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Reducing dose of Lopinavir

University Hospital, Geneva · FDA-approved active Small molecule

Lopinavir is a protease inhibitor that blocks HIV protease, preventing the cleavage of viral polyproteins and thereby inhibiting HIV replication.

Lopinavir is a protease inhibitor that blocks HIV protease, preventing the cleavage of viral polyproteins and thereby inhibiting HIV replication. Used for HIV-1 infection (in combination with ritonavir and other antiretroviral agents).

At a glance

Generic nameReducing dose of Lopinavir
SponsorUniversity Hospital, Geneva
Drug classHIV protease inhibitor
TargetHIV protease
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Lopinavir binds to the active site of HIV protease, a viral enzyme essential for processing precursor polyproteins into mature, functional viral proteins. By preventing this proteolytic cleavage, lopinavir causes the production of immature, non-infectious viral particles. This mechanism is the basis for its antiretroviral activity, and dose reduction is typically employed to minimize toxicity while maintaining therapeutic efficacy, often in combination with other antiretroviral agents.

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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