1996)). Methods of treating chemotherapy induced nausea and vomiting (CINV) and radiation induced nausea and vomiting (RINV) with palonosetron are described in PCT publication WO 2004/045615 from Helsinn Healthcare SA. Methods of treating post-operative nausea and vomiting (PONV) with palonosetron are described in PCT publication 2004/073714, also from Helsinn Healthcare SA.
Palonosetron is selective, showing a high affinity as an antagonist for the 5-hydroxyltryptamine 3 receptor precursor (5-HT3 receptor), and showing a low affinity for other receptors such as dopamine receptors (Wong, E. H. F., et al., “The interaction of RS 25259-197, a potent and selective antagonist, with 5-HT3 receptors, in vitro,” Br. J. Pharmacol., 114:851-859 (1995); Eglen, R. M., et al., “Pharmacological characterization of RS 25259-197, a potent and selective antagonist, with 5-HT3 receptors, in vivo,” Br. J. Pharmacol., 114:860-866 (1995)). Palonosetron is a synthetic compound existing as a single isomer, and is administered as the hydrochloride salt, as represented in the following structure:
The official chemical name for the drug is (3aS)-2-[(S)-1-Azabicyclo [2.2.2]oct-3-yl]-2,3,3a,4,5,6-hexahydro-1-oxo-1Hbenz[de] isoquinoline hydrochloride (CAS No. 119904-90-4); its empirical formula is C19H24N2O.HCl, and its molecular weight is 332.87. Methods of synthesizing the compound are described in U.S. Pat. Nos. 5,202,333 and 5,510,486.
Palonosetron hydrochloride is sold as a sterile injectable liquid in the United States as ALOXI® by MGI Pharma and Helsinn Healthcare SA. The intravenous liquid is clear, colorless, non-pyrogenic, in an isotonic, buffered solution. A stable isotonic solution of palonosetron for injection is described in Helsinn's PCT publication WO 2004/067005.
Despite the numerous clinical benefits and advantages of this intravenous formulation, it is generally recognized that injection drug delivery systems present special problems with respect to storage life and stability of the active agent. They are also inconvenient when self administered, and have increased risk of contamination and human error. Thus an oral delivery option for palonosetron, especially in solid form, would be particularly attractive. Methods for improving the stability and shelf-life of palonosetron formulations would also be desirable.
Soft-gel capsules of palonosetron have been developed that exhibit excellent bioavailability when orally ingested, and stability when stored for prolonged periods of time. The outer shell for the capsule is gelatin based, and the inner fill for the capsule is a continuous lipophilic inner phase that contains palonosetron dissolved in an aqueous component, miscibilized or homogenized in the lipophilic phase by minimal quantities of a surfactant. The formulation represents an elegant solution to the tension commonly observed between:
In a first principal embodiment, therefore, the invention provides a soft gelatin capsule for oral administration comprising: (a) a soft gelatin outer shell having an oxygen permeability of less than about 1.0×10−3 ml·cm/(cm2·24 hr. atm); and (b) a lipophilic liquid inner fill composition comprising: (i) greater than about 50 wt. % of one or more lipophilic components; (ii) from about 1 to about 20 wt. % of water miscibilized or homogenized in said one or more lipophilic components; (iii) from about 0.05 to about 2.0 mg. of palonosetron as palonosetron hydrochloride solubilized or dispersed in said water; and (iv) from about 0.5 to about 5 wt. % of a surfactant.
Formulations and methods of manufacture have also been developed that can be defined by the amount or concentration of palonosetron in the dosage form, and the degradation byproducts within the dosage form. One such degradation by product is an oxygen mediated degradation product, and is referred to herein as “Cpd1.”
Dosage forms of palonosetron, including methods of manufacture, have also been developed with enhanced stability due to their protection from oxygen and oxygen mediated degradation. Based on these discoveries and developments, dosage forms have been developed that can be defined by one or more of the following physical features:
These dosage forms have excellent stability over prolonged periods of time, excellent resistance to oxidative degradation, and excellent bioavailability when orally ingested. These dosage forms can be used in the treatment of any disease for which palonosetron has clinical utility, but they are preferably used for the treatment of emesis.
In a second principal embodiment, therefore, the invention provides a capsule dosage form for oral administration comprising: (a) an outer shell having a oxygen permeability of less than about 1.0×10−3 ml·cm/(cm2·24 hr. atm); and (b) an inner fill composition comprising: from about 0.05 to about 2.0 mg. of palonosetron as palonosetron hydrochloride, wherein said palonosetron comprises Cpd1 in an amount of less than 1.0 wt. %; wherein no more than 5.0 wt. % of said palonosetron hydrochloride degrades when said dosage form is stored three months or greater at 40° C. and 75% RH.
