WO2022010437A1 - A tablet comprising apixaban - Google Patents
A tablet comprising apixaban Download PDFInfo
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- WO2022010437A1 WO2022010437A1 PCT/TR2021/050445 TR2021050445W WO2022010437A1 WO 2022010437 A1 WO2022010437 A1 WO 2022010437A1 TR 2021050445 W TR2021050445 W TR 2021050445W WO 2022010437 A1 WO2022010437 A1 WO 2022010437A1
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- Prior art keywords
- sodium
- tablet according
- weight
- apixaban
- mixtures
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- 0 C*(C)N1ICCC*1 Chemical compound C*(C)N1ICCC*1 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
Definitions
- Apixaban is a highly selective, orally bioavailable, and reversible direct inhibitor of free and clot-bound factor Xa.
- Factor Xa catalyzes the conversion of prothrombin to thrombin, the final enzyme in the coagulation cascade that is responsible for fibrin clot formation.
- Apixaban has no direct effect on platelet aggregation, but by inhibiting factor Xa, it indirectly decreases clot formation induced by thrombin.
- apixaban and at least one binder are dissolved in a solvent. So, this formulation overcomes the above problems. In this way, an even higher quality of the formulations can be guaranteed with independent of the physical and chemical parameters of apixaban.
- the main object of the present invention is to eliminate problems and bringing additional advantages to the relevant prior art.
- the more clearly main object of the present invention is to provides a tablet comprising apixaban having desired dissolution profile and desired stability with independent of the physical and chemical parameters of apixaban.
- Another object of the present invention is to provide a tablet having improved content uniformity.
- Another object of the present invention is to provides a process for a tablet comprising apixaban.
- the process is a simple, rapid, cost effective, time-saving and industrially convenient method.
- aqueous solubility is the major problem encountered with formulation development.
- Apixaban has poor solubility in water (0.028 mg/mL at 24 °C) and a relatively low oral bioavailability (about 50% for a single 10 mg dose). It is desirable to provide an oral dosage form for active agents of low water solubility in a pharmaceutically acceptable dose.
- the low solubility problem of apixaban was overcome by dissolving apixaban in a solvent except for water.
- good solubility was achieved independent of the particle size of the apixaban.
- at least one binder is dissolved in the same solvent.
- at least one binder and apixaban matrix are obtained. This matrix has an amorphous structure. Thanks to this process, the desired dissolution profile and stability are provided independent of the initial form of the apixaban.
- the amount of apixaban is between 0.5% and 10.0% by weight in the total formulation. Preferably, it is between 1.0% and 8.0% or between 1 .0% and 5.0% or between 1.0% and 3.0% by weight in the total formulation.
- Suitable binders are selected from the group comprising polyvinylpyrrolidone, sodium carboxymethyl cellulose, crospovidone, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, glucose, natural gums, sucrose, sodium alginate, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, carboxy methyl cellulose, methyl cellulose, gelatin, carrageenan, guar gum, carbomer, polymethacrylates, methacrylate polymers, gelatin, alginate, alginic acid, xanthan gum, hyaluronic acid, pectin, polysaccharides, carbomer, poloxamer, polyacrylamide, polyoxyethylene-alkyl ether, polydextrose, polyethylene oxide or mixtures thereof.
- the amount of fillers is between 50.0% and 95.0% by weight in the total formulation. Preferably, it is between 65.0% and 90.0% or between 72.0% and 88.0% by weight in the total formulation.
- the filler is microcrystalline cellulose or lactose or mixtures thereof.
- the disintegrant is croscarmellose sodium or starch or mixtures thereof.
- Suitable surfactants are selected from the group comprising sodium lauryl sulphate, sodium docusate, glyceryl monooleate, polyethylene alkyl ether, polyoxyethylene sorbitan fatty acid ester, sorbic acid, sorbitan fatty acid ester, polyoxyethylene stearates, polyethylene glycol, sodium benzoate, docusate sodium, alpha tocopherol, ascorbyl palmitate, citric acid, polyethoxylated fatty acid esters, polyoxyethylene hydrogenated castor oil or mixtures thereof.
- the tablet comprises apixaban having a particle size of d(0.9) 90 pm to 99 pm.
- the tablet comprises;
- microcrystalline cellulose • 30.0 - 45.0% by weight of microcrystalline cellulose
- the tablet is obtained by using a wet granulation method therefore, a simple and low-cost production method was employed.
- Example 2 The tablet formulation comprising apixaban
- Process for example 1 or 2 a) Dissolving apixaban in a solvent, b) Adding polyvinylpyrrolidone in the solvent and dissolving polyvinylpyrrolidone and then obtained granulation solution, c) Mixing starch, lactose and microcrystalline cellulose and charging the mixture to fluid bed granulator-dryer, d) Then, coating the mixture with the granulation solution comprising apixaban using spray granulation, e) Adding sodium lauryl sulfate and croscarmellose sodium and then mixing, f) Adding magnesium stearate and then mixing, g) Compressing to form of tablets, h) Coating tablets with coating agents.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
The present invention relates to a tablet comprising apixaban and at least one binder wherein apixaban and at least one binder are dissolved in a solvent. The present invention also relates to a simple, rapid, cost effective, time-saving and industrially convenient process.
Description
A TABLET COMPRISING APIXABAN
Field of the Invention
The present invention relates to a tablet comprising apixaban and at least one binder wherein apixaban and at least one binder are dissolved in a solvent. The present invention also relates to a simple, rapid, cost effective, time-saving and industrially convenient process.
Background of the Invention
Apixaban is a highly selective, orally bioavailable, and reversible direct inhibitor of free and clot-bound factor Xa. Factor Xa catalyzes the conversion of prothrombin to thrombin, the final enzyme in the coagulation cascade that is responsible for fibrin clot formation. Apixaban has no direct effect on platelet aggregation, but by inhibiting factor Xa, it indirectly decreases clot formation induced by thrombin.
The chemical name of apixaban is 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1- yl)phenyl]-4,5,6,7-tetrahydro-1 FI-pyrazolo[3,4-c]pyridine-3-carboxamide and its chemical structure is shown in the Formula 1.
Formula I
Apixaban molecule is disclosed in U.S. Patent No. 6,967,208.
Apixaban, sold under the tradename Eliquis, is an anticoagulant for the treatment of venous thromboembolic events. It is taken orally. It is a direct factor Xa inhibitor and apixaban has poor solubility in water (0.028 mg/mL at 24 °C) and a relatively low oral bioavailability (about 50% for a single 10 mg dose).
Apixaban has poor solubility in water (0.028 mg/ml_ at 24 °C) and a relatively low oral bioavailability (about 50% for a single 10 mg dose).
In prior art, there are many patents which disclose oral pharmaceutical dosage forms comprising apixaban.
Pharmaceutical compositions comprising the poorly soluble active ingredient apixaban are known in the art. In particular, several publications teach preparing pharmaceutical compositions comprising apixaban having a particular particle size, for example, WO 2017/182908 A1 describes compositions prepared by using apixaban of particles d(0.9) about 20 pm.
US 2013/0045245 application discloses a composition with improved dissolution rate by using crystalline apixaban having D90 equal to or less than 89 pm and a method for improving the dissolution rate of apixaban as a water insoluble drug by controlling the particle size distribution.
For the low solubility of apixaban, we have seen work done with many particle sizes of apixaban in the prior art. However, the above described methods for improving the dissolution rate by reducing particle size has a problem that the drug distribution in vivo varies depending on the particle size variation.
There is still a need in the art to provide an improved a tablet of apixaban that exhibits improved dissolution rate and good content uniformity, as a property optionally and preferably independent from a particle size of apixaban that may be used.
In the present invention, apixaban and at least one binder are dissolved in a solvent. So, this formulation overcomes the above problems. In this way, an even higher quality of the formulations can be guaranteed with independent of the physical and chemical parameters of apixaban.
Detailed Description of the Invention
The main object of the present invention is to eliminate problems and bringing additional advantages to the relevant prior art.
The more clearly main object of the present invention is to provides a tablet comprising apixaban having desired dissolution profile and desired stability with independent of the physical and chemical parameters of apixaban.
Another object of the present invention is to provide a tablet having improved content uniformity.
