Last reviewed · How we verify

AZT

Johns Hopkins Bloomberg School of Public Health · FDA-approved active Small molecule

AZT (zidovudine) inhibits HIV reverse transcriptase, preventing the virus from converting its RNA genome into DNA and replicating within host cells.

AZT (zidovudine) inhibits HIV reverse transcriptase, preventing the virus from converting its RNA genome into DNA and replicating within host cells. Used for HIV-1 infection (treatment), Prevention of maternal-fetal HIV transmission (perinatal prophylaxis).

At a glance

Generic nameAZT
Also known asZidovuidne (ZDV), Zidovudine
SponsorJohns Hopkins Bloomberg School of Public Health
Drug classNucleoside reverse transcriptase inhibitor (NRTI)
TargetHIV reverse transcriptase
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

AZT is a nucleoside reverse transcriptase inhibitor (NRTI) that acts as a chain terminator during HIV DNA synthesis. When incorporated into the growing DNA chain by reverse transcriptase, it lacks a 3'-OH group, causing premature chain termination and blocking viral replication. This was the first antiretroviral drug approved for HIV treatment and remains part of combination antiretroviral therapy regimens.

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: