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Atazanavir/Ritonavir + Famotidine

Bristol-Myers Squibb · FDA-approved active Small molecule

Atazanavir inhibits HIV protease to prevent viral replication, while ritonavir boosts atazanavir levels, and famotidine reduces gastric acid to improve atazanavir absorption.

Atazanavir inhibits HIV protease to prevent viral replication, while ritonavir boosts atazanavir levels, and famotidine reduces gastric acid to improve atazanavir absorption. Used for HIV-1 infection in treatment-naïve and treatment-experienced adults.

At a glance

Generic nameAtazanavir/Ritonavir + Famotidine
Also known asReyataz
SponsorBristol-Myers Squibb
Drug classHIV protease inhibitor (boosted) + H2-receptor antagonist
TargetHIV protease; CYP3A4 (ritonavir); H2 receptor (famotidine)
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

Atazanavir is an HIV protease inhibitor that blocks the viral protease enzyme, preventing the maturation of HIV particles and reducing viral load. Ritonavir is a pharmacokinetic booster that inhibits cytochrome P450 metabolism, significantly increasing atazanavir plasma concentrations and allowing for lower, more convenient dosing. Famotidine, an H2-receptor antagonist, reduces gastric acid production to optimize the pH-dependent absorption of atazanavir in the gastrointestinal tract.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results