Another object of the present invention is to provides a process for a tablet comprising apixaban. The process is a simple, rapid, cost effective, time-saving and industrially convenient method.
The term “apixaban” as used herein refers to apixaban in the form of free base or in the form of pharmaceutically acceptable salts, crystalline polymorph, solvates, hydrates, esters or in an amorphous form or mixtures thereof.
Low aqueous solubility is the major problem encountered with formulation development. Apixaban has poor solubility in water (0.028 mg/mL at 24 °C) and a relatively low oral bioavailability (about 50% for a single 10 mg dose). It is desirable to provide an oral dosage form for active agents of low water solubility in a pharmaceutically acceptable dose.
According to one embodiment of the present invention, a tablet comprises apixaban, wherein apixaban and at least one binder are dissolved in solvent.
According to one embodiment of the present invention, the low solubility problem of apixaban was overcome by dissolving apixaban in a solvent except for water. Thus, good solubility was achieved independent of the particle size of the apixaban. Also, at least one binder is dissolved in the same solvent. In the later steps of the process, after the solvent is removed, at least one binder and apixaban matrix are obtained. This matrix has an amorphous structure. Thanks to this process, the desired dissolution profile and stability are provided independent of the initial form of the apixaban.
In one embodiment, the weight ratio of at least one binder to apixaban is between 1 :1 and 5:1 , preferably between 1 :1 and 3:1. It has been observed that, this ratio is an important factor for achieving desired dissolution profile. When apixaban and at least one binder are used in these ratios, it is also easier to provide a formulation has improved content uniformity with wet granulation.
According to one embodiment of the present invention, the amount of apixaban is between 0.5% and 10.0% by weight in the total formulation. Preferably, it is between 1.0% and 8.0% or between 1 .0% and 5.0% or between 1.0% and 3.0% by weight in the total formulation.
Suitable binders are selected from the group comprising polyvinylpyrrolidone, sodium carboxymethyl cellulose, crospovidone, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, glucose, natural gums, sucrose, sodium alginate, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, carboxy methyl cellulose, methyl cellulose, gelatin, carrageenan, guar gum, carbomer, polymethacrylates, methacrylate polymers, gelatin, alginate, alginic acid, xanthan gum, hyaluronic acid, pectin, polysaccharides, carbomer, poloxamer, polyacrylamide, polyoxyethylene-alkyl ether, polydextrose, polyethylene oxide or mixtures thereof.
According to one embodiment of the present invention, the amount of binders is between 0.5% and 10.0% by weight in the total formulation. Preferably, it is between 1.0% and 8.0% or between 1 .0% and 5.0% by weight in the total formulation.
According to one embodiment of the present invention, the binder is polyvinylpyrrolidone.
Suitable solvent is selected from the group comprising dichloromethane, isopropyl alcohol, ethanol, methanol, acetonitrile, dimethyl sulfoxide, dimethylformamide, ethyl acetate, acetone or mixtures. Preferably, solvent is dichloromethane.
According to one embodiment of the invention, a tablet further comprises at least one pharmaceutically acceptable excipient which is selected from the group comprising fillers, disintegrants, surfactants, lubricants/glidants, coating agents or mixtures.
Suitable fillers are selected from the group comprising microcrystalline cellulose, lactose, mannitol, spray-dried mannitol, lactose monohydrate, dextrose, sucrose, fructose, maltose, sorbitol, xylitol, inorganic salts, calcium salts, polysaccharides, dicalcium phosphate, sodium chloride, dextrates, lactitol, maltodextrin, sucrose-maltodextrin mixture, trehalose, sodium carbonate, sodium bicarbonate, calcium carbonate or mixtures thereof.
According to one embodiment of the present invention, the amount of fillers is between 50.0% and 95.0% by weight in the total formulation. Preferably, it is between 65.0% and 90.0% or between 72.0% and 88.0% by weight in the total formulation.
According to one embodiment of the present invention, the filler is microcrystalline cellulose or lactose or mixtures thereof.
