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Why Regeneron stopped subscribing to the Anti-Coronavirus Antibody Cocktail study in patients with severe illness



Regeneron Pharmaceuticals Inc (NASDAQ: REGN) faced Friday’s failure in a trial that evaluated its REGN-COV2 antibody cocktail in patients with COVID-1

9 hospitalized.

What happened: An independent data monitoring