Patent Application
20100221445
This invention relates generally to the field of estrogen receptor modulators, and to treatment of conditions associated with low estrogen expression and/or low estrogen receptor expression.
O-desmethylvenlafaxine (ODV), the major metabolite of venlafaxine, selectively blocks the reuptake of serotonin and norepinephrine. Klamerus, K. J. et al., “Introduction of the Composite Parameter to the Pharmacokinetics of Venlafaxine and its Active O-Desmethyl Metabolite”, J. Clin. Pharmacol. 32:716-724 (1992). O-desmethylvenlafaxine, chemically named 1-[2-(dimethylamino)-1-(4-phenol)ethyl]-cyclohexanol, was exemplified as a fumarate salt in U.S. Pat. No. 4,535,186. However, the fumarate salt of O-desmethylvenlafaxine has unsuitable physicochemical and permeability characteristics. O-desmethylvenlafaxine is also exemplified as a free base in International Patent Publication No. WO 00/32555.
The succinate form of ODV has been described [U.S. Pat. No. 6,673,838]. The succinate monohydrate form of ODV has been incorporated into an extended release hydro-gel tablet, which reduces adverse effects such as nausea, vomiting, diarrhea, and abdominal pain. Formulations describing the use of hydroxypropyl methylcellulose (HPMC) as the hydrogel matrix have been described [International Patent Publication No. WO 02/064543 A2].
Bazedoxifene acetate (1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-2-(4-hydroxy-phenyl)-3-methyl-1H-indol-5-ol acetic acid), having the chemical formula shown below:
belongs to the class of drugs typically referred to as selective estrogen receptor modulators (SERMs). Consistent with its classification, bazedoxifene demonstrates affinity for estrogen receptors (ER) but shows tissue selective estrogenic effects. For example, bazedoxifene acetate demonstrates little or no stimulation of uterine response in preclinical models of uterine stimulation. Conversely, bazedoxifene acetate demonstrates an estrogen agonist-like effect in preventing bone loss and reducing cholesterol in an ovariectomized rat model of osteopenia. In an MCF-7 cell line (human breast cancer cell line), bazedoxifene acetate behaves as an estrogen antagonist. These data demonstrate that bazedoxifene acetate is estrogenic on bone and cardiovascular lipid parameters and antiestrogenic on uterine and mammary tissue and thus has the potential for treating a number of different disease or disease-like states wherein the estrogen receptor is involved.
U.S. Pat. Nos. 5,998,402 and 6,479,535 report the preparation of bazedoxifene acetate. The synthetic preparation of bazedoxifene acetate has also appeared in the general literature. See, for example, Miller, et al., J. Med. Chem., 2001, 44, 1654-1657. Further description of the drug's biological activity has appeared in the general literature as well (e.g., Miller, et al., Drugs of the Future, 2002, 27(2), 117-121). Formulations of bazedoxifene acetate are also reported in US Patent Application Publication No. 2002/0031548 A1.
What are needed are improved methods of treating conditions associated with low estrogen expression and/or low estrogen receptor expression.
In one aspect, the invention provides a combination product containing, as active compounds, O-desmethylvenlafaxine or a pharmaceutically acceptable salt thereof and bazedoxifene or a pharmaceutically acceptable salt thereof.
In another aspect, the invention provides a multi-layer tablet or capsule in which each active compound is found in a separate layer. In one embodiment, one or both layers is a compressed granulation. In another embodiment, one of the layers is a solid dispersion blend. In still another embodiment, the invention provides a capsule containing a multiparticulate and a granulation. In a further embodiment, the core is composed of one active compound and another active compound is provided in a coating layer.
In another aspect, the invention provides a method of treating a subject by administering a composition of the invention.
Still other aspects and advantages of the invention will be apparent from the following detailed description of the invention.
The present invention provides combination products useful for treating disease states or syndromes associated with an estrogen deficiency or an excess of estrogen, as well as in the preparation of medicaments useful therefor. The compositions of the invention are also useful in methods of treatment for diseases or disorders which result from proliferation or abnormal development, actions or growth of endometrial or endometrial-like tissues, as well as in the preparation of medicaments useful therefor.
The combination of the invention utilized as active ingredients, at a minimum, O-desmethylvenlafaxine or a pharmaceutically acceptable salt thereof and bazedoxifene or a pharmaceutically acceptable salt thereof. In one embodiment, the active ingredients are formulated into a single unit dose combination product, e.g., a tablet, capsule, or caplet.
As used herein, O-desmethylvenlafaxine or ODV refers to 1-[2-(dimethylamino)-1-(4-phenol)ethyl]-cyclohexanol. Several pharmaceutically acceptable salts thereof have been described, including, e.g., the fumarate salt thereof [U.S. Pat. No. 4,535,186], the succinate salt form of ODV [U.S. Pat. No. 6,673,838], among others. ODV is also exemplified as a free base in International Patent Publication No. WO 00/32555.
In one embodiment, one of skill in the art can substitute venlafaxine, derivatives and salts thereof, for the ODV described in the examples herein. The succinate salt of ODV (DVS or desvenlafaxine succinate) can be prepared as described in U.S. Pat. No. 6,673,838. The formate salt of ODV (DVF), described in US Patent Application Publication No. US 2003/0236309, can be prepared using similar techniques by substitution of the appropriate salt. Other suitable ODV salts and methods of preparing same can be readily determined by one of skill in the art.
As used herein, bazedoxifene acetate refers to 1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-2-(4-hydroxy-phenyl)-3-methyl-1H-indol-5-ol acetic acid. U.S. Pat. Nos. 5,998,402 and 6,479,535 report the preparation of bazedoxifene and salts thereof. The synthetic preparation of bazedoxifene acetate (BZA) has also appeared in the general literature. See, for example, Miller, et al., J. Med. Chem., 2001, 44, 1654-1657. Alternatively, one of skill in the art can substitute other salts of bazedoxifene for the BZA described in the examples herein.
Still other pharmaceutically acceptable salts of ODV and/or bazedoxifene can be utilized in the combination of the invention. The terms “pharmaceutically acceptable salts” and “pharmaceutically acceptable salt” refer to salts derived from organic and inorganic acids such as, for example, acetic, lactic, citric, cinnamic, tartaric, succinic, fumaric, maleic, malonic, mandelic, malic, oxalic, propionic, hydrochloric, hydrobromic, phosphoric, nitric, sulfuric, glycolic, pyruvic, methanesulfonic, ethanesulfonic, toluenesulfonic, salicylic, benzoic, and similarly known acceptable acids.
