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Details for Patent: 5,725,878

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Details for Patent: 5,725,878

Title: Pharmaceutical composition comprising HIV protease inhibiting compounds
Abstract:A pharmaceutical composition is disclosed which comprises a solution of an HIV protease inhibiting compound in a pharmaceutically acceptable organic solvent comprising a pharmaceutically acceptable alcohol. The composition can optionally comprise a pharmaceutically acceptable acid or a combination of pharmaceutically acceptable acids. The solution can optionally be encapsulated in hard gelatin capsules or soft elastic gelatin capsules. The solution can optionally be granulated with a pharmaceutically acceptable granulating agent.
Inventor(s): Al-Razzak; Laman A. (Libertyville, IL), Marsh; Kennan C. (Lake Forest, IL), Kaul; Dilip (Waukegan, IL), Manning; Lourdes P. (Grayslake, IL)
Assignee: Abbott Laboratories (Abbott Park, IL)
Filing Date:May 04, 1995
Application Number:08/435,009
Claims:1. A solid pharmaceutical composition comprising a mixture of (A) a solution of (1) an HIV protease inhibiting compound in the amount of from about 4% to about 30% by weight of the total solution, wherein the HIV protease inhibiting compound is selected from the group consisting of:

N-(2(R)-hydroxy-1(S)-indanyl)-2(R)-phenylmethyl-4(S)-hydroxy-5-(1-(4-(3-pyr idylmethyl)-2(S)-N'-(t-butylcarboxamido)-piperazinyl))-pentaneamide;

N-tert-butyl-decahydro-2-(2(R)-hydroxy-4-phenyl-3(S)-((N-(N-2-quinolylcarbo nyl)-L-asparaginyl)amino)butyl)-(4aS,8aS)-isoquinoline-3(S)-carboxamide;

5(S)-Boc-amino-4(S)-hydroxy-6-phenyl-2(R)-phenylmethylhexanoyl-(L)-Val-(L)- Phe-morpholin-4-ylamide;

1-Naphthoxyacetyl-beta-methylthio-Ala-(2S,3S)-3-amino-2-hydroxy-4-butanoyl- 1,3-thiazolidine-4-t-butylamide;

5-isoquinolinoxyacetyl-beta-methylthio-Ala-(2S,3S)-3-amino-2-hydroxy-4-buta noyl-1,3-thlazolidine-4-t-butylamide;

(1S-(1R*(R*),2S*))-N.sup.1 (3-((((1,1-dimethylethyl)amino)carbonyl)(2-methylpropyl)aminol-2-hydroxy-1 -(phenylmethyl)propyl)-2-((2-quinolinylcarbonyl)amino)-butanediamide; ##STR6## and (2) a total of from about 0.2 to about 2 molar equivalents (based on the HIV protease inhibiting compound) of (i) a pharmaceutically acceptable acid or (ii) a mixture of pharmaceutically acceptable acids in a pharmaceutically acceptable organic solvent comprising a mixture of (a) a pharmaceutically acceptable alcohol or mixture of pharmaceutically acceptable alcohols in a total amount of from about 2% to about 50% by weight of the total solution, said alcohol or mixture of alcohols being a liquid at about room temperature and (b) a pharmaceutically acceptable solvent or a mixture of pharmaceutically acceptable solvents in a total amount of from about 20% to about 60% by weight of the total solution, said solvent or mixture of solvents having a melting point between about 20.degree. C. and about 60.degree. C., said solvent or mixture of solvents being miscible with the alcohol or mixture of alcohols and providing a homogeneous mixture with the alcohol or mixture of alcohols, said homogeneous mixture being a solid or semi-solid at about 20.degree. C. and (B) a pharmaceutically acceptable granulating agent or a mixture of pharmaceutically acceptable granulating agents.

2. The composition of claim 1 wherein the solid mixture is encapsulated in a hard gelatin capsule.

3. A solid pharmaceutical composition comprising a mixture of (A) a solution of (1) (2S,3S,5S)-5-(N-(N-((N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)-amino)ca rbonyl)valinyl)-amino)-2-(N-((5-thiazolyl)methoxycarbonyl)amino)-1,6-diphen yl-3-hydroxyhexane in the amount of from about 4% to about 30% by weight of the total solution and (2) a total of from about 0.2 to about 2 molar equivalents (based on the compound of part (1)) of (i) a pharmaceutically acceptable acid or (ii) a mixture of pharmaceutically acceptable acids in a pharmaceutically acceptable organic solvent comprising a mixture of (a) propylene glycol in the amount of from about 5% to about 40% by weight of the total solution, (b) ethanol in the amount of from about 2% to about 20%, and (c) polyethylene glycol 540 in the amount of from about 20% to about 60% or a total amount of from about 20% to about 60% by weight of the total solution of (i) a saturated polyglycolized glyceride or (ii) a mixture of saturated polyglycolized glycerides and (B) a pharmaceutically acceptable granulating agent or a mixture of pharmaceutically acceptable granulating agents.

4. The composition of claim 3 wherein the solid mixture is encapsulated in a hard gelatin capsule.
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