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"Raltegravir" and "Zidovudine"

Universidad Peruana Cayetano Heredia · FDA-approved active Small molecule

Raltegravir is an integrase inhibitor that blocks HIV integration into host DNA, while zidovudine is a nucleoside reverse transcriptase inhibitor that prevents HIV RNA conversion to DNA.

Raltegravir is an integrase inhibitor that blocks HIV integration into host DNA, while zidovudine is a nucleoside reverse transcriptase inhibitor that prevents HIV RNA-to-DNA conversion; together they provide dual antiretroviral activity. Used for HIV-1 infection in treatment-naïve and treatment-experienced patients.

At a glance

Generic name"Raltegravir" and "Zidovudine"
Also known as"Raltegravir", "Zidovudine"
SponsorUniversidad Peruana Cayetano Heredia
Drug classAntiretroviral combination (integrase inhibitor + nucleoside reverse transcriptase inhibitor)
TargetHIV integrase (raltegravir); HIV reverse transcriptase (zidovudine)
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

This combination targets two critical steps of HIV replication. Raltegravir inhibits the integrase enzyme, preventing the viral genome from integrating into the host chromosome. Zidovudine inhibits reverse transcriptase, blocking the conversion of viral RNA into DNA. 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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