In one aspect, the invention provides a product containing the two active ingredients. In one embodiment, the product is designed to contain bazedoxifene in an immediate release formulation and O-desmethylvenlafaxine in a slow release formulation. However, the invention is not so limited.
These two active ingredients may be formulated separately, but in the same form, e.g., each may be in a granulation. Alternatively, the product may contain the active compounds in different forms, e.g., a granulation and a multiparticulate, a granulation and a solid dispersion blend, a multiparticulate and a solid dispersion blend, or in other forms as may be desired.
In one embodiment, the tablet is a multi-layer tablet, in which the active components are contained in separate layers. In one embodiment, the tablet contains two layers with active compounds. In another aspect, the invention provides a capsule. Such a capsule may be filled with a tablet as described herein, or contain the two actives in different formulations. In one embodiment, a capsule according to the invention contains desvenlafaxine succinate multiparticulates and bazedoxifene or a pharmaceutically acceptable salt thereof. In a further embodiment, the bazedoxifene or pharmaceutical salt thereof is in the form of a solid dispersion. In another embodiment, the bazedoxifene or pharmaceutically acceptable salt thereof is in the form of a granulation. In yet another embodiment, the bazedoxifene is a coating applied to the multiparticulates. In a further embodiment, a pharmaceutically acceptable salt of bazedoxifene is used. In another embodiment, a multiparticulate contains desvenlafaxine succinate and microcrystalline cellulose.
In a further embodiment, the bazedoxifene is provided as a coating over a DVS layer, DVS tablet, or DVS multiparticulate core. In the examples below, a bazedoxifene film coat over a DVS tablet core and a bazedoxifene, sugar-based, coat over a DVS tablet core are illustrated.
In one embodiment, a tablet according to the invention is prepared having a first layer containing desvenlafaxine succinate, hypomellose, microcrystalline cellulose, talc, and magnesium stearate, and a second layer containing bazedoxifene or a pharmaceutically acceptable salt thereof. In one embodiment, the ODV formulation of the first layer contains hypomellose, microcrystalline cellulose, and talc. In a further embodiment, the ODV layer is composed of:
In one embodiment, the DVS is about 50 wt % and the hypomellose is about 40 wt % of that layer. Suitably, this mixture can be prepared in the form of a granulation or another suitable form.
In another embodiment, the second contains bazedoxifene acetate, lactose, microcrystalline cellulose, and starch. Additional BZA formulations are described below.
Regardless of the form of the combination product, the product desirably contains as a unit dose, about 10 mg to 500 mg O-desmethylvenlafaxine (ODV) or a salt thereof, wherein the dose amount is calculated based on the amount of O-desmethylvenlafaxine free base, and about 5 mg to 100 mg bazedoxifene or a pharmaceutically acceptable salt thereof, calculated based on the amount of bazedoxifene. In one embodiment, the product contains a succinate salt, i.e., termed herein desvenlafaxine succinate (DVS). In another embodiment, the product contains bazedoxifene acetate (BZA). In yet another embodiment, the ODV salt is DVS and the bazedoxifene is BZA. However, the invention is not so limited.
In other embodiments, the unit dose is in the range of 25 mg to 250 mg ODV, or 50 mg to 200 mg ODV, or about 150 mg ODV, as calculated based on the amount of O-desmethylvenlafaxine free base. In these and other embodiments, the unit dose of bazedoxifene is in the range of 10 mg to 75 mg bazedoxifene, 20 mg to 50 mg bazedoxifene, about 25 mg to about 40 mg bazedoxifene, or about 20 mg bazedoxifene, calculated on the basis of free bazedoxifene.
Suitably, the ODV salt is admixed with one or more components selected from the group including, diluents, binders, fillers, glidants, anti-adherents, and adjuvants. The binder may be selected from among known binders, including, e.g., cellulose, and povidone, among others. In one embodiment, the binder is selected from among microcrystalline cellulose, crospovidone, and mixtures thereof.
Suitable pH adjusters include, e.g., sodium carbonate, sodium bicarbonate, potassium carbonate, lithium carbonate, among others. Still other suitable components will be readily apparent to one of skill in the art.
In one embodiment, the ODV or salt thereof is in a formulation which contains rate-controlling components. Typically, such rate controlling components are rate controlling polymers selected from among hydrophilic polymers and inert plasticized polymers. Suitable rate controlling hydrophilic polymers include, without limitation, polyvinyl alcohol (PVA), hypomellose and mixtures thereof. Examples of suitable insoluble or inert “plastic” polymers include, without limitation, one or more polymethacrylates Eudragit® polymer). Other suitable rate-controlling polymer materials include, e.g., hydroxyalkyl celluloses, poly(ethylene) oxides, alkyl celluloses, carboxymethyl celluloses, hydrophilic cellulose derivatives, and polyethylene glycol.
In one embodiment, an ODV multiparticulate can be prepared. See, e.g., US Patent Application Publication No. US 2005/0175698 A1 (published Aug. 11, 2005), entitled, “Multiparticulate O-Desmethylvenlafaxine Salts and Uses Thereof”. In a further embodiment, when the multiparticulate ODV is a spheroid, bead or pellet, the multiparticulate is in the range of about 0.6 mm to about 1 mm in size. However, the multiparticulate may vary in size, without departing from the present invention.
The multiparticulate ODV of the invention are composed, at a minimum, of a core composed of DVS, DVF or a combination thereof, and one or more diluents, binders, fillers, glidants, anti-adherents, a pH adjuster and/or an adjuvant.
Suitably, the total amount of diluent, binders, fillers, glidants, anti-adherents, and adjuvants present in the core is an amount of about 30% w/w to about 97% w/w of the multiparticulate core. For example, when present, a binder, diluent and/or filler can each be present in an amount of about 15% w/w to about 80% w/w, or about 20% w/w to about 70% w/w, or about 25% w/w to about 45% w/w, or about 30% w/w to about 42% w/w of the uncoated dosage form. The total amount of a pH adjuster in the formulation can range from about 0.1% w/w to about 10% w/w of the core, or about 1% w/w to about 8% w/w, or about 3% w/w to about 7% w/w. However, these percentages can be adjusted as needed or desired by one of skill in the art.
The binder may be selected from among known binders, including, e.g., cellulose, and povidone, among others. In one embodiment, the binder is selected from among microcrystalline cellulose, crospovidone, and mixtures thereof.