Suitable disintegrants are selected from the group comprising croscarmellose sodium, starch, crospovidone, low-substituted hydroxypropyl cellulose, sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, carboxymethyl cellulose, docusate sodium, guar gum, low substituted hydroxypropyl cellulose, polyacryline potassium, sodium alginate, corn
starch, sodium starch glycolate, alginic acid, alginates, ion-exchange resins, magnesium aluminium silica, sodium dodesyl sulphate, poloxamer, sodium glycine carbonate or mixtures thereof.
According to one embodiment of the present invention, the amount of disintegrants is between 2.0% and 25.0% by weight in the total formulation. Preferably, it is between 3.0% and 5.0%, between 5.0% and 20.0% or between 10.0% and 20.0% by weight in the total formulation.
According to one embodiment of the present invention, the disintegrant is croscarmellose sodium or starch or mixtures thereof.
Suitable surfactants are selected from the group comprising sodium lauryl sulphate, sodium docusate, glyceryl monooleate, polyethylene alkyl ether, polyoxyethylene sorbitan fatty acid ester, sorbic acid, sorbitan fatty acid ester, polyoxyethylene stearates, polyethylene glycol, sodium benzoate, docusate sodium, alpha tocopherol, ascorbyl palmitate, citric acid, polyethoxylated fatty acid esters, polyoxyethylene hydrogenated castor oil or mixtures thereof.
According to one embodiment of the present invention, the amount of surfactants is between 0.5% and 8.0% by weight in the total formulation. Preferably, it is between 1.0% and 6.0% or between 1.0% and 4.0% by weight in the total formulation.
According to one embodiment of the present invention, the surfactant is sodium lauryl sulphate.
Suitable lubricants/glidants are selected from the group comprising from magnesium stearate, talc, colloidal silicon dioxide, corn, calcium stearate, zinc stearate, waxes, boric acid, hydrogenated vegetable oil, sodium chlorate, magnesium lauryl sulfate, sodium oleate, sodium acetate, sodium benzoate, stearic acid, fatty acid, fumaric acid, glyceryl palmito sulphate, sodium stearyl fumarate or mixtures thereof.
According to one embodiment of the present invention, the amount of lubricants/glidants is between 0.05% and 4.0% by weight in the total formulation. Preferably, it is between 0.1% and 3.0% by weight in the total formulation.
According to one embodiment of the present invention, the lubricant/glidant is magnesium stearate.
As used here in, ‘particle size distribution’ means the cumulative volume size distribution as tested by any conventionally accepted method such as the laser diffraction method (i.e. malvern analysis) .The term d(0.9) means, the size at which 90% by volume of the particles are finer.
According to one embodiment of the present invention, the tablet comprises apixaban having a particle size of d(0.9) greater than 90 pm.
According to one embodiment of the present invention, preferably, the tablet comprises apixaban having a particle size of d(0.9) 90 pm to 99 pm.
According to one embodiment of the present invention, the tablet comprises;
• 0.5 - 10.0% by weight of apixaban
• solvent
• 0.5 - 10.0% by weight of polyvinylpyrrolidone
• 1.0 - 20.0% by weight of starch
• 30.0 - 45.0% by weight of microcrystalline cellulose
• 0.5 - 8.0% by weight of sodium lauryl sulfate
• 1.0 - 5.0% by weight of croscarmellose sodium
• 0.05 - 4.0% by weight of magnesium stearate of the total tablet.
The tablet of the present invention may be prepared, using standard techniques and manufacturing processes well known in the art, such as direct compression, wet or dry granulation, hot melt granulation, hot melt extrusion, fluidized bed granulation, extrusion/spheronization, slugging, spray drying and solvent evaporation.
According to one embodiment of the present invention, the tablet is obtained by using a wet granulation method therefore, a simple and low-cost production method was employed.
It was recognized that because of the targeted low dose for apixaban, content uniformity of the final product becomes an important product attribute. Content uniformity is a pharmaceutical analysis parameter for the quality control of tablets. Thanks to the described methods at the present invention, the tablet which have low dose of apixaban, have been developed with a desired uniformity of content.
