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Entecavir+Carvedilol

ShuGuang Hospital · FDA-approved active Small molecule

This combination uses entecavir to inhibit hepatitis B virus reverse transcriptase and carvedilol to block beta-adrenergic receptors, addressing both viral replication and portal hypertension complications.

This combination uses entecavir to inhibit hepatitis B virus reverse transcriptase and carvedilol to block beta-adrenergic receptors, addressing both viral replication and portal hypertension complications. Used for Chronic hepatitis B with advanced fibrosis or cirrhosis, Hepatitis B-related portal hypertension with variceal bleeding risk.

At a glance

Generic nameEntecavir+Carvedilol
SponsorShuGuang Hospital
Drug classAntiviral + Beta-blocker combination
TargetHBV reverse transcriptase; beta-1, beta-2, and alpha-1 adrenergic receptors
ModalitySmall molecule
Therapeutic areaHepatology / Infectious Disease
PhaseFDA-approved

Mechanism of action

Entecavir is a nucleoside reverse transcriptase inhibitor that suppresses HBV replication by blocking viral polymerase activity. Carvedilol is a non-selective beta-blocker with alpha-blocking properties that reduces portal pressure and decreases variceal bleeding risk in patients with advanced liver disease. The combination targets both the underlying viral infection and hemodynamic complications of cirrhosis.

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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