The FDA has cleared a new antibody drug, that targets the omicron variant, for adults and adolescent patients with mild-to-moderate cases.
But late last month the FDA revoked its emergency use authorization for Regeneron’s antibody drug, along with Lilly’s. The two medications had been the the backbone of antibody treatment, and doctors were hard pressed to come up with fallbacks when they didn’t work against omicron.
Alternate therapies, including antiviral pills from Pfizer and Merck, have been in short supply. An antibody drug from GlaxoSmithKline that remains effective against omicron is also scarce.Under the U.S. contract with Lilly, the government will receive about 300,000 treatment courses of the new antibody drug in February and another 300,000 in March.
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