Abstract
We report the results of the extended follow-up at one year of a randomized trial evaluating the virological efficacy of a salvage therapy combining lopinavir and amprenavir with either 200 or 400 mg/day ritonavir, along with optimized nucleoside reverse transcriptase inhibitors, in patients carrying multidrug-resistant isolates. The combination of amprenavir, lopinavir and ritonavir (400 mg/day) is durably potent, yielding a sustained virological response (HIV RNA < 50 copies) in 39% of cases.
Publication types
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Multicenter Study
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Randomized Controlled Trial
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Research Support, Non-U.S. Gov't
MeSH terms
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Anti-HIV Agents / therapeutic use*
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Antiretroviral Therapy, Highly Active
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Carbamates / therapeutic use
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Drug Resistance, Multiple, Viral*
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Follow-Up Studies
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Furans
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HIV Infections / drug therapy*
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HIV Infections / virology
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HIV-1 / drug effects
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Humans
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Lopinavir
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Pyrimidinones / therapeutic use
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Ritonavir / therapeutic use
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Salvage Therapy / methods*
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Sulfonamides / therapeutic use
Substances
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Anti-HIV Agents
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Carbamates
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Furans
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Pyrimidinones
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Sulfonamides
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Lopinavir
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amprenavir
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Ritonavir