Of course, the invention could be practiced using dosage forms other than capsules, and in another embodiment the invention provides a solid oral dosage form comprising: (a) an outer shell or coating having a oxygen permeability of less than about 1.0×10−3 ml·cm/(cm2·24 hr. atm); and (b) an inner fill composition comprising: from about 0.05 to about 2.0 mg. of palonosetron as palonosetron hydrochloride, wherein said palonosetron comprises Cpd1 in an amount of less than 1.0 wt. %; wherein no more than 5.0 wt. % of said palonosetron hydrochloride degrades when said dosage form is stored three months or greater at 40° C. and 75% RH.
Methods have also been developed for manufacturing palonosetron dosage forms that have reduced quantities of impurities and oxygen mediated degradation products, and to palonosetron dosage forms manufactured by these methods. Thus, in still another embodiment the invention provides a method for manufacturing a batch of palonosetron dosage forms having reduced quantities of impurities and oxygen mediated degradation products comprising (a) mixing palonosetron hydrochloride and one or more pharmaceutically acceptable excipients to form a mixture; (b) processing said mixture into a plurality of final dosage forms; and (c) testing one or more of said final dosage forms for Cpd1. This method can be practiced with any dosage form, including a capsule, gel-cap or liquid filled ampoule.
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 may 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.
Both figures report arithmetic mean plasma concentrations of palonosetron (ng/ml) versus time (H) on a linear scale (n=33).
The present invention may be understood more readily by reference to the following detailed description of preferred embodiments of the invention and the Examples included therein.
As used in this specification and in the claims which follow, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “an ingredient” includes mixtures of ingredients, reference to “an active pharmaceutical agent” includes more than one active pharmaceutical agent, and the like.
“Treating” or “treatment” of a disease includes (1) preventing the disease from occurring in an animal that may be predisposed to the disease but does not yet experience or display symptoms of the disease, (2) inhibiting the disease, i.e. arresting its development, or (3) relieving the disease, i.e. causing regression of the disease.
As used herein, an ambient environment refers to the environment immediately surrounding an element or process, typically a gaseous environment, with which the element or process is in contact and communication.
“Emesis,” for the purposes of this application, will have a meaning that is broader than the normal, dictionary definition and includes not only vomiting, but also nausea and retching.
“Moderately emetogenic chemotherapy” refers to chemotherapy in which the emetogenic potential is comparable or equivalent to the emetogenic potential of carboplatin, cisplatin ≦50 mg/m2, cyclophosphamide <1500 mg/m2, doxorubicin >25 mg/ms, epirubicin, irinotecan, or methotrexate >250 mg/m2.
“Highly emetogenic chemotherapy” refers to chemotherapy in which the emetogenic potential is comparable or equivalent to the emetogenic potential of cisplatin ≧60 mg/m2, cyclophosphamide >1500 mg/m2, or dacarbazine.
“Pharmaceutically acceptable” means that which is useful in preparing a pharmaceutical composition that is generally safe, non-toxic and neither biologically nor otherwise undesirable and includes that which is acceptable for veterinary use as well as human pharmaceutical use.
“Therapeutically effective amount” means that amount which, when administered to an animal for treating a disease, is sufficient to effect such treatment for the disease.
A “de minimis” quantity of oxygen refers to an amount of oxygen that allows no more than about 0.5, 1.0, 1.5, 2.0, 2.5, or 3.0 wt. % of said palonosetron to degrade (preferably defined by degradation to Cpd1) when stored at room temperature under ambient conditions for six, twelve, eighteen, twenty-four, thirty or thirty-six months.
Shelf stability, for purposes of this invention, is measured by storing the dosage form in its packaging at 40° C., at a relative humidity of 75%, or under ambient conditions, for three, six, twelve, eighteen, twenty-four, thirty or thirty-six months. A stable formulation is one in which no more than about 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, or 5.0 wt. % of the palonosetron in the dosage form degrades (preferably defined by degradation to one or more of the degradation products described herein).
When ranges are given by specifying the lower end of a range separately from the upper end of the range, it will be understood that the range can be defined by selectively combining any one of the lower end variables with any one of the upper end variables that is mathematically possible.
When used herein the term “about” or “ca.” will compensate for variability allowed for in the pharmaceutical industry and inherent in pharmaceutical products, such as differences in product strength due to manufacturing variation and time-induced product degradation. The term allows for any variation which in the practice of pharmaceuticals would allow the product being evaluated to be considered bioequivalent to the recited strength of a claimed product.
