Anti-retroviral combination

US9339470B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9339470-B2
Application numberUS-81030108-A
CountryUS
Kind codeB2
Filing dateDec 24, 2008
Priority dateDec 24, 2007
Publication dateMay 17, 2016
Grant dateMay 17, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A pharmaceutical composition comprising a solid unit dosage form comprising: (i) ritonavir or a pharmaceutically acceptable salt and ester thereof; (ii) darunavir or a pharmaceutically acceptable salt and ester thereof.

First claim

Opening claim text (preview).

The invention claimed is: 1. A pharmaceutical compositon comprising a tablet dosage form comprising: a first layer comprising ritonavir in an amount of 50 mg, collidal silicon dioxide, vinylpyrrolidone-vinyl acetate copolymer, polyoxl 40 hydrogenated castor oil, and dibasic calcium phosphate, and wherein the first layer is absent of darunavir ethanolate; and a second layer comprising the darunavir ethanolate in an amount of 325 mg, microcrystalline cellulose, crospovidone, povidone, collidal silicon dioxide, and magnesium stearate, and wherein the second layer is absent of the ritonavir. 2. The pharmaceutical composition according to claim 1 , wherein the ritonavir of the first layer is present in granules obtained via hot melt extrusion with the collidal silicon dioxide, the vinylpyrrolidone-vinyl acetate copolymer, and the poloxyl 40 hydrogenated castor oil. 3. The pharmaceutical composition according to claim 2 , wherein a melting temperature for the hot melt extrusion ranges from 70° to 200° C. 4. The pharmaceutical composition according to claim 1 , wherein a ratio of the weight of the ritonavir to the weight of the vinylpyrrolidone-vinyl acetate copolymer is from 1:1 to 1:6. 5. The pharmaceutical composition according to claim 1 , wherein the darunavir ethanolate of the second layer is present in granules obtained via wet granulation with povidone. 6. A method of treating HIV or AIDS comprising administering a therapeutically effective amount of the pharmaceutical composition as defined in claim 1 . 7. The pharmaceutical composition according to claim 1 , wherein the tablet dosage form has a film coating. 8. A pharmaceutical composition comprising a tablet dosage form comprising: a first layer comprising ritonavir in an amount of 100 mg, colloidal silicon dioxide, yinylpyrrolidone-vinyl acetate copolymer, sorbitan monolaurate, crospovidone, microcrystalline cellulose, and sodium stearyl monostearate, and wherein the first layer is absent of darunavir; and a second layer comprising the danmavir in an amount of 300 mg, crospovidone, povidone, yellow iron oxide, microcrystalline cellulose, colloidal silicon dioxide, and magnesium stearate, and wherein the second layer is absent of the ritonavir. 9. The pharmaceutical composition according to claim 8 , wherein the ritonavir of the first layer is present in granules obtained via hot melt extrusion with the colloidal silicon dioxide, the yinylpyrrolidone-vinyl acetate copolymer, and sorbitan monolaurate. 10. The pharmaceutical composition according to claim 9 , wherein a melting temperature for the hot melt, extrusion ranges from 70° C. to 200° C. 11. The pharmaceutical composition according to claim 8 , wherein the darunavir of the second layer is present in granules obtained via wet granulation with purified water. 12. The pharmaceutical composition according to claim 8 , wherein a ratio of the weight of the ritonavir to the weight of the vinylpyrrolidone-vinyl acetate copolymer is from 1:1 to 1:6. 13. The pharmaceutical composition according to claim 8 , wherein the tablet dosage form has a film coating. 14. A method of treating HIV or AIDS comprising administering a therapeutically effective amount of the pharmaceutical composition as defined in claim 8 .

Assignees

Inventors

Classifications

  • for HIV · CPC title

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • Tabletting processes · CPC title

  • A61K9/209Primary

    containing drug in at least two layers or in the core and in at least one outer layer · CPC title

  • Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets · CPC title

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What does patent US9339470B2 cover?
A pharmaceutical composition comprising a solid unit dosage form comprising: (i) ritonavir or a pharmaceutically acceptable salt and ester thereof; (ii) darunavir or a pharmaceutically acceptable salt and ester thereof.
Who is the assignee on this patent?
Lulla Amar, Malhotra Geena, Cipla Ltd
What technology area does this patent fall under?
Primary CPC classification A61K9/209. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue May 17 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).