Abstract
Currently, the optimal boosting dose for saquinavir is unknown. Therefore, we evaluated the pharmacokinetics profiles in a cross over setting comparing saquinavir/ritonavir 1500/50 mg (plus NRTI backbone) to saquinavir/ritonavir 1500/100 mg in the same HIV-infected, Thai individuals. The 50% reduction of ritonavir boosting did not result in a change in the pharmacokinetics of saquinavir, whereas the ritonavir exposure was significantly lower when a dose of 50 mg was administered.
Publication types
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Clinical Trial, Phase II
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Anti-HIV Agents / administration & dosage*
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Anti-HIV Agents / blood
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Anti-HIV Agents / pharmacokinetics
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Cross-Over Studies
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Dose-Response Relationship, Drug
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Drug Administration Schedule
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Female
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HIV Infections / blood
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HIV Infections / drug therapy*
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HIV-1 / drug effects*
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Humans
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Male
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Middle Aged
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Ritonavir / administration & dosage*
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Ritonavir / blood
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Ritonavir / pharmacokinetics
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Saquinavir / administration & dosage*
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Saquinavir / blood
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Saquinavir / pharmacokinetics
Substances
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Anti-HIV Agents
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Saquinavir
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Ritonavir