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Tenofovir alafenamide/emtricitabine

ViiV Healthcare · FDA-approved active Small molecule

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

Tenofovir alafenamide and emtricitabine are nucleotide/nucleoside reverse transcriptase inhibitors that block HIV replication by inhibiting the enzyme responsible for converting viral RNA into DNA. Used for HIV-1 infection in treatment-naïve and treatment-experienced adults, HIV-1 pre-exposure prophylaxis (PrEP) in at-risk individuals.

At a glance

Generic nameTenofovir alafenamide/emtricitabine
Also known asTAF, FTC
SponsorViiV Healthcare
Drug classNucleotide/nucleoside reverse transcriptase inhibitor combination
TargetHIV reverse transcriptase
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Tenofovir alafenamide (TAF) is a prodrug of tenofovir that achieves higher intracellular concentrations with lower systemic exposure compared to tenofovir disoproxil fumarate. Emtricitabine (FTC) is a cytidine analog that inhibits reverse transcriptase. Together, they prevent HIV from integrating into the host genome and establishing persistent infection.

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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