The term “absolute bioavailability” refers to the availability of the active drug in systemic circulation after non-intravenous administration (i.e., after oral, rectal, transdermal, subcutaneous administration). In order to determine absolute bioavailability of a drug, a pharmacokinetic study must be done to obtain a plasma drug concentration versus time plot for the drug after both intravenous (IV) and non-intravenous administration. The absolute bioavailability is the dose-corrected area under curve (AUC) non-intravenous divided by AUC intravenous. A formulation is said to be bioequivalent in terms of absolute bioavailability to a reference formulation when there is established a 90% confidence interval for AUC(0-∞) which is between 80% and 125%, relative to degree of bioavailability for the reference formulation.
When pharmacokinetic parameters are given herein (i.e. Tmax, absolute bioavailability, etc.), it will be understood that they can refer to the mean, median, or individual observed pharmacokinetics, and that mean pharmacokinetics are intended when claimed unless stated to the contrary. The pharmacokinetic parameter will also be understood to be observed in the fasted state, unless otherwise stated.
As mentioned above, the invention provides solid oral dosage forms that have improved stability and resistance to oxidative degradation, based on several formulation techniques, including the use of a coating or shell that is substantially impermeable to oxygen, or the use of a lipophilic liquid filling having water homogenized or miscibilized therein. In a first principal embodiment the invention provides a solid oral dosage form comprising: (a) an outer shell or coating having a oxygen permeability of less than about 1.0×10−3 ml·cm/(cm2·24 hr. atm); and (b) an inner fill composition comprising: from about 0.05 to about 2.0 mg. of palonosetron as palonosetron hydrochloride, wherein said palonosetron comprises Cpd1 in an amount of less than 1.0 wt. %; wherein said dosage form exhibits shelf stability, preferably defined so that no more than 5.0 wt. % of said palonosetron hydrochloride degrades when said dosage form is stored three months or greater at 40° C. and 75% RH. The invention further provides a method of treating emesis comprising orally administering to a patient suffering from emesis, or at risk for suffering emesis, a dosage form of the present invention.
The invention can be practiced with any type of solid oral dosage form, defined as any dosage form that is administered via the oral route and swallowed including, for example, a capsule or gel-cap (i.e. a liquid filled capsule). In a preferred embodiment the dosage form is a capsule, and in an even more preferred embodiment the dosage form is a liquid filled gel-cap.
Whatever the dosage form, it preferably has an outer shell or coating that has minimal oxygen permeability. In preferred embodiments of the invention, the coating or shell has an oxygen permeability that is less than about 1.0×10−3, 5.0×10−4, 1.0×10−4, 5.0×10−5, or even 2.0×10−5 ml·cm/(cm2·24 hr. atm).
A preferred dosage form for the present invention is a capsule having an outer shell that dissolves in gastric fluids. A liquid-filled capsule, preferably including water, is especially preferred because of the uniformity of content and dose when working with liquids, and the ability to minimize oxygen exposure while manufacturing the dosage form and storing the dosage form for prolonged periods of time.
Of the available outer shells, a soft outer shell is a preferred shell structure because of its ability to hold liquids and resist oxygen transmission. Preferred materials for the outer “gel-cap” shell include, for example, gelatin, cellulose, starch, or HPMC. In a preferred embodiment, the shell comprises gelatin, and optionally one or more shell excipients selected from glycerin, sorbitol and titanium dioxide.
The liquid composition that fills the capsule is preferably (1) predominantly lipophilic, and (2) present as a continuous liquid phase (i.e. wherein the liquid components are either miscible or completely homogenized/emulsified). A continuous phase is preferred for ease of processing and composition uniformity. The liquid fill includes the excipient base and the active agent evenly distributed throughout the liquid fill. Furthermore, the active agent is preferably dissolved or dispersed as a microemulsion in the excipient base. The total weight of the fill composition may range is preferably greater than about 50, 75, or 100 mg, and is preferably less than about 500, 250, 200, or 150 mg, most preferably from about 100 to about 150 mg.
The liquid fill is preferably composed predominantly of one or more lipophilic components in an amount of from about 50 wt. % to about 99 wt. %, preferably from about 75 wt. % to about 98 wt. %. Preferred lipophilic components include, for example, mono- and di-glycerides of fatty acids, especially including the mono- and di-glycerides of capryl/capric acid. The liquid fill may also contain glycerin, preferably in an amount of from about 1 to about 15 wt. %, more preferably from about 2 to about 10 wt. %. In one preferred embodiment, both the shell and the inner fill composition comprise glycerin. In another preferred embodiment, the liquid fill comprises 0.25, 0.35 mg. or more of palonosetron as palonosetron hydrochloride (i.e. 0.50 or 0.75 mg.); solubilized in a solubilizing effective amount of a liquid comprising a lipophilic excipient and water.