Suitable pH adjusters include, e.g., sodium carbonate, sodium bicarbonate, potassium carbonate, lithium carbonate, among others. Still other suitable components will be readily apparent to one of skill in the art.
In one embodiment, the DVS and/or DVF is in a sustained release formulation which contains rate-controlling components. In a further embodiment, such rate controlling components are rate controlling polymers selected from among hydrophilic polymers and inert plasticized polymers. Suitable rate controlling hydrophilic polymers include, without limitation, polyvinyl alcohol (PVA), hypomellose and mixtures thereof. Examples of suitable insoluble or inert “plastic” polymers include, without limitation, one or more polymethacrylates Eudragit® polymer). Other suitable rate-controlling polymer materials include, e.g., hydroxyalkyl celluloses, poly(ethylene) oxides, alkyl celluloses, carboxymethyl celluloses, hydrophilic cellulose derivatives, and polyethylene glycol.
In one embodiment, an ODV multiparticulate of the invention contains about 5% w/w to about 75% w/w microcrystalline cellulose (MCC), about 10% w/w to about 70% w/w MCC, about 20% w/w to about 60% w/w, or about 30% w/w to about 50% w/w, based on the weight of the uncoated multiparticulate. In one desirable embodiment, the ODV multiparticulate core contains about 70 wt % to about 30 wt % based on the uncoated multiparticulate.
In one embodiment, the multiparticulate DVS or DVF-containing core is uncoated. The multiparticulates can be placed into a suitable capsule shell or compressed into tablets, using techniques know to those of skill in the art. Suitably, the resulting capsule shell or compressed tablets contain 10 mg to 400 mg of ODV.
In other embodiments, the multiparticulate ODV contain one or more coatings over the core. In still other embodiments, the multiparticulate consists of a pellet core and non-functional seal coating and a functional second coating.
In one embodiment, an initial seal coat can be applied directly to the core. Although the components of this seal coat can be modified by one of skill in the art, the seal coat may be selected from among suitable polymers such as hydroxypropyl methylcellulose (HPMC), ethylcellulose, polyvinyl alcohol, and combinations thereof, optionally containing plasticizers and other desirable components. In a further embodiment, the seal coat contains HPMC. In one embodiment, a seal coat is applied as a HPMC solution at a concentration of about 3% w/w to about 25% w/w, or about 5% w/w to about 7.5% w/w. Upon drying, under suitable conditions, the initial seal coat is in the range of about 1% w/w to about 3% w/w, or about 2% w/w, of the uncoated multiparticulate. In another embodiment, a commercially available seal coat containing HPMC, among other inert components, is utilized. One such commercially available seal coat is Opadry® Clear (Colorcon, Inc.).
In one embodiment, the multiparticulates can contain a further coating layer over the initial seal coat, if present, or directly to the uncoated multiparticulate ODV core, to provide a delay release formulation. These formulations may also lower the incidence of the side effects, including nausea, emesis, and irritable bowel syndrome. Without wishing to be bound by theory, it is believed that these side-effects are avoided by-passing release in the upper GI tract and providing release in the lower GI tract.
An enteric coat (rate-controlling film) may be applied to the multiparticulates and may include, but is not limited to polymethacrylates, hypomellose, ethylcellulose, or a combination thereof. The modified release multiparticulate formulation can contain from about 3% w/w to about 70% w/w of DVS, DVF, or a combination thereof, and from about 5% w/w to about 75% w/w microcrystalline cellulose, based on the weight of an uncoated multiparticulate.
In one embodiment, the enteric coat contains a product which is a copolymer of methacrylic acid and methacrylates, such as the commercially available Eudragit® L 30 K55 (Röhm GmbH & Co. KG). In a further embodiment, the enteric coat is applied such that it coats the multiparticulate in an amount of about 15 to about 45% w/w, about 20% w/w to about 30% w/w, or about 25% w/w to about 30% w/w of the uncoated or initially-coated multiparticulate. In one embodiment, the enteric coat is composed of a Eudragit® L30D-55 copolymer (Röhm GmbH & Co. KG), talc, triethyl citrate, and water. In still another embodiment, the enteric coating contains about 30% w/w of a 30 wt % dispersion of Eudragit® L 30 D55 coating; about 15% w/w talc, about 3% triethyl citrate; a pH adjuster such as sodium hydroxide; and water.
In another embodiment, the enteric coat contains an ethylcellulose-based product, such as the commercially available Surelease® aqueous ethylcellulose dispersion (25% solids) product (Colorcon, Inc.). In one embodiment, a solution of Surelease® dispersion of about 3% w/w to about 25% w/w, or about 3% to about 7%, or about 5% w/w, is applied to the multiparticulate. Upon drying under suitable conditions, the enteric coat is in the range of about 2% to about 5%, or about 3% to about 4% w/w of the uncoated or initially-coated multiparticulate.
Other formulations containing an ODV salt, including DVS, can be determined by one of skill in the art.
In another aspect, a composition of the invention contains as an active ingredient, bazedoxifene or a pharmaceutically acceptable salt thereof, containing 5 mg to 100 mg bazedoxifene. The bazedoxifene formulation can form a separate layer from the ODV salt in a tablet, or other combination product.
In one embodiment, the bazedoxifene formulation contains bazedoxifene acetate, lactose, microcrystalline cellulose, and starch.
In another embodiment, the bazedoxifene formulation contains:
In yet another embodiment, the bazedoxifene formulation contains:
These formulations are particularly well suited for the preparation of a granulation. In one embodiment, the product contains a 40 mg granulation of bazedoxifene acetate.
In one embodiment, the product contains a layer having a solid dispersion blend having an amount of bazedoxifene or a salt thereof equivalent to 5 mg to 100 mg, about 10 mg to 50 mg, about 25 mg to about 40 mg bazedoxifene. In another embodiment, the solid dispersion blend contains about 20 mg bazedoxifene or a salt thereof.
In one embodiment, the compositions of the invention contain BZA dispersed in a dispersing agent. In another embodiment, the weight ratio of BZA to dispersing agent is about 1:99 to about 99:1. In yet another embodiment, the weight ratio of BZA to dispersing agent is about 1:99 to about 75:25 or about 1:99 to about 60:40. In a further embodiment, the weight ratio of BZA to dispersing agent is about 1:99 to about 15:85; about 1:99 to about 10:90; or about 1:99 to about 5:95. In another embodiment, the weight ratio of BZA to dispersing agent is about 5:95. In still another embodiment, the weight ratio of BZA to dispersing agent is about 25:75 to about 75:25, about 40:60 to about 60:40, or about 1:1. In another embodiment, the weight ratio of BZA to dispersing agent is about 1:1.
The “dispersing agent,” as used herein, refers to any substance or mixture of substances that acts as a suspending medium for particles of solid bazedoxifene acetate. The dispersing agent is typically composed of a pharmaceutically acceptable substance that does not substantially interfere with the pharmaceutical action of BZA. The phrase “pharmaceutically acceptable” is employed herein to refer to those substances which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. In some embodiments, the dispersing agent is a solid at room temperature (e.g., about 22° C.). In further embodiments, the dispersing agent melts at a temperature between about 30° C. and 100° C. In further embodiments, the dispersing agent is soluble in an organic solvent.
Non-limiting examples of suitable dispersing agents include polymers such as celluloses (e.g., carboxymethylcelluloses, methylcelluloses, hydroxypropylcelluloses, hydroxypropylmethylcelluloses); hyaluronates; alginates; polysaccharides, heteropolysaccharides (pectins); poloxamers; poloxamines; ethylene vinyl acetates; polyethylene glycols; dextrans; polyvinylpyrrolidones; chitosans; polyvinylalcohols; propylene glycols; polyvinylacetates; phosphatidylcholines (lecithins); miglyols; polylactic acid; polyhydroxybutyric acid; mixtures of two or more thereof, copolymers thereof, derivatives thereof, and the like. Further examplary dispersing agents include copolymer systems such as polyethylene glycol-polylactic acid (PEG-PLA), polyethylene glycol-polyhydroxybutyric acid (PEG-PHB), polyvinylpyrrolidone-polyvinylalcohol (PVP-PVA), and derivatized copolymers such as copolymers of N-vinyl purine (or pyrimidine) derivatives and N-vinylpyrrolidone. In one embodiment, the dispersing agent contains polyvinylpyrrolidone (PVP) or a derivative thereof. PVP is a polyimide that forms complexes with a wide variety of substances and is considered to be chemically and physiologically inert. Examples of suitable PVPs include polyvinylpyrrolidone(s) having an average molecular weight from about 10,000 to about 50,000. In one embodiment, the polyvinylpyrrolidone has an average molecular weight of about 10,000 to about 20,000. In another embodiment, the polyvinylpyrrolidone has a molecular weight of about 15,000 to about 20,000. In yet another embodiment, multiple polyvinylpyrrolidones are utilized in the dispersing agent. In still another embodiment, polyvinylpyrrolidones of differing weights may be utilized. An example suitable PVP is PVP K-17 (PLASDONE povidone, ISP Technologies, Ltd.). In one embodiment, the dispersing agent consists essentially of PVP or derivative thereof.
In one embodiment, the dispersing agent contains a block co-polymer of ethylene and propylene glycol, often referred to as a Poloxamer. Some suitable exemplary Poloxamers include Poloxamer 188 (LUTROL F 68, BASF), Poloxamer 407 (LUTROL F 127, BASF), and the like. In a further embodiment, the dispersing agent is Poloxamer 188.
In one embodiment, the dispersing agent contains a polyethylene glycol (PEG). Suitable PEGs include PEG 200, 300, 400, 600, 1000, 1450, 3350, 4000, 6000, 8000, 10000, 20000, mixtures thereof and the like. In a further embodiment, the dispersing agent is PEG 1450.
The BZA dispersions useful in the invention can be made by any method that results in, for example, a solid dispersion of amorphous BZA. In one embodiment, BZA (in any form, e.g., crystalline, amorphous, etc.) and the dispersing agent are dissolved in a dispersing solvent (together, or separately and then combined) in the weight ratio desired and then the dispersing solvent is removed to yield the desired solid dispersion. The dispersing solvent can be an aqueous solvent or organic solvent. Suitable organic solvents include alcohols, ethers, hydrocarbons, halogenated hydrocarbons, nitriles, mixtures thereof, and the like. In another embodiment, the organic solvent is a volatile solvent such as methanol, ethanol, isopropanol, diethyl ether, pentane, hexane, benzene, dichloromethane, acetonitrile, mixtures thereof and the like. In a further embodiment, the organic solvent is an alcohol such as methanol, ethanol, n-propanol, ispropanol, mixtures thereof and the like. In some embodiments, the organic solvent is ethanol.
In one embodiment, BZA and dispersing agent are combined in the desired weight ratio when either or both the BZA and dispersing agent is (are) in liquid form (e.g., a melt), and then the liquid mixture is solidified to form the desired solid dispersion. In a further embodiment, the BZA and dispersing agent are combined when at least one of the BZA and dispersing agent is melted. The resulting mixture is then solidified by cooling to a temperature sufficient to solidify the mixture. In a further embodiment, the mixture is cooled to about 25° C. or below. In another embodiment, BZA is combined with melted dispersing agent and the resulting mixture cooled to a temperature below the melting point of the mixture to form the solid dispersion. In one embodiment, the dispersing agent is heated to a temperature between about 30 and 200° C., between about 30 and 150° C., or between about 30 and 100° C., which is a temperature that is at or above the melting point of the dispersing agent. In a further embodiment, the dispersing agent is heated to a temperature above about 30° C., above about 40° C., above about 50° C., above about 60° C., above about 70° C., above about 80° C., or above about 90° C. These and other methods are routine techniques suitable for the preparation of the BZA dispersions of the invention.
In one embodiment, the solid dispersions useful in the invention are characterized by an equilibrium solubility in 0.0005 M acetic acid at a temperature of about 20 to about 26° C. that is greater than that for crystalline or microcrystalline bazedoxifene acetate. In a further embodiment, the solid dispersions of the invention are characterized by an equilibrium solubility in 0.0005 M acetic acid at a temperature of about 20 to about 26° C. that is at least about 8, at least about 10, at least about 12, at least about 14, at least about 16, or at least about 19 mg/mL. Equilibrium solubility can be measured by routine methods in the art.
In one embodiment, the solid dispersions useful in the invention are characterized such that a dosage form comprising about 10 mg total of bazedoxifene acetate in a solid dispersion is characterized by an AUC0-24 greater than about 140, greater than about 150, greater than about 160, greater than about 170, or greater than about 180 ng·hr/mL when orally administered to mammal. In a further embodiment, the solid dispersions useful in the invention are characterized such that a dosage form comprising about 10 mg total of bazedoxifene acetate in a solid dispersion is characterized by: a) an AUC0-24 of about 140 to about 250 ng·hr/mL; b) a Cmax of about 12 to about 30 ng/mL, and c) a tmax of about 1.0 to about 3.5 hr; when orally administered to mammal. Methods for measuring the pharmacokinetic parameters AUC0-24 (area under curve for 24 hours), Cmax, and tmax are well known and described in the art.
