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Maraviroc, Darunavir/r

Catholic University of the Sacred Heart · FDA-approved active Small molecule

This combination uses maraviroc to block HIV entry via the CCR5 co-receptor and darunavir/ritonavir to inhibit HIV protease, together suppressing viral replication through dual mechanisms.

This combination uses maraviroc to block HIV entry via CCR5 co-receptors and darunavir/ritonavir to inhibit HIV protease, together suppressing viral replication through dual mechanisms. Used for HIV-1 infection in treatment-experienced patients with CCR5-tropic virus.

At a glance

Generic nameMaraviroc, Darunavir/r
SponsorCatholic University of the Sacred Heart
Drug classAntiretroviral combination (CCR5 antagonist + protease inhibitor)
TargetCCR5 co-receptor (maraviroc); HIV protease (darunavir)
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

Maraviroc is a CCR5 antagonist that prevents HIV from binding to and entering CD4+ T cells by blocking the CCR5 chemokine receptor on the cell surface. Darunavir is a protease inhibitor that blocks HIV protease, preventing the cleavage of viral polyproteins necessary for infectious particle maturation, while ritonavir acts as a pharmacokinetic booster. Together, they provide complementary antiretroviral activity against HIV-1.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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