Claims for Patent: 9,763,885

Summary for Patent: 9,763,885

Title:	Oral tablet formulation consisting of fixed combination of rosuvastatin and ezetimibe for treatment of hyperlipidemia and cardiovascular diseases
Abstract:	The present invention is an orally consumed fixed combination formulation of both rosuvastatin and ezetimibe in one tablet that is expected to have the same Area Under Curve as two active ingredients taken together individually orally, and pharmaceutically acceptable additives suitable for the preparation. In preferred embodiments of this invention, the rosuvastatin is in the form of rosuvastatin calcium and the pharmaceutically acceptable additives are selected from diluents, disintegrants, glidants, lubricants, colorants and combinations thereof.
Inventor(s):	Dias; Marie Charmaine (Morristown, NJ)
Assignee:	Althera Laboratories Ltd. (Dublin, IE)
Application Number:	14/350,905
Patent Claims:	1. A solid dosage form comprising rosuvastatin and ezetimibe combined in one bilayer tablet comprising rosuvastatin in a first layer and ezetimibe in a microcrystalline cellulose free second layer, and wherein: (i) the solid dosage form when orally administered to healthy individuals is bioequivalent to corresponding dosages of rosuvastatin and ezetimibe taken together individually orally; (ii) the solid dosage form comprises rosuvastatin and ezetimibe in a weight ratio of 0.5:1, 1:1 or 2:1, and pharmaceutically acceptable additives suitable for the preparation of solid dosage forms comprising a combination of rosuvastatin and ezetimibe; and wherein rosuvastatin is formulated with microcrystalline cellulose in the first layer and ezetimibe is substantially separated from the microcrystalline cellulose of the first layer; and (iii) the said solid dosage form is a stable composition of rosuvastatin and ezetimibe comprising less than 0.5% of ezetimibe related impurities after 6 weeks of storage at 40 .degree. C. and 75% relative humidity, less than 0.5% of rosuvastatin related lactone impurities and less than 0.5% of rosuvastatin related keto impurities after 6 weeks of storage at 40 .degree. C. and 75% relative humidity. 2. The solid dosage form of claim 1, wherein the rosuvastatin dosage ranges from 2.5 mg to 40 mg, and ezetimibe dosage ranges from 5 mg to 20 mg. 3. The solid dosage form of claim 1 comprising no ezetimibe related impurities after 6 weeks of storage at 40.degree. C. and 75% relative humidity, less than 0.2% of rosuvastatin related lactone impurities and less than 0.2% of rosuvastatin related keto impurities after 6 weeks of storage at 40.degree. C. and 75% relative humidity. 4. The solid dosage form of claim 1, wherein the first layer comprising rosuvastatin as the active ingredient further comprises starch in an amount of 1-15% of the weight of the rosuvastatin comprising first layer, dicalcium phosphate in an amount of 0.5-10% of the weight of the rosuvastatin comprising first layer, microcrystalline cellulose in an amount of 20-90% of the weight of the rosuvastatin comprising first layer, and crospovidone in an amount of 2-30% of the weight of the rosuvastatin comprising first layer as excipients, and sodium stearate fumarate as a lubricant in an amount of 0.1-2% of the weight of the rosuvastatin comprising first layer. 5. The solid dosage form of claim 1, wherein the second layer comprising ezetimibe as the active ingredient further comprises sodium lauryl sulphate in an amount of 2-20% of the weight of the ezetimibe comprising second layer and lactose in an amount of 20-90% of the weight of the ezetimibe comprising second layer, as excipient and surfactant; croscaramellose as a disintegrant in an amount of 5-30% of the weight of the ezetimibe comprising second layer, polyvinylpyrrolidone as a binder in an amount of 0.5-10% of the weight of the ezetimibe comprising second layer and magnesium stearate in an amount of 0.2-5% of the weight of the ezetimibe comprising second layer. 6. The solid dosage form of claim 4, wherein the rosuvastatin comprising first layer additionally contains_butylated hydroxy anisole as an antioxidant in an amount of 0.05-2% of the weight of the first layer and fumed silica as a dispersion agent in an amount of 1-10% of the weight of the first layer. 7. A method of making the solid dosage form of claim 1, the method comprising the steps of: a) blending rosuvastatin calcium with pre-gelatinized starch, calcium hydrogen phosphate dihydrate, microcrystalline cellulose and crospovidone to provide a blend, and passing the blend through sieve and lubricating the blend with lubricant to create a rosuvastatin layer blend; b) mixing ezetimibe with a wetting agent and a disperse material in isopropyl alcohol and dichloromethane mixture; c) absorbing the dispersion of step (b) on lactose and mixing thoroughly; d) air drying the dispersion of step (c), passing it through a sieve, mixing with croscarmellose sodium, and blending; e) granulating the mix of step (d) with polyvinylpyrrolidone solution and drying it to obtain ezetimibe granules; f) creating bilayer tablet by compressing the blend of step (a) and the granules of step (e) in a bilayer compression machine followed by film coating. 8. The method of claim 7 wherein the lubricant in step a) is sodium stearyl fumarate and the wetting agent in step b) is sodium lauryl sulfate. 9. A method of treating hyperlipidemia, cardiovascular diseases, congestive heart failure, myocardial infarction, or atherosclerosis, the method comprising administering orally the solid dosage form of claim 1 to a patient in need of such treatment.