Veklury becomes first option for COVID-19 approved in EU
The European Commission has granted conditional marketing authorization for Veklury (remdesivir) as a treatment for SARS-CoV-2 infection, the virus that causes COVID-19, US biotech Gilead Sciences (Nasdaq: GILD) announced today.
Under this authorization, Veklury is indicated for the treatment of COVID-19 in adults and adolescents (aged 12 years and older and weighing at least 40 kg), with pneumonia requiring supplemental oxygen. The decision comes in just over a week since the European Medicines Agency’s advisory committee said that conditional approval should be granted, and making the drug the first option for the COVID-19 in Europe
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