- Following recommendations from the Independent Data Monitoring Committee (IDMC), Regeneron Pharmaceuticals Inc (NASDAQ: REGN) will make changes to the Phase 3 trial evaluating REGEN-COV (casirivimab with imdevimab) in outpatients with COVID-19.
- The company said that an independent panel found the company's COVID-19 antibody cocktail at both 1,200mg and 2,400mg doses have "clear clinical efficacy" in reducing the rates of hospitalization and deaths in patients.
- The panel has recommended that Regeneron should stop enrolling patients in the placebo group.
- The cocktail was authorized in November for emergency use by the FDA.
- The company plans to share details of unblinded data from the trial once it becomes available in March.
- Price Action: REGN is marginally up by 0.5% at $460.9 in premarket trading on the last check Thursday.
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