The present invention discloses a method for treating HIV that includes administering .beta.-D-D4FC or its pharmaceutically acceptable salt or prodrug to a human in need of therapy in combination or alternation with a drug that induces a mutation in HIV-1 at a location other than the 70(K to N), 90 or the 172 codons of the reverse transcriptase region. Also disclosed is a method for using .beta.-D-D4FC as "salvage therapy" to patients which exhibit drug resistance to other anti-HIV agents. .beta.-D-D4FC can be used generally as salvage therapy for any patient which exhibits resistance to a drug that induces a mutation at other than the 70(K to N), 90 or the 172 codons.

 
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< Gene BN01 mapping to chromosome 16q24.3

< Human choline acetyltransferase

> Purine derivatives

> Phosphoramidate, and mono-, di-, and tri-phosphate esters of (1R, cis)-4-(6-amino-9H-purin-9-yl)-2-cyclopentene-1-methanol as antiviral agents

~ 00291