Last reviewed · How we verify

Tenofovir, Emtricitabine, Raltegravir

Hospital Clinic of Barcelona · FDA-approved active Small molecule

This combination of three antiretroviral drugs inhibits HIV replication by blocking reverse transcriptase and integrase enzymes, preventing viral DNA synthesis and integration into the host genome.

This combination of three antiretroviral drugs inhibits HIV replication by blocking reverse transcriptase and integrase enzymes, preventing viral DNA synthesis and integration into the host genome. Used for HIV-1 infection in treatment-naïve and treatment-experienced patients, HIV-1 infection as part of combination antiretroviral therapy.

At a glance

Generic nameTenofovir, Emtricitabine, Raltegravir
SponsorHospital Clinic of Barcelona
Drug classAntiretroviral combination therapy (NRTI/NtRTI + INSTI)
TargetHIV reverse transcriptase and HIV integrase
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

Tenofovir and emtricitabine are nucleotide/nucleoside reverse transcriptase inhibitors (NRTIs/NtRTIs) that block the reverse transcriptase enzyme, preventing conversion of viral RNA to DNA. Raltegravir is an integrase strand transfer inhibitor (INSTI) that prevents integration of viral DNA into the host chromosome. Together, they provide complementary mechanisms to suppress HIV replication.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: