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America Approves Remdesivir To Treat Emegency Coronavirus Patients

American authorities have approved an experimental drug for emergency use on coronavirus patients, as more US states eased pandemic lockdowns despite another spike in deaths from the disease.

The approval is the latest step in a global push to find viable treatments and a vaccine for the coronavirus, which has left half of humanity under some form of lockdown, hammered the world economy, and infected more than 3.3 million people.

Remdesivir, an antiviral drug initially developed to treat Ebola, was given the green light on Friday after a major trial found that it boosted recovery in serious COVID-19 patients. “It’s really a very promising situation,” President Donald Trump said on Friday at the White House, where he was joined by Daniel O’Day, CEO of Gilead Sciences, which developed Remdesivir.

Remdesivir incorporates itself into the virus’s genome, short-circuiting its replication process.

The drug approval came as the US leaders struggled with growing pressure from citizens wearying of stay-at-home orders.

Edafe
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