EU approves remdesivir vs Covid-19

BRUXELLES: The European Commission, the European Union’s executive arm, on Friday (Saturday in Manila) authorized the use of antiviral drug remdesivir to treat the coronavirus disease 2019 (Covid-19).

“Today’s authorization of a first medicine to treat Covid-19 is an important step forward in the fight against this virus,” EU Health Commissioner Stella Kyriakides said in a statement.

“We are granting this authorization less than a month after the application was submitted, showing clearly the EU’s determination to respond quickly whenever new treatments become available,” she said.

At least two major United States studies have shown that remdesivir can reduce the duration of hospital stays for Covid-19 patients.

Washington authorized the emergency use of the medicine — which was originally intended as a treatment for Ebola — on May 1, followed by several Asian nations including Japan and South Korea.

The green light comes on the recommendation of the European Medicines Agency, which gave its conditional authorization last week for the treatment of patients above 12 years of age who are suffering pneumonia and require extra oxygen.

To stay updated on news, advisories, and explainers, check out our special coverage page, “Novel Coronavirus Outbreak.” It said its assessment was based mainly based on data from a study sponsored by the US National Institute of Allergy and Infectious Diseases.

The research, published in the leading journal the NewEngland in May, showed that injections of remdesivir speeded patient recovery compared with a placebo.

On average it reduced patients’ hospital stays from 15 days to 11.