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Adefovir/Entecavir

Bristol-Myers Squibb · FDA-approved active Small molecule

Adefovir and entecavir are nucleoside/nucleotide reverse transcriptase inhibitors that block hepatitis B virus (HBV) replication by inhibiting viral polymerase.

Adefovir and entecavir are nucleoside/nucleotide reverse transcriptase inhibitors that block hepatitis B virus (HBV) replication by inhibiting viral polymerase. Used for Chronic hepatitis B infection, Lamivudine-resistant hepatitis B (adefovir).

At a glance

Generic nameAdefovir/Entecavir
Also known asBaraclude, BMS-200475
SponsorBristol-Myers Squibb
Drug classNucleoside/nucleotide reverse transcriptase inhibitor
TargetHepatitis B virus polymerase (reverse transcriptase)
ModalitySmall molecule
Therapeutic areaVirology/Infectious Disease
PhaseFDA-approved

Mechanism of action

Both drugs are nucleoside analogues that are phosphorylated intracellularly and incorporated into the growing HBV DNA chain, causing chain termination and preventing viral replication. Entecavir is a guanosine analogue with higher potency and lower resistance rates compared to adefovir. Adefovir is an adenosine monophosphate analogue that also inhibits HBV polymerase with activity against lamivudine-resistant strains.

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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