Example 1 : The tablet formulation comprising apixaban
q.s: Quantity sufficient
Example 2: The tablet formulation comprising apixaban
Process for example 1 or 2; a) Dissolving apixaban in a solvent, b) Adding polyvinylpyrrolidone in the solvent and dissolving polyvinylpyrrolidone and then obtained granulation solution, c) Mixing starch, lactose and microcrystalline cellulose and charging the mixture to fluid bed granulator-dryer, d) Then, coating the mixture with the granulation solution comprising apixaban using spray granulation, e) Adding sodium lauryl sulfate and croscarmellose sodium and then mixing, f) Adding magnesium stearate and then mixing, g) Compressing to form of tablets, h) Coating tablets with coating agents.
Claims
1 . A tablet comprising apixaban, wherein apixaban and at least one binder are dissolved in solvent.
2. The tablet according to claim 1 , wherein the weight ratio of at least one binder to apixaban is between 1 :1 and 5:1.
3. The tablet according to claim 2, wherein binders are selected from the group comprising polyvinylpyrrolidone, sodium carboxymethyl cellulose, crospovidone, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, glucose, natural gums, sucrose, sodium alginate, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, carboxy methyl cellulose, methyl cellulose, gelatin, carrageenan, guar gum, carbomer, polymethacrylates, methacrylate polymers, gelatin, alginate, alginic acid, xanthan gum, hyaluronic acid, pectin, polysaccharides, carbomer, poloxamer, polyacrylamide, polyoxyethylene-alkyl ether, polydextrose, polyethylene oxide or mixtures thereof.
4. The tablet according to claim 3, wherein the amount of binders is between 0.5% and 10.0% by weight in the total formulation.
5. The tablet according to claim 3, wherein the binder is polyvinylpyrrolidone.
6. The tablet according to claim 1 , wherein solvent is selected from the group comprising dichloromethane, isopropyl alcohol, ethanol, methanol, acetonitrile, dimethyl sulfoxide, dimethylformamide, ethyl acetate, acetone or mixtures.
7. The tablet according to claim 1 , further comprising at least one pharmaceutically acceptable excipient which is selected from the group comprising fillers, disintegrants, surfactants, lubricants/glidants, coating agents or mixtures.
8. The tablet according to claim 7, wherein fillers are selected from the group comprising microcrystalline cellulose, lactose, mannitol, spray-dried mannitol, lactose monohydrate, dextrose, sucrose, fructose, maltose, sorbitol, xylitol, inorganic salts, calcium salts, polysaccharides, dicalcium phosphate, sodium chloride, dextrates, lactitol, maltodextrin, sucrose-maltodextrin mixture, trehalose, sodium carbonate, sodium bicarbonate, calcium carbonate or mixtures thereof.
9. The tablet according to claim 8, wherein the amount of fillers is between 50.0% and 95.0% by weight in the total formulation.
10. The tablet according to claim 8, wherein the filler is microcrystalline cellulose or lactose or mixtures thereof.
11. The tablet according to claim 7, wherein disintegrants are selected from the group comprising croscarmellose sodium, starch, crospovidone, low-substituted hydroxypropyl cellulose, sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, carboxymethyl cellulose, docusate sodium, guar gum, low substituted hydroxypropyl cellulose, polyacryline potassium, sodium alginate, corn starch, sodium starch glycolate, alginic acid, alginates, ion-exchange resins, magnesium aluminium silica, sodium dodesyl sulphate, poloxamer, sodium glycine carbonate or mixtures thereof.
12. The tablet according to claim 11 , wherein the amount of disintegrants is between 2.0% and 25.0% by weight in the total formulation.
13. The tablet according to claim 11 , wherein the disintegrant is croscarmellose sodium or starch or mixtures thereof.
14. The tablet according to claim 7, wherein surfactants are selected from the group comprising sodium lauryl sulphate, sodium docusate, glyceryl monooleate, polyethylene alkyl ether, polyoxyethylene sorbitan fatty acid ester, sorbic acid, sorbitan fatty acid ester, polyoxyethylene stearates, polyethylene glycol, sodium benzoate, docusate sodium, alpha tocopherol, ascorbyl palmitate, citric acid, polyethoxylated fatty acid esters, polyoxyethylene hydrogenated castor oil or mixtures thereof.
15. The tablet according to claim 14, wherein the amount of surfactants is between 0.5% and 8.0% by weight in the total formulation.
16. The tablet according to claim 14, wherein the surfactant is sodium lauryl sulphate.
17. The tablet according to claim 7, wherein lubricants/glidants are selected from the group comprising from magnesium stearate, talc, colloidal silicon dioxide, corn, calcium stearate, zinc stearate, waxes, boric acid, hydrogenated vegetable oil, sodium chlorate, magnesium lauryl sulfate, sodium oleate, sodium acetate, sodium benzoate, stearic acid, fatty acid, fumaric acid, glyceryl palmito sulphate, sodium stearyl fumarate or mixtures thereof.
18. The tablet according to claim 17, wherein the amount of lubricants/glidants is between 0.05% and 4.0% by weight in the total formulation.
19. The tablet according to any preceding claims, wherein the tablet comprising;
0.5 - 10.0% by weight of apixaban solvent
0.5 - 10.0% by weight of polyvinylpyrrolidone
1 .0 - 20.0% by weight of starch
30.0 - 45.0% by weight of microcrystalline cellulose
0.5 - 8.0% by weight of sodium lauryl sulfate
1 .0 - 5.0% by weight of croscarmellose sodium
0.05 - 4.0% by weight of magnesium stearate of the total tablet.
21. Process for preparing the tablet according to claim 20, comprising the following steps; wherein a) Dissolving apixaban in a solvent, b) Adding polyvinylpyrrolidone in the solvent and dissolving polyvinylpyrrolidone and then obtained granulation solution, c) Mixing starch, lactose and microcrystalline cellulose and charging the mixture to fluid bed granulator-dryer, d) Then, coating the mixture with the granulation solution comprising apixaban using spray granulation, e) Adding sodium lauryl sulfate and croscarmellose sodium and then mixing, f) Adding magnesium stearate and then mixing, g) Compressing to form of tablets, h) Coating tablets with coating agents.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP21838041.8A EP4178577A4 (en) | 2020-07-07 | 2021-05-07 | TABLET COMPRISING APIXABAN |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TR2020/10729 | 2020-07-07 | ||
| TR2020/10729A TR202010729A1 (en) | 2020-07-07 | 2020-07-07 | A tablet comprising apixaban |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2022010437A1 true WO2022010437A1 (en) | 2022-01-13 |
Family
ID=79552638
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/TR2021/050445 Ceased WO2022010437A1 (en) | 2020-07-07 | 2021-05-07 | A tablet comprising apixaban |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP4178577A4 (en) |
| TR (1) | TR202010729A1 (en) |
| WO (1) | WO2022010437A1 (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190022008A1 (en) * | 2016-01-12 | 2019-01-24 | Sunshine Lake Pharma Co., Ltd. | Apixaban solid composition and preparation method thereof |
| TR201717703A2 (en) * | 2017-11-10 | 2019-05-21 | Ali Raif Ilac Sanayi Ve Ticaret Anonim Sirketi | APIXABAN FORMULATIONS |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105982870B (en) * | 2015-02-03 | 2020-05-01 | 山东新时代药业有限公司 | Apixaban tablet |
| CN108553441B (en) * | 2018-06-08 | 2019-11-08 | 北京阳光诺和药物研究有限公司 | A kind of Apixaban tablet and preparation method thereof |
-
2020
- 2020-07-07 TR TR2020/10729A patent/TR202010729A1/en unknown
-
2021
- 2021-05-07 WO PCT/TR2021/050445 patent/WO2022010437A1/en not_active Ceased
- 2021-05-07 EP EP21838041.8A patent/EP4178577A4/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190022008A1 (en) * | 2016-01-12 | 2019-01-24 | Sunshine Lake Pharma Co., Ltd. | Apixaban solid composition and preparation method thereof |
| TR201717703A2 (en) * | 2017-11-10 | 2019-05-21 | Ali Raif Ilac Sanayi Ve Ticaret Anonim Sirketi | APIXABAN FORMULATIONS |
Non-Patent Citations (1)
| Title |
|---|
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Also Published As
| Publication number | Publication date |
|---|---|
| TR202010729A1 (en) | 2022-01-21 |
| EP4178577A1 (en) | 2023-05-17 |
| EP4178577A4 (en) | 2024-04-24 |
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