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FDA approved Eli Lilly COVID treatment for emergency use

The Food and Drug Administration has given emergency approval for the use of an experimental antibody treatment from Eli Lilly to treat people with COVID-19, Business Insider reports.

The treatment is similar to a Regeneron antibody cocktail received by Donald Trump when he was hospitalized at Walter Reed Military Medical Center in Bethesda Maryland in early October.

The treatment is not a cure.  It’s a therapy that lowers viral loads in patients with mild to moderate cases of COVID-19, reducing the risk of the infection worsening.  It has shown no significant side effects in patients.

The emergency approval allows medical providers to give the treatment to high-risk coronavirus patients.

Last month, Eli Lilly CEO David Ricks said the company wanted patients to have “no or very, very low out-of-pocket costs anywhere in the world to receive this therapy.”

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