Remdesivir Recommended for EU Authorization as First COVID-19 Treatment
• The European Medicines Agency (EMA) has recommended Remdesivir for authorization in the EU, marking it as the first COVID-19 treatment to receive such a recommendation. • The CHMP recommends Remdesivir be used in adults and adolescents (12+) with pneumonia requiring supplemental oxygen. • A study showed Remdesivir-treated patients recovered in 11 days versus 15 days with a placebo, a 31% faster recovery. • Remdesivir, initially developed for Ebola, interferes with RNA virus replication and has shown success against coronaviruses in lab studies.

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EMA recommends Remdesivir for COVID-19 treatment in EU; CHMP to test in adults/adolescents with pneumonia requiring oxyg...