The fill composition may comprise various means to facilitate the transition of palonosetron from the dosage form to the gastrointestinal fluids of the GI tract, so that the palonosetron may be more readily absorbed into the bloodstream. For example, the liquid fill composition may contain a surfactant, optimally in an amount of from about 0.1 wt. % to about 6 wt. %, from about 0.5 wt. % to about 5 wt. %, or from about 1.0 wt. % to about 3.0 wt. %. The liquid fill composition preferably comprises greater than 0. 1, 0.5, or 1.0 wt. % of surfactant, and less than 10, 8, 5, 4, or even 4 wt % of surfactant. A particularly preferred surfactant is polyglyceryl oleate.
Alternatively or in addition, the transitioning means for a liquid filled capsule may comprise water that forms a single phase or microemulsion with the other liquid ingredients in the excipient base. The liquid fill composition preferably comprises from about 0.05 wt. % to about 30 wt. % water, from about 1 wt. % to about 20 wt. % water, or from about 2 wt. % to about 10 wt. % water. The liquid fill preferably comprises greater than 0.1, 0.5 or 1.0 wt. % water, and less than 20, 15, 10, 8 or 5 wt. % water.
Still further, the excipient base may contain one or more chemical agents to prevent oxygen mediated degradation of the palonosetron in the dosage form. For example, the excipient base may contain a chelating agent such as ethylenediamine tetraacetic acid (EDTA), an antioxidant such as butylated hydroxyanisole (BHA), or a reducing agent, in an amount ranging from about 0.005 wt % to about 2.0 wt. %, more preferably from about 0.01 wt. % to about 1.0 wt. % or from about 0.05 wt. % to about 0.5 wt. %. In a preferred embodiment the excipient base contains an antioxidant.
The active agent, which is preferably palonosetron hydrochloride, is preferably present in the fill composition in an amount ranging from about 0.01 to about 10.0 wt. %, from about 0.05 to about 5.0 wt. %, or from about 0.1 wt % to about 2.0 wt. %. Alternatively, particularly stable formulations have been found where the concentration of palonosetron exceeds 0.3%, preferably at a concentration no greater than about 1 wt. %.
A particularly important feature of the inner fill composition, which is preferred in any of the embodiments of this invention, regardless of dosage form or fill type or method of manufacture, is the minimal content of oxygen. In a preferred embodiment, the inner fill composition comprises oxygen in an amount that degrades no more than about 3.0 wt. %, 2.5 wt. %, 2.0 wt. %, 1.5 wt. %, 1.0 wt. %, or 0.5 wt. %, of said palonosetron, when the dosage form is stored under shelf stability testing regimens, for example for three months at 40° C. and 75% RH. This amount is preferably measured by the amount of Cpd1 in the composition.
Another important feature of the formulations of the present invention is their pharmacokinetics. It has been determined that the dosage forms of the current invention have an absolute bioavailability of approximately 100%, within the limits of bioequivalence. Thus, for example, whereas a 0.75 mg injection of palonosetron yields a mean AUC(0-∞) of ca. 58285 (ng·hr/L), a 0.75 mg gel cap yields a mean AUC(0-∞) of ca. 57403 (ng·hr/L). In contrast, the mean Cmax for a 0.75 mg gel cap is about 1224 ng/L, whereas a 0.75 mg. injection yields a mean Cmax of about 1665 ng/L. A 0.50 mg gel cap has been shown to yield a mean AUC(0-∞) of ca. 38176 (ng·hr/L), and a mean Cmax of about 810 ng/L, thereby demonstrating dose proportionate pharmacokinetics.
In various embodiments, therefore, the dosage form of the present invention yields greater than 90, 95, or even 98 % absolute bioavailability as an arithmetic mean, again within the limits of bioequivalence. Alternatively or in addition, a 50 mg gel cap yields a mean Cmax of from about 700 to about 950 ng/ml, or from about 750 to about 875 ng/ml. In a most preferred embodiment, a 50 mg gel gap yields a Cmax of from 800 to 820 ng/L, preferably within the limits of bioequivalence. Because the dosage forms of the present invention demonstrate dose proportionate pharmacokinetics, it will be understood that these Cmax values can be standardized based on the strength of the dosage form, and that Cmax values can be assigned to alternative strengths based upon such standardization.