Additional details on preparation and characterized of the solid BZA dispersion useful in the present invention are described in US Patent Publication No. US 2005/0227966 A1, published Oct. 13, 2005.
In one embodiment, a product of the invention contains a layer of a solid dispersion blend of BZA having the formulation:
In another embodiment, the formulation contains about 1 wt % magnesium stearate, or less. Still other bazedoxifene granulations or solid dispersion blends, or other formulations can be utilized.
In one embodiment, the bazedoxifene is provided in the form of a coat or a layer applied over a DVS core (e.g., a layer, a multiparticulate, or a tablet). The coat may be applied directly over the DVS core or there may be intermediate layers.
In one embodiment, the bazedoxifene coat provides an amount of 4-6 wt % bazedoxifene acetate, and preferably about 5 wt % bazedoxifene per dosage unit. In another embodiment, bazedoxifene is provided in a coating layer in an amount of about 20 mg per tablet.
Bazedoxifene can be mixed into a suitable coating suspension and applied using conventional spray methods. In one embodiment, BZA is mixed into a hypomellose-based clear coat system (e.g., Opadry® clear coat) at a ratio of about 1:2 BZA to Opadry® clear coat (based on weight). In another embodiment, BZA is mixed into a sugar based overcoat. In still another embodiment, BZA is mixed with a sugar-based coating suspension containing sucrose, hypomellose, sucrose palmitate and ascorbic acid.
Still other suitable coating solutions will be apparent to one of skill in the art.
In one aspect, the present invention provides a method of preparing a combination product from separately formulated ODV or salt thereof and a bazedoxifene combination product.
In one embodiment, the active components are prepared in the form of a multi-layer tablet or tablet-in-capsule. For example, a O-desmethylvenlafaxine is mixed with suitable excipients to form a first granulation and a bazedoxifene is mixed with suitable excipients to form a second granulation. In one embodiment, one or both granulations are formed using a roller compactor. In another embodiment, one or both granulations are formed using a high shear granulator. However, other methods known to those of skill in the art, including, e.g., a low shear granulator, a blender, etc., can be utilized to prepare suitable granulations. The first granulation and the second granulation are then compressed using conventional methods to form a bi-layer tablet. This tablet may be provided with additional layers, optionally, containing additional layers with active components, or other layers as may be desired for enteric coating, seal coating, separation between layers, or the like. In one embodiment, the tablet core contains only one of the active components and the other active component is provided in a coating layer.
In another embodiment, a final seal coat is applied over the tablet. Suitably, this final seal coat is composed of hydroxypropylmethylcellulose (HPMC) and water, upon drying, is less than about 1 wt % of the total, coated tablet. In a further embodiment, talc is utilized as a final step prior to filling the multi-layer tablets into a suitable packaging unit.
Alternatively or additional, the tablet may be loaded into a capsule.
In another aspect, the invention provides a capsule containing the separately formulated active components in different forms. For example, the capsule may contain a granulation of one active and a multiparticulate of the other active; a multiparticulate of one active and a solid dispersion of the other active; a granulation of one active and a solid dispersion of the other active; a core containing one active compound with the other active components in a coating layer. Such capsules are produced using techniques known to those of skill in the art.
Still other suitable forms of the combination of the invention will be readily apparent to one of skill in the art given the information provided herein. For example, in addition to providing dosing units suitable for oral administration such as tablets, capsules and caplets, the invention provides dosing units suitable for parenteral, transdermal, or mucosal administration.
Also encompassed by the invention are pharmaceutical packs and kits comprising a container, such as a foil package or other suitable container, having a formulation of the invention in unit dosage form.
The compositions and methods of the invention are useful for treating, or for the preparation of medicaments useful in the treatment of, many maladies which result from estrogen effects and estrogen excess or deficiency (e.g., low circulating levels of estrogen) including osteoporosis, prostatic hypertrophy, male pattern baldness, vaginal and skin atrophy, acne, dysfunctional uterine bleeding, endometrial polyps, benign breast disease, uterine leiomyomas, adenomyosis, ovarian cancer, infertility, breast cancer, endometriosis, endometrial cancer, polycystic ovary syndrome, cardiovascular disease, contraception, Alzheimer's disease, cognitive decline and other CNS disorders, as well as certain cancers including melanoma, prostrate cancer, cancers of the colon, CNS cancers, among others. Additionally, the compositions and methods can be used for contraception in pre-menopausal women, as well as hormone replacement therapy in post-menopausal women (such as for treating vasomotor disturbances such as hot flush) or in other estrogen deficiency states where estrogen supplementation would be beneficial. It can also be used in disease states where amenorrhea is advantageous, such as leukemia, endometrial ablations, chronic renal or hepatic disease or coagulation diseases or disorders.
The compositions and methods of the invention can also be used for inhibition of, or for the preparation of medicaments useful in the inhibition of, bone loss, which can result from an imbalance in a subject's formation of new bone tissues and the resorption of older tissues, leading to a net loss of bone. Such bone depletion results in a range of individuals, particularly in post-menopausal women, women who have undergone bilateral oophorectomy, those receiving or who have received extended corticosteroid therapies, those experiencing gonadal dysgenesis, and those suffering from Cushing's syndrome. Special needs for bone (including teeth and oral bone) and bone replacement can also be addressed using the present solid dispersion in individuals with bone fractures, defective bone structures, and those receiving bone-related surgeries and/or the implantation of prosthesis. In addition to the problems described above, the compositions and methods of the invention can be used in treatments for, or in the preparation of medicaments useful in treating, osteoarthritis, hypocalcemia, hypercalcemia, Paget's disease, osteomalacia, osteohalisteresis, multiple myeloma and other forms of cancer having deleterious effects on bone tissues.
In addition, the combination of the invention is useful in alleviating the symptoms of depression, fibromyalgia, anxiety, stress urinary incontinence (S.U.I.), irritable bowel syndrome (I.B.S.), neuropathic pain, and other post meno-pausal symptoms including, e.g., host flushes, osteoporosis, vaginal atrophy, etc.
