Abstract
A prospective, open-label study was conducted to assess the response to indinavir, efavirenz, and adefovir in human immunodeficiency virus (HIV)-infected patients experiencing viral rebound while receiving therapy with nelfinavir-containing regimens, to determine whether the protease genotype influenced the outcome of the salvage regimen. Genotyping from 29 nelfinavir failures revealed D30N in 17 (59%) and L90M in 11 (38%) cases. Suppression to <400 viral RNA copies/mL was achieved at week 48 in 56% of patients with the D30N virus versus 18% of patients with the L90M virus.
MeSH terms
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Adenine / analogs & derivatives
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Adenine / pharmacology
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Adenine / therapeutic use*
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Adult
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Alkynes
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Anti-HIV Agents / therapeutic use
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Benzoxazines
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Cyclopropanes
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Drug Resistance, Viral
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Female
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HIV / drug effects
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HIV / genetics
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HIV Infections / drug therapy*
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HIV Protease Inhibitors / therapeutic use
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Humans
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Indinavir / pharmacology
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Indinavir / therapeutic use*
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Male
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Middle Aged
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Nelfinavir / pharmacology
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Nelfinavir / therapeutic use*
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Organophosphonates*
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Oxazines / pharmacology
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Oxazines / therapeutic use*
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Treatment Failure
Substances
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Alkynes
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Anti-HIV Agents
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Benzoxazines
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Cyclopropanes
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HIV Protease Inhibitors
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Organophosphonates
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Oxazines
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Indinavir
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adefovir
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Nelfinavir
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Adenine
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efavirenz