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U.S FDA Approves Merck Ebola vaccine

The U.S. Food and Drug Administration said on Thursday it approved drugmaker Merck & Co’s (MRK.N) Ebola vaccine Ervebo, making it the first FDA-authorised vaccine against the deadly virus.

The vaccine was used by the World Health Organization and Democratic Republic of the Congo as an investigational vaccine to help reduce Ebola virus disease (EVD) outbreaks in few West African countries from 2014 to 2016.

Uganda also used the vaccine manufactured by Merck, was used effectively at the end of the 2013-2016 outbreak in the DRC and has been used during the current epidemic. Over 180,000 people have received this vaccine by August 2019.

The Ebola virus, which causes haemorrhagic fever and spreads from person to person through direct contact with body fluids, has killed more than 2,100 people in Congo since the middle of the year, making it the second-largest Ebola outbreak in history.


However the supply is sporadic, and vaccine administrators are typically 1,000 doses short of what they need, according to Doctors Without Borders as reported by Bloomberg News.

The vaccine, which is administered as a single-dose injection, will help to prevent EVD caused by Zaire ebolavirus in patients aged 18 years and older, the regulator said in a statement. The Merck vaccine is administered through one shot and takes 10 days to be effective

Merck welcomed the FDA’s decision, describing it as an important milestone in the fight against the deadly virus.

In November, Merck received approval from the European Commission to market Ervebo, less than a month after a European medicines panel backed the first-ever vaccine against the virus.


Written by How Africa

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