Methods of treating the diseases and syndromes listed herein are understood to involve administering to a subject in need of such treatment a therapeutically effective amount of the solid dispersion of the invention, or composition containing the same. As used herein, the term “treating” in reference to a disease is meant to refer to preventing, inhibiting and/or ameliorating the disease.
As used herein, the term “subject”, “individual” or “patient,” used interchangeably, refers to any mammals, preferably mice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep, horses, or primates, and most preferably humans.
As used herein, the phrase “therapeutically effective amount” refers to the amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue, system, or subject that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes one or more of the following disease prevention, i.e., a subject who does not yet experience or display the pathology or symptomatology sufficient to definitively diagnose the disease; disease inhibition, i.e., arresting or slowing further development of the pathology and/or symptomatology); and ameliorating the disease.
In one embodiment, the dosage of venlafaxine is about 75 mg to about 350 mg/day or about 75 mg to about 225 mg/day. In a further embodiment, the dosage of venlafaxine is about 75 mg to about 150 mg/day. When a DVS multiparticulate is utilized, the amount of the DVS multiparticulate will correspond to the dosage ranges for the venlafaxine free base. These may vary from patient to patient depending upon a patient's response rate, but generally will be at least 6:1 ODV salt to venlafaxine. Venlafaxine or another active agent delivered in a regimen with the multiparticulate of the invention may be formulated together with the multiparticulate of the invention, or delivered separately.
Formulations containing the present solid dispersions can be administered in daily doses ranging from 0.1 mg to 1000 mg of bazedoxifene acetate to a subject in need. In one embodiment, dose ranges vary from about 10 mg/day to about 600 mg/day, or from about 10 mg/day to about 60 mg/day. The dosing can be either in a single dose or two or more divided doses per day.
Any suitable route of administration can be employed for providing the patient with an effective amount of the combination product of the invention. For example, oral, mucosal (e.g., nasal, sublingual, buccal, rectal or vaginal), parental (e.g., intravenous or intramuscular), transdermal, and subcutaneous routes can be employed. In one embodiment, the route of administration is oral, transdermal, or mucosal.
The active compounds described herein are typically combined with a pharmaceutical carrier or excipient (e.g., pharmaceutically acceptable carriers and excipients) according to conventional pharmaceutical compounding technique to form a pharmaceutical composition or dosage form. Suitable pharmaceutically acceptable carriers and excipients include, but are not limited to, those described in Remington's, The Science and Practice of Pharmacy, (Gennaro, A. R., ed., 19th edition, 1995, Mack Pub. Co.). The phrase “pharmaceutically acceptable” refers to additives or compositions that are physiologically tolerable and do not typically produce an allergic or similar untoward reaction, such as gastric upset, dizziness and the like, when administered to an animal, such as a mammal (e.g., a human).
Oral solid pharmaceutical compositions may include, but are not limited to, starches, sugars, microcrystalline cellulose, diluents, granulating agents, lubricants, binders and disintegrating agents.
In one aspect, the invention provides a method for preventing or minimizing the formation of isatin oximes, comprising preparing an isatin from an isonitrosoacetanilide in the presence of a decoy agent comprising a carbonyl group. In one embodiment, the method further comprises extracting said isatin in said decoy agent. In another embodiment, the extraction further comprises a solvent. In a further embodiment, the solvent is isopropyl acetate, 2-butantone, 3-pentanone, or methyl isobutyl ketone. In a further embodiment, the isatin is of the structure:
wherein R1 is H, OH, NH2, C1 to C6 alkyl, or substituted C1 to C6 alkyl; R2, R3, R4, and R5 are independently selected from the group consisting of halogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, OR6, N(R7)2, CON(R7)2, SO2N(R7)2, NO2, CN, and C(O)R8; or R2 and R3; R3 and R4; R4 and R5; or R5 and R1 are fused to form a (i) a 3 to 14 membered carbon-based saturated or unsaturated ring or (ii) a 3 to 14 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; R6 is CF3, C1 to C6 alkyl or C1 to C6 substituted alkyl; R7 is H, C1 to C6 alkyl, C1 to C6 substituted alkyl, CF3, C(O)R9, NC(O)R9, or (C1 to C6 alkyl)NC(O)R9; or two of R7 are fused to form a -A-(CH2)n-A- ring; n is 1 to 6; A are independently selected from the group consisting of O, S, and N; R8 is H, OH, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy; and R9 is CF3, C1 to C6 alkyl, substituted C1 to C6 alkyl, NHC(O)CF3, and CH2CH2NHC(O)CF3.
In a further embodiment, R2, R3, R4, and R5 are independently selected from the group consisting of halogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, OR6, N(R7)2, CON(R7)2, SO2N(R7)2, and C(O)R8; or R2 and R3; R3 and R4; R4 and R5; or R5 and R1 are fused to form a (i) a 3 to 9 membered carbon-based saturated or unsaturated ring or (ii) a 3 to 9 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; R6 is C1 to C6 alkyl or C1 to C6 substituted alkyl; and R7 is H, C1 to C6 alkyl, C1 to C6 substituted alkyl, or CF3. In a further embodiment, R2 and R3; R3 and R4; or R4 and R5 are fused to form —OCH2CH2O—.
In one embodiment, the isatin is 7-fluoroisatin. In a further embodiment, the isatin oxime is of the structure:
wherein R1-R5 is H, OH, NH2, C1 to C6 alkyl, or substituted C1 to C6 alkyl; R2, R3, R4, and R5 are independently selected from the group consisting of halogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, OR6, N(R7)2, CON(R7)2, SO2N(R7)2, and C(O)R8; or R2 and R3; R3 and R4; R4 and R5; or R5 and R1 are fused to form a (i) a 3 to 14 membered carbon-based saturated or unsaturated ring or (ii) a 3 to 14 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; R6 is C1 to C6 alkyl or C1 to C6 substituted alkyl; R7 is H, C1 to C6 alkyl, C1 to C6 substituted alkyl, or CF3; and R8 is H, OH, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy.
In one embodiment, the decoy agent is of the structure:
wherein X and Z are, independently, H, C1 to C6 alkyl, substituted C1 to C6 alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, C1 to C12 alkyl(O)R2, substituted C1 to C12 alkyl(O)R2, C3 to C8 cycloalkyl C(O)R2, substituted C3 to C8 cycloalkyl C(O)R2, CY3, COOR2, or (C1 to C6)OH; R2 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, aryl, substituted aryl, heteroaryl, or substituted heteroaryl; and Y is halogen.
