Last reviewed · How we verify

rVSV∆G-ZEBOV-GP

University of Birmingham · FDA-approved active Biologic

A recombinant vesicular stomatitis virus vaccine expressing Ebola virus glycoprotein that primes the immune system to recognize and attack Ebola virus.

A recombinant vesicular stomatitis virus vaccine expressing Ebola virus glycoprotein that primes the immune system to recognize and attack Ebola virus. Used for Ebola virus disease prevention (marketed as Ervebo).

At a glance

Generic namerVSV∆G-ZEBOV-GP
Also known asErvebo
SponsorUniversity of Birmingham
Drug classLive attenuated viral vector vaccine
TargetZaire ebolavirus glycoprotein (EBOV-GP)
ModalityBiologic
Therapeutic areaImmunology / Infectious Disease
PhaseFDA-approved

Mechanism of action

rVSV∆G-ZEBOV-GP is a live attenuated viral vector vaccine in which the glycoprotein gene of vesicular stomatitis virus (VSV) is replaced with the glycoprotein gene from Zaire ebolavirus (ZEBOV). This allows the vaccine to stimulate both cellular and humoral immune responses against Ebola virus without causing VSV disease. The vaccine triggers production of antibodies and T-cell responses specific to Ebola glycoprotein, providing protection against Ebola virus infection.

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: