Merck’s ERVEBO® [Ebola Zaire Vaccine (rVSVΔG-ZEBOV-GP) live] Granted Conditional Approval in the European Union
Retrieved on:
Monday, November 11, 2019
The approval is based on data submitted to the European Medicines Agency for accelerated assessment in March 2019.
Key Points:
- The approval is based on data submitted to the European Medicines Agency for accelerated assessment in March 2019.
- ERVEBO is currently under Priority Review with the U.S. Food and Drug Administration (FDA) with a target action date of March 14, 2020.
- The European Commissions marketing authorization of ERVEBO is the result of an unprecedented collaboration for which the entire world should be proud.
- After recognizing the need and urgency for an Ebola Zaire vaccine, many came together across sectors to answer the global call for outbreak preparedness.