In a further embodiment the decoy agent is selected from the group consisting of formaldehyde, paraform, formalin, acetaldehyde, propionaldehyde, acetone, 2-butanone, 2-pentanone, 3-pentanone, 4-methyl-2-pentanone, dimethoxyacetaldehyde, benzaldehyde, acetophenone, thiophenecarboxaldehyde, glyoxal, chlorals, mesoxalates, glyoxylates, pyruvates, hexafluoroacetone, diacetyl, glyoxylic acid, a corresponding hydrate, and combinations thereof. In one embodiment, the decoy agent is acetone, chloral hydrate, glyoxal, or ethyl glyoxalate. In another embodiment, the decoy agent is formed during said method. In another embodiment, the decoy agent is formed from a latent decoy agent. In another embodiment, the decoy agent is a reducing sugar. In another embodiment, the reducing sugar is selected from the group consisting of glucose, lactose, and maltose. In another embodiment, the latent decoy agent is an acetal, ketal, ketal thio-derivative, or bisulfite addition compound. In another embodiment, the ketal is trioxane, diethoxymethane, dimethoxymethane, 2,2-dimethoxypropane, 1,1-dimethoxyethane, 1,1,3,3-tetramethoxypropane, diethylacetaldehyde acetal, 1,3-dioxane, 1,3-dioxolane, or (CH3)2C(−OCH2CH2CH2O—).
In yet another embodiment the isonitrosoacetanilide is of the structure:
wherein R1 is H, OH, NH2, C1 to C6 alkyl, or substituted C1 to C6 alkyl; R2, R3, R4, and R5 are independently selected from the group consisting of halogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, OR6, N(R7)2, CON(R7)2, SO2N(R7)2, and C(O)R8; or R2 and R3; R3 and R4; R4 and R5; or R5 and R1 are fused to form a (i) a 3 to 14 membered carbon-based saturated or unsaturated ring or (ii) a 3 to 14 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; R6 is C1 to C6 alkyl or C1 to C6 substituted alkyl; R7 is H, C1 to C6 alkyl, C1 to C6 substituted alkyl, or CF3; and R8 is H, OH, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy. In a further embodiment, the isonitrosoacetanilide is selected from the group consisting of N1-(2-fluorophenyl)-2-hydroxyiminoacetamide; 4-fluoroisonitrosoacetanilide; and 5,6,7,8-napthyl-1-isonitrosoacetanilide; and N1-(2,4-dichlorophenyl)-2-hydroxyiminoacetamide.
In one embodiment, the isatin is formed in the presence of a strong acid. In a further embodiment, the strong acid is selected from the group consisting of sulfuric acid, polyphosphoric acid, methanesulfonic acid, and combinations thereof.
In another aspect, the invention provides a product prepared by the method comprising preparing an isatin from an isonitrosoacetanilide in the presence of a decoy agent comprising a carbonyl group
In another aspect, the invention provides a method for preventing or minimizing the formation of isatin oximes, comprising quenching the reaction for forming an isatin from an isonitrosoacetanilide in the presence of a decoy agent comprising a carbonyl group.
In another aspect, the invention provides a method of preparing 7-fluoroisatin by reacting 2-fluoroisonitrosoacetanilide with a strong acid and quenching said reaction with a decoy agent comprising a carbonyl group.
In another aspect, the invention provides a method for preventing or minimizing the formation of isatin oximes, comprising (i) preparing an isatin from an isonitrosoacetanilide in a first decoy agent comprising a carbonyl group; and (ii) extracting said isatin in a second decoy agent comprising a carbonyl group. In one embodiment, the first and second decoy agents are the same. In another embodiment, the first and second decoy agents are different.
In another aspect, the invention provides, a method for preparing an isatin oxime comprising reacting an isonitrosoacetanilide with a hydroxylamine or salt thereof. In one embodiment, the hydroxylamine salt is selected from the group consisting of hydroxylamine hydrochloride, hydroxylamine sulfate, hydroxylamine phosphate, and hydroxylamine nitrate.
In one aspect, the invention provides a method of preparing 5-(7-fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile, comprising: (a) reacting 2-fluoroaniline, chloral hydrate, and hydroxylamine hydrochloride; (b) reacting the product of step (a) with sulfuric acid in the presence of hexane and a decoy agent; (c) reacting the product of step (b) with hydrazine and glycol; (d) reacting the product of step (c) with 2 equivalents of methylbromide; (e) reacting the product of step (d) with bromine; and (f) reacting the product of step (e) with 5-1,3,6,2]dioxazaborocyan-2-yl-1-methyl-1H-pyrrole-2-carbonitrile.
In one aspect, the invention provides a method of preparing 5-(7-fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile, comprising: (a) reacting 2-fluoroaniline, chloral hydrate, and hydroxylamine hydrochloride; (b) reacting the product of step (a) with sulfuric acid in the presence of hexane; (c) quenching the reaction of step (b) using a decoy agent; (d) reacting the product of step (c) with hydrazine and glycol; (e) reacting the product of step (d) with 2 equivalents of methylbromide; (f) reacting the product of step (e) with bromine; and (g) reacting the product of step (f) with 5-[1,3,6,2]dioxazaborocyan-2-yl-1-methyl-1H-pyrrole-2-carbonitrile.
In one aspect, the invention provides a method of preparing 5-(7-fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile, comprising: (a) reacting 2-fluoroaniline, chloral hydrate, and hydroxylamine hydrochloride; (b) reacting the product of step (a) with sulfuric acid in the presence of hexane; (c) extracting the product of step (b) using a decoy agent; (d) reacting the product of step (c) with hydrazine and glycol; (e) reacting the product of step (d) with 2 equivalents of methylbromide; (f) reacting the product of step (e) with bromine; and (g) reacting the product of step (f) with 5-[1,3,6,2]dioxazaborocyan-2-yl-1-methyl-1H-pyrrole-2-carbonitrile.
The following examples illustrate exemplary dosage forms of the products of the invention, and the use thereof. These examples are not a limitation of the present invention.
A tablet containing two layers having active compounds was prepared according to the following tables.
A. Preparation
The DVS-233 granulation was prepared via dry granulation using an Alexanderwerks roller compactor. The bazedoxifene granulation was prepared using a high shear granulator (Collette Gral) and dried in a fluid bed dryer. Bilayer tablets were compressed using a Carver press with 0.735″×0.325″ capsule shaped tooling.
B. Stability
80 DVS/Bazedoxifene bilayered tablets (150 mg/40 mg respectively) were stored at 25° C./60 relative humidity (RH) and 40° C./75 RH in a 50-mL high density polyethylene (HDPE) closed container for 2 weeks, 1 month and 3 months. The strengths of each active constituents and the dissolution rate in 0.2% Tween 80/10 mM Acetic acid at 37° C. were monitored.
Strength (% Recovery) of BZA and ODV for different treatments is shown in the following table.
Both BZA and ODV are stable in 25/60 and 40/75 for 3 months.
Dissolution of these bilayer tablets also showed that almost complete releases in 24 hours were achieved for both BZA and DVS. Where BZA gave a % release of more than 75% in 45 minutes and more than 93% release in 24 hours. DVS gave a slow release in the first 2 hours but it gave a complete release in 24 hours. Tablets core stay intact in the dissolution vessels after 24 hours and tablets that was treated at 40° C./75 RH for 3 months look more discolored (more faint-yellowish) than tablets of 25° C./60 RH treatments. These tablets were designed as an immediate release for BZA and a slow release for DVS and the dissolution pattern was consistent with this design.
DVS-233 multiparticulates were prepared as described in co-owned US Patent Publication No. US 2005/0175698 A1, published Aug. 11, 2005, for “Multiparticulate O-Desmethylvenlafaxine Salts and Uses Thereof” (Diorio, et al).
A. Desvenlafaxine Succinate Multiparticulates
The multiparticulate consists of a pellet core and non-functional seal coating and a functional second coating. The manufacturing of the multiparticulate core was as follows. The desvenlafaxine succinate (DVS-233) is combined with microcrystalline cellulose and granulated with water in a planetary mixer. Then using the Nica® System the resulting wet mass is extruded through a 1.0 mm screen. The DVS-233 extrudates are then transferred to the spheronizer and spun at approximately 700 rpm until spherical pellets are obtained (2-3 minutes).
The wet pellets are then dried in an Aeromatic Strea fluid bed dryer to a moisture level of 2-5%. The dried pellets are passed through a 18 mesh screen to remove larger oversize pellets. The pellets are now ready for the coating process.
B. Coating
1. Seal Coat
The Aeromatic Strea fluid bed apparatus is fitted with a Wurster column and bottom spray nozzle system. Approximately 200 grams of the dried pellet cores are charged into the unit. The Opadry® seal coat is applied with a inlet temperature of approximately 60° C., a coating solution spray rate of 5-10 grams/minute, atomization pressure of 1-2 bar. The desired product temperature is 38° C.-43° C. After approximately a 2% weight gain of the seal coat is achieved the ethylcellulose coat can be applied.
2. Ethylcellulose Coat
The ethylcellulose is applied in a similar fashion as the seal coat to a weight gain of 3-4%. After the ethylcellulose coat is applied, the pellets are dried for an additional 5-10 minutes. They are removed and screened through an 18 mesh screen to remove agglomerates and oversized particles.
C. DVS-233 Multiparticulates 150 mg/BZA 40 mg Capsules
The coated DVS-233 pellets are encapsulated to achieve a strength of 150 mg of desvenlafaxine. The BZA granulation, as described above, is placed into the same hard gelatin capsule shell.
A. Desvenlafaxine Succinate 150 mg Granulation
B. Bazedoxifene Solid Dispersion Blend
BZA acetate, Solid Dispersion with polyvinylpyrrolidone (PVP) at a ratio of 1:1 was prepared as described in co-owned US Patent Publication No. US 2005/0227966 A1 (published Oct. 13, 2005), entitled “Bazedoxifene Acetate Formulations” (Shah, et al.).
In summary, to a solution of 3.00519 g of PVP K17 in 15 mL of ethanol, was added 3.00671 g of BZA with mixing. Another 60 mL of ethanol was added and the mixture was wormed to 65° C. for 5 minutes to get a clear yellow-brown solution. Solvents were evaporated under reduced pressure at room temperature to dryness. The yellow-brown solid was grinded with mortar and pestle to give yellow-creamy fine powder.
The DVS-233 granulation was prepared via dry granulation using an Alexanderwerks roller compactor. The bazedoxifene solid dispersion blend was prepared by direct blending using a mortar and pestle. Bilayer tablets were compressed using a Carver press with 0.450 inch square shaped tooling.
The coated DVS-233 pellets described in Example 2 above are encapsulated to achieve a strength of 150 mg of desvenlafaxine. The BZA solid dispersion blend as described in Example 3 above, is placed into the same hard gelatin capsule shell.
A. DVS-233 100 mg Sustained Release Tablet Cores
1The DVS-233 potency of this tablet is equivalent to 100 mg desmethylvenlafaxine free base.
B. Bazedoxifene film-coat overcoat process
The Opadry Clear coat system contains hypomellose and is prepared at a concentration of 10% w/w.
The coating suspension is prepared by dissolving the Opadry Clear coat powder in the appropriate amount of water to obtain a solution that contains about 10% dissolved solids. The solution is mixed until a clear solution is obtained. Micronized bazedoxifene acetate is added to the Opadry solution slowly under vigorous mixing until a homogenous suspension is obtained. The Opadry/bazedoxifene suspension is sprayed onto the DVS-233 tablet cores under the following conditions using a Thomas LDCS 1.31 pan.
C. Bazedoxifene, Sugar Based, Overcoat Process
A coating suspension is prepared by dissolving the sucrose, sucrose palmitate, hypomellose, and ascorbic acid in water. Micronized bazedoxifene acetate is added to the sucrose solution slowly under vigorous mixing until a homogenous suspension is obtained. The sucrose/bazedoxifene suspension is sprayed onto the DVS-233 tablet cores under the following conditions using a Thomas LDCS 1.31 pan.
A color and/or clear gloss coat may be applied after the sucrose/bazedoxifene suspension has been applied.
The present invention is not to be limited in scope by the specific embodiments described herein. Various modifications to these embodiments will be obvious to one of skill in the art from the description. Such modifications fall within the scope of the appended claims.
Patents, patent applications, publications, procedures and the like are listed throughout the application. These documents are incorporated by reference herein.
This application is a divisional of U.S. patent application Ser. No. 11/386,420, filed Mar. 22, 2006, now pending, which claims the benefit under 35 USC 119(e) of prior U.S. Provisional Patent Application No. 60/666,902, filed Mar. 31, 2005. These priority applications are hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 60666902 | Mar 2005 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11386420 | Mar 2006 | US |
| Child | 12771350 | US |