Yet another important feature of the dosage forms of the present invention, which also is preferred in any of the embodiments of the present invention, pertains to the dissolution of the dosage form, and in a preferred embodiment no less than about 75% of the palonosetron in the dosage form dissolves in 30 or 45 minutes when tested in a type II paddle dissolution apparatus according to the U.S. Pharmacopeia, at 75 rpm and 37° C., in 500 ml. of 0.01N HCl.
Still another feature of the dosage forms of the present invention, which is also preferred in any of the embodiments of the present invention, regardless of dosage form or fill type or method of manufacture, is that the dosage form experiences no more than 5 wt. %, 3 wt. %, or 2 wt. % degradation of the palonosetron when the dosage form in its moisture resistant packaging is exposed to an environment of 25° C. and 60% RH, or 40° C. and 75% RH, for periods equal to or exceeding 3 months, six months, 9 months or even one year.
The palonosetron used in the present invention can be palonosetron as a base or pharmaceutically acceptable salt, but is preferably palonosetron hydrochloride. In addition, the palonosetron is preferably present in an amount ranging from about 0.02 mg. to about 10 mg. per dosage form, more preferably from about 0.05 or 0.15 to about 2 mg. per dosage form, and still more preferably from about 0.2 to about 1.0 mg. per dosage form, based on the weight of the base when present as a pharmaceutically acceptable salt. Particularly preferred doses are 0.25 mg, 0.50, and 0.75 mg. of palonosetron or salt thereof, based on the weight of the base. Particularly stable formulations have been found by using palonosetron amounts in liquid gel-caps of greater than about 0.25, 0.35 or 0.45 mg., preferably less than about 2.0 mg.
The palonosetron hydrochloride used to make the dosage form, or contained in the final dosage form, may also be characterized by the presence of various palonosetron related compounds, including compounds Cpd3, Cpd2, and/or Cpd1, as described by the following chemical structures:
Compounds Cpd2 and Cpd3 are typically present, on an individual or combined basis relative to the palonosetron hydrochloride, in amounts of less that 1.0 wt. %, 0.75 wt. % or 0.5 wt. %, and/or greater than about 0.05 wt. %, 0.075 wt. % or 0.1 wt. %. Cpd2 and Cpd3 can be measured in the dosage form or in the palonosetron raw material used to make the dosage form. Compound Cpd1 is typically present, on an individual basis relative to the palonosetron hydrochloride, in an amount greater than about 0.05 wt. %, 0.1 wt. % or 0.2 wt. %, and/or less than about 3.0 wt. %, 2.5 wt. %, 2.0 wt. %, 1.5 wt. %, 1.0 wt. %, or 0.5 wt. %. Cpd1 is preferably measured in the dosage form since it is a measure of oxygen mediated degradation. In one preferred embodiment, the dosage forms are defined by a stability in which no more than about 5.0 wt. %, 4.0 wt. %, 3.0 wt. %, 2.5 wt. %, 2.0 wt. %, 1.5 wt. %, 1.0 wt. %, or 0.5 wt. % of compound Cpd1, are formed when the dosage form in its moisture resistant packaging is exposed to an environment of 25° C. and 60% RH, or 40° C. and 75% RH, for periods equal to or exceeding 3 months, 6 months, 9 months or even one year.
Therefore, in another embodiment the invention provides a solid oral dosage form comprising: (a) from about 0.05 to about 2.0 mg. of palonosetron or a pharmaceutically acceptable salt thereof; (b) one or more pharmaceutically acceptable excipients; (c) Cpd1 in an amount less than 3.0 wt. % based on the weight of the palonosetron. In another embodiment the invention provides a solid oral dosage form comprising: (a) from about 0.05 to about 2.0 mg. of palonosetron or a pharmaceutically acceptable salt thereof; (b) one or more pharmaceutically acceptable excipients; (c) Cpd2 or Cpd3, in an amount less than 1.0 wt. %, based on the weight of the palonosetron or pharmaceutically acceptable salt thereof. In either of these embodiments, the dosage form may optionally comprise means for preventing oxygen mediated degradation of said palonosetron.
Other palonosetron related compounds that can be present in the compositions include Cpd4, Cpd5, Cpd6 and Cpd7, as depicted below:
The invention also provides methods of making palonosetron dosage forms. Thus, in still another embodiment the invention provides a method for manufacturing a batch of palonosetron dosage forms having reduced quantities of impurities and oxygen mediated degradation products comprising (a) mixing palonosetron hydrochloride and one or more pharmaceutically acceptable excipients to form a mixture; (b) processing said mixture into a plurality of final dosage forms; and (c) testing one or more of said final dosage forms for one or more palonosetron related compounds selected from Cpd2, Cpd1, and Cpd3. “Processing” refers to the steps used to prepare a pharmaceutical formulation and final dosage form from a defined set of ingredients, and excludes the processes of chemically synthesizing the ingredients used in the formulation. This embodiment extends to all dosage forms of palonosetron, including single unit dose ampoules of palonosetron filled, for example, with a sterile injectable liquid. Thus, for example, the invention may be extended to methods for filling unit dose ampoules or containers with sterile injectable solutions of palonosetron, preferably in aqueous media, and preferably formulated as described in WO 2004/067005 of Calderari et al. In this context, an “ampoule” means a small sealed container of medication that is used one time only, and includes breakable and non-breakable glass ampoules, breakable plastic ampoules, miniature screw-top jars, and any other type of container of a size capable of holding only one unit dose of palonosetron (typically about 5 mls.).
Another embodiment captures the balance achieved by the formulations of the present invention, relative to bioavailability and stability, and in this embodiment the invention provides a method of optimizing the bioavailability and stability of palonosetron in a palonosetron gelatin capsule comprising: (a) providing a soft gelatin outer shell having an oxygen permeability of less than about 1.0×10−3 ml·cm/(cm2·24 hr. atm); and (b) preparing a fill composition by steps comprising: (i) providing from about 0.05 to about 2.0 mg. of palonosetron as palonosetron hydrochloride, wherein said palonosetron comprises Cpd1 in an amount of less than 1.0 wt. % based on the weight of said palonosetron; (ii) dissolving or dispersing said palonosetron in water to form an aqueous premix; (iii) mixing said aqueous premix with one or more lipophilic excipients, at a weight ratio of aqueous premix to lipophilic excipients of less than 50:50. 40:60, 30:70, or 20:80, to form a miscible or homogenous lipophilic fill composition; (iv) mixing a surfactant with said water, said aqueous premix, or said fill composition; and (v) balancing the quantities of surfactant and water in said fill composition to facilitate the bioavailability of palonosetron from said gelatin capsule when orally ingested, and to minimize the degree of palonosetron degradation; and (c) filling said outer shell with said fill composition.
Still another method of the present invention comprises a method of packaging a palonosetron dosage form comprising: (a) providing an empty shell; and (b) filling said shell container with a fill composition in an oxygen depleted ambient environment, wherein said fill composition comprises: (i) a defined amount of an active ingredient composition comprising palonosetron or a pharmaceutically acceptable salt thereof; and (ii) a pharmaceutically acceptable excipient. An “oxygen depleted environment” is preferably one defined by an oxygen content of less than about 10% oxygen, 5% oxygen, or even 1% or 0.1% oxygen (on a weight or volume basis). In an even more preferred embodiment, the methods of making or packaging the dosage forms of the present invention are performed under a nitrogen blanket or purge, in a nitrogen rich environment comprising greater than about 90%, 95%, or 98% nitrogen (on a weight or volume basis).
In another particular embodiment, the method is defined by the variability of active ingredient among dosage forms, in which there is provided a method of making a plurality of solid oral dosage forms comprising: (a) providing a capsule shell; (b) filling said shell with a fill composition comprising: (i) a defined amount of palonosetron or a pharmaceutically acceptable salt thereof; and (ii) a pharmaceutically acceptable excipient; and (c) repeating steps (a) and (b) one or more additional times, wherein said defined amount has a capsule to capsule variability of less than about 3, 2, 1, 0.5 or 0.1 wt. %.
In any of the foregoing embodiments, the method of making may also further comprise packaging said dosage form or plurality of dosage forms in a moisture resistant sealed container. The material used to form the moisture resistant sealed container preferably has an oxygen permeability less than about 1.0×10−2, 1.0×10−3, 1.0×10−4, or even 5.0×10−5 ml·cm/(cm2·24 hr. atm). Alternatively or in addition, the packaging can be characterized as a “tight container” under standards described in USP <671> (i.e. not more than one of ten test containers exceeds 100 mg. per day per L in moisture permeability, and none exceeds 200 mg. per day per ml.). Still further, the container can be defined by the amount of moisture that it allows the dosage forms of the invention to absorb during storage. For example, in various preferred embodiments, the container prevents said doses from absorbing more than 1.0, 0.1 or even 0.05 wt. % moisture in three months when stored at 40° C. and 75% relative humidity. Blister packaging is a particularly preferred mode of packaging.
