Remdesivir close to EU original authorization as COVID-19 treatment, Health News, ET HealthWorld


BRUSSELS: The leader of European Unionmedical agency Guido Rasi on Monday said a first permit for the U.S. pharmaceutical company Gilead‘s remdesivir then to Treatment of covid-19 could be awarded in the coming days.

That European Medicines Agency (EMA) has already recommended compassionate use of remdesivir, which allows a drug to be administered to patients even before it is fully approved.

“A conditional marketing authorization could be issued in the coming days,” Rasi told a hearing in the European Parliament in Brussels.

Apart from remdesivir, Rasi said other possible treatments against COVID-19 that may be readily available are those based on monoclonal antibodies that can “neutralize” the new coronavirus (SARS-CoV-2) that causes COVID-19 disease.

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