US2020171027A1PendingUtilityA1

Combinations of a pyrimidine containing nnrti with rt inhibitors

Assignee: JANSSEN SCIENCES IRELAND UCPriority: Sep 3, 2003Filed: Feb 7, 2020Published: Jun 4, 2020
Est. expirySep 3, 2023(expired)· nominal 20-yr term from priority
Inventors:Paul Stoffels
A61K 31/505A61K 31/513A61K 31/675A61K 31/52A61K 9/20A61K 31/519A61P 43/00A61P 37/04A61P 31/18A61K 31/506A61K 9/2027
70
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Claims

Abstract

The present invention concerns combinations of a pyrimidine containing NNRTI with nucleoside reverse transcriptase inhibitors and nucleotide reverse transcriptase inhibitors useful for the treatment of HIV infected patients or for the prevention of HIV transmission or infection.

Claims

exact text as granted — not AI-modified
1 . A combination comprising
 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile, or a stereoisomeric form thereof; or a pharmaceutically acceptable salt thereof,   lamivudine, and   abacavir or a pharmaceutically acceptable salt thereof;   wherein the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile, or a stereoisomeric form thereof; or a pharmaceutically acceptable salt thereof; the lamivudine; and the abacavir or pharmaceutically acceptable salt thereof are therapeutically effective HIV inhibitors at a dose that can be administered once daily.   
     
     
         2 . The combination of  claim 1 , wherein the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile, or a stereoisomeric form thereof; or a pharmaceutically acceptable salt thereof, is E-4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile. 
     
     
         3 . The method of  claim 1 , wherein the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile, or a stereoisomeric form thereof; or a pharmaceutically acceptable salt thereof, is E-4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile hydrochloride. 
     
     
         4 . The combination of  claim 1 , comprising between 10 mg and 500 mg of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile or a stereoisomeric form thereof. 
     
     
         5 . The combination of  claim 1 , comprising between 10 mg and 300 mg of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile or a stereoisomeric form thereof. 
     
     
         6 . The combination of  claim 1 , comprising about 25 mg of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]-amino]-2-pyrimidinyl]-amino]-benzonitrile or a stereoisomeric form thereof. 
     
     
         7 . The combination of  claim 1 , comprising about 150 mg of the lamivudine. 
     
     
         8 . The combination of  claim 1 , comprising abacavir sulfate. 
     
     
         9 . The combination of  claim 1 , comprising about 300 mg of the abacavir, or a pharmaceutically acceptable salt thereof. 
     
     
         10 . The combination of  claim 1 , further comprising zidovudine. 
     
     
         11 . The combination of  claim 10 , wherein the combination comprises about 300 mg of zidovucine. 
     
     
         12 . The combination of  claim 1 , as a unitary pharmaceutically acceptable formulation. 
     
     
         13 . The combination of  claim 12 , wherein the unitary pharmaceutically acceptable formulation is selected from the group consisting of tablets, capsules, parenteral compositions, injectable solutions, and injectable suspensions. 
     
     
         14 . The combination of  claim 12 , wherein the unitary pharmaceutically acceptable formulation is a tablet. 
     
     
         15 . A method of treating HIV infection in a patient comprising administering to the patient the combination of  claim 1  once daily.

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