The liquid core pharmaceutical compositions of the present invention are encapsulated in a soft gelatin shell described below. Gelatin is a preferred component of the soft gelatin shells of the instant invention. The starting gelatin material may be obtained by the partial hydrolysis of collagenous material, such as the skin, white connective tissues, or bones of animals. Gelatin material can be classified as Type A gelatin, which is obtained from the acid-processing of porcine skins and exhibits an isoelectric point between pH 7 and pH 9; and Type B gelatin, which is obtained from the alkaline-processing of bone and animal (bovine) skins and exhibits an isoelectric point between pH 4.7 and pH 5.2. Blends of Type A and Type B gelatins can be used to obtain a gelatin with the requisite viscosity and bloom strength characteristics for capsule manufacture. Gelatin suitable for capsule manufacture is commercially available from the Sigma Chemical Company, St. Louis, Mo. For a general description of gelatin and gelatin-based capsules, see Remington's Pharmaceutical Sciences, 16th ed., Mack Publishing Company, Easton, Pa. (1980), page 1245 and pages 1576-1582; and U.S. Pat. No. 4,935,243, to Borkan et at., issued Jun. 19, 1990; these two references being incorporated herein by reference in their entirety.
The soft gelatin shells may comprise from about 20% to about 60% gelatin. The gelatin can be of Type A or Type B, or a mixture thereof with bloom numbers ranging from about 60 to about 300. The soft gelatin shells may also comprise a plasticizer. Useful plasticizers include glycerin, sorbitan, sorbitol; or similar low molecular weight polyols, and mixtures thereof. A preferred plasticizer useful in the present invention is glycerin. The soft gelatin shells of the instant invention may also comprise water. Without being limited by theory, the water is believed to aid in the rapid dissolution or rupture of the soft gelatin shell upon contact with the gastrointestinal fluids encountered in the body.
Soft gelatin capsules and encapsulation methods are described in P. K. Wilkinson et at., “Softgels: Manufacturing Considerations”, Drugs and the Pharmaceutical Sciences, 41 (Specialized Drug Delivery Systems), P. Tyle, Ed. (Marcel Dekker, Inc., New York, 1990) pp. 409-449; F. S. Horn et at., “Capsules, Soft”, Encyclopedia of Pharmaceutical Technology, vol. 2, J. Swarbrick and J. C. Boylan, eds. (Marcel Dekker, Inc., New York, 1990) pp. 269-284; M. S. Patel et at., “Advances in Softgel Formulation Technology”, Manufacturing Chemist, vol. 60, no. 7, pp. 26-28 (July 1989); M. S. Patel et al., “Softgel Technology”, Manufacturing Chemist, vol. 60, no. 8, pp. 47-49 (August 1989); R. F. Jimerson, “Softgel (Soft Gelatin Capsule) Update”, Drug Development and Industrial Pharmacy (Interphex '86 Conference), vol. 12, no. 8 & 9, pp. 1133-1144 (1986); and W. R. Ebert, “Soft Elastic Gelatin Capsules: A Unique Dosage Form”, Pharmaceutical Technology, vol. 1, no. 5, pp. 44-50 (1977); these references are incorporated by reference herein in their entirety. The resulting soft gelatin capsule is soluble in water and in gastrointestinal fluids. Upon swallowing the capsule, the gelatin shell rapidly dissolves or ruptures in the gastrointestinal tract thereby introducing the pharmaceutical actives from the liquid core into the body.
In still further embodiments, the invention provides methods of treating emesis by administering one or more of the dosage forms described herein. The emesis may be acute phase emesis (i.e. emesis experienced within about 24 hours of an emesis inducing event), or delayed emesis (i.e. emesis experienced after the acute phase, but within seven, six, five or four days of an emesis inducing event). The emesis may constitute chemotherapy induced nausea and vomiting (“CINV”), from moderately or highly emetogenic chemotherapy, radiation therapy induced nausea and vomiting (“RINV”), or post-operative nausea and vomiting (“PONV”).
When a product is said to exhibit a particular pharmacokinetic parameter “within the limits of bioequivalence,” it will be understood that the product is bioequivalent to a test drug employing the bioequivalence testing specified herein. Bioequivalence testing typically requires an in vivo test in humans in which the concentration of the active ingredient or active moiety, and, when appropriate, its active metabolite(s), in whole blood, plasma, serum, or other appropriate biological fluid is measured as a function of time. Defined as relative bioavailability (“BA”), bioequivalence (“BE”) involves a comparison between a test and reference drug product. Although BA and BE are closely related, BE comparisons normally rely on (1) a criterion, (2) a confidence interval for the criterion, and (3) a predetermined BE limit.
