Coronavirus Update: Gilead's Veklury Gets Full FDA Approval, Roche Partners With Atea

Moderna Fully Enrolls COVE Trial

Gilead's remdesivir is first drug fully approved by FDA to treat COVID-19. Roche and Atea team up on an investigational direct acting antiviral while Moderna reaches the 30,000-patient enrollment target for its Phase III COVE study of the company's investigational mRNA vaccine.   

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Gilead Sciences, Inc.'s Veklury (remdesivir) is the first and only drug approved by the US Food and Drug Administration for the treatment of COVID-19, although it is already widely used for treating the infection in hospitalized patients. Veklury was granted an emergency use authorization in May for the treatment of patients with COVID-19 requiring hospitalization. (Also see "Gilead Sets Remdesivir Price, Commits Nearly All Near-Term Supplies To US" - Scrip, 30 June, 2020.)

The antiviral was one of the first options to become available to patients hospitalized with COVID-19, along with the steroid dexamethasone. While supply was constrained initially, Gilead has ramped up the manufacturing capacity for Veklury

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