The U.S. Food and Drug Administration in April revoked the emergency use authorization of Eli Lilly's
(LLY.N) single antibody therapy, bamlanivimab, saying there was increased circulation of variants resistant to the therapy when used alone.
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Other s
tudies have previously shown that some antibody combination therapies remained potent against those emerging variants of the coronavirus that were resistant to single antibody therapies.
The latest study found that combinations of two antibodies often retained potency against variants even when one of the two antibodies lost some or all ability to neutralize the variant in lab studies.
The study, which was conducted in mice and hamsters, tested all single and combination antibody therapies authorized for emergency use by the FDA against emerging international and U.S. variants of the virus.
The researchers evaluated the FDA authorized combination therapies made by Regeneron, Eli Lilly
(LLY.N)and a single antibody therapy, sotrovimab, by Vir Biotechnology Inc
(VIR.O) and GlaxoSmithKline Plc
(GSK.L).