A standard in vivo BE study design is based on the administration of either single or multiple doses of the test and reference products to healthy subjects on separate occasions, with random assignment to the two possible sequences of drug product administration. Statistical analysis for pharmacokinetic measures, such as area under the curve (AUC) and peak concentration (Cmax), is preferably based on the so-called “two one-sided tests procedure” to determine whether the average values for the pharmacokinetic measures determined after administration of the test and reference products are comparable. This approach is termed average bioequivalence and involves the calculation of a 90% confidence interval for the ratio of the averages (population geometric means) of the measures for the test and reference products. To establish BE, the calculated confidence interval should fall within a BE limit, i.e. 80-125% for the ratio of the product averages. Thus, for example, bioequivalence is said to be established under a given set of circumstances by a 90% confidence interval for AUC which is between 80% and 125%, and a 90% confidence interval for Cmax which is between 80% and 125%.
Further detail regarding BE procedures can be found in FDA's July 1992 Guidance Document entitled “Statistical Procedures for Bioequivalence Studies Using a Standard Two-Treatment Crossover Design,” the contents of which are incorporated herein by reference.
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 claimed herein are made and evaluated, and are intended to be purely exemplary of the invention and are not intended to limit the scope of what the inventors regard as their invention. 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 room temperature, and pressure is at or near atmospheric
Table 1 describes representative formulations for a gel-cap solid oral dosage form containing 0.25, 0.50 and 0.75 mg. of palonosetron.
acorresponding to 0.25 mg free base
bcorresponding to 0.50 mg free base
ccorresponding to 0.75 mg free base
The compounding process involves the formulation of two separate mixes, the side mix containing the active ingredient, glycerin and water, and the main mix containing the remaining excipients. The process starts with the two separate mixes which are later combined to comprise the final fill solution for encapsulation. The fill solution is blanketed with nitrogen during the compounding and encapsulation phases.
An exemplary dissolution method for Palonosetron Oral Capsules, 0.25 mg, 0.50 mg, and 0.75 mg uses USP Apparatus 2 (paddles) at 75 rpm in 500 mL of 0.01N HCl with a dissolution temperature of 37.0±0.5° C. The acceptance criterion is “Not less than 75% at 45 minutes”.
Six softgel-capsules are individually weighed. Softgel-capsules are placed in each vessel, and sampled at 15, 30, 45, and 60 minutes. Sampling at 15, 30, 60 minutes is for information only. Sample solutions are withdrawn and filtered through online filters into test tubes or HPLC vials. The samples are analyzed using a HPLC system with UV detector.
Table 3 presents the results of chemical and physical stability testing for the 0.75 mg. palonosetron softgel formulations reported in Example 1, packaged in a 2×5 Blister Unit (Forming: LM 15088, Foil: Reynolds 701).
Table 4 presents the results of chemical and physical stability testing for the 0.50 mg. palonosetron softgel formulations reported in Example 1, packaged in a 2×5 Blister Unit (Forming: LM 15088, Foil: Reynolds 701).
Table 5 presents the results of chemical and physical stability testing for the 0.25 mg. palonosetron softgel formulations reported in Example 1, packaged in a 2×5 Blister Unit (Forming: LM 15088, Foil: Reynolds 701).
The following Table 6 describes a representative injectable formulation containing palonosetron.
Bioequivalence and absolute bioavailability were tested in a single oral dose of two formulations of 0.75 mg palonosetron in healthy volunteers. The study was aa three treatment, three period, two sequence cross-over study.
Treatment A represented a single dose of 0.75 mg of palonosetron in the clinical gel-cap formulation described in Table 1.
Treatment B represented a single dose of 0.75 mg of palonosetron in the commercial gel-cap formulation in Table 1.
Treatment IV consisted of three consecutive bolus injections of Aloxi 25 mg.
Pharmacokinetic parameters are reported below in Table 7:
Pharmacokinetics are also reported in
A bioequivalence study was undertaken to evaluate single oral doses of two formulations (Formulation A and Formulation B) of palonosetron 0.50 mg. Soft gel capsules in healthy male and female subjects. The study was a two treatments, two periods, two sequences, open label, randomized cross-over study.
Pharmacokinetic results are reported in Table 8.
Pharmacokinetic parameters are also reported in
Throughout this application, various publications are referenced. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which this invention pertains. It will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.
The present application claims priority to U.S. Provisional Application No. 60/854,342, filed Oct. 24, 2006 (expired).
| Number | Date | Country | |
|---|---|---|---|
| 60854342 | Oct 2006 | US |
