The European Commission has granted a conditional marketing authorization to Merck Sharp & Dohme Ltd.’s Ervebo vaccine to protect individuals aged 18 and over from Ebola caused by Zaire ebolavirus strains. The product is the first Ebola vaccine to gain regulatory approval.
Merck’s Ervebo Becomes World’s First Approved Ebola Vaccine
European Commission Grants Conditional Approval
Merck Sharp & Dohme will begin manufacturing licensed doses of Ervebo in Germany and will continue to send investigational vaccine doses to Democratic Republic of Congo.

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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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