Drug intelligence / Profile preview

maraviroc + saquinavir + ritonavir

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral
01

Overview

A combination of **maraviroc**, **saquinavir**, and **ritonavir** used for the treatment of HIV-1 infection. Maraviroc is a small molecule antagonist of the CCR5 receptor, blocking HIV-1 entry into CD4+ cells. Saquinavir is a small molecule inhibitor of the HIV-1 protease enzyme, preventing maturation of infectious viral particles. Ritonavir is primarily used here as a pharmacokinetic enhancer, inhibiting CYP3A-mediated metabolism to increase plasma concentrations of saquinavir and maraviroc, but also has direct protease inhibitor effects. This regimen is used in antiretroviral-experienced adults and is considered when viral resistance or specific intolerance makes alternative regimens less suitable. Dose adjustments are required due to significant pharmacokinetic interactions among the components[1][2][3][7].

02

Targets

CYP3A4 (Cytochrome P450 3A4)CCR5 (C-C chemokine receptor type 5)PR (Progesterone receptor)

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