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Emtricitabine / Tenofovir

The Miriam Hospital · FDA-approved active Small molecule

Emtricitabine and tenofovir are nucleoside/nucleotide reverse transcriptase inhibitors that block HIV replication by inhibiting the enzyme responsible for converting viral RNA into DNA.

Emtricitabine and tenofovir are nucleoside/nucleotide reverse transcriptase inhibitors that block HIV replication by inhibiting the enzyme responsible for converting viral RNA into DNA. Used for HIV-1 infection (treatment), HIV-1 pre-exposure prophylaxis (PrEP).

At a glance

Generic nameEmtricitabine / Tenofovir
SponsorThe Miriam Hospital
Drug classNucleoside/nucleotide reverse transcriptase inhibitor (NRTI/NtRTI) combination
TargetHIV reverse transcriptase
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

Both drugs are antiretroviral agents that work by inhibiting HIV reverse transcriptase, an enzyme essential for viral replication. Emtricitabine is a cytidine nucleoside analog, while tenofovir is a nucleotide analog; both are incorporated into the growing viral DNA chain, causing chain termination and preventing the virus from replicating. This combination is commonly used as part of highly active antiretroviral therapy (HAART) regimens.

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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