A Phase II Trial of Dual Protease Inhibitor Therapy: Amprenavir in Combination With Indinavir, Nelfinavir, or Saquinavir

This study evaluated dual protease inhibitor (PI) regimens containing amprenavir (APV) in Pi-naive, HIV-1-infected patients over 48 weeks. Patients were randomized to 800-mg APV combined with 800-mg indinavir (IDV), 750-mg nelfi navir (NFV), or 800-mg saquinavir-soft gel capsule (SGV-SGC), all three...

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Veröffentlicht in:Journal of acquired immune deficiency syndromes (1999) 2001-04, Vol.26 (5), p.458-461
Hauptverfasser: Eron, Joseph J, Haubrich, Richard, Lang, William, Pagano, Grace, Millard, Judith, Wolfram, Josie, Snowden, Wendy, Pedneault, Louise, Tisdale, Margaret
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Sprache:eng
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Zusammenfassung:This study evaluated dual protease inhibitor (PI) regimens containing amprenavir (APV) in Pi-naive, HIV-1-infected patients over 48 weeks. Patients were randomized to 800-mg APV combined with 800-mg indinavir (IDV), 750-mg nelfi navir (NFV), or 800-mg saquinavir-soft gel capsule (SGV-SGC), all three times daily without nucleoside reverse transcriptase inhibitors, or APV given alone for 3 weeks and then with 150-mg lamivudine (3TC) and 300-mg zidovudine (ZDV), twice daily. Dual PI therapy demonstrated substantial antiviral activity and was generally safe and well tolerated. Eight patients had virologic failure; 5 were receiving dual PI therapy and 3 were in the APV/3TC/ZDV arm. The protease I50V mutation characteristic of APV resistance was not observed, although other key PI mutations were selected in 4 patients failing therapy, 2 of whom had PI resistance at baseline.
ISSN:1525-4135
1944-7884
DOI:10.1097/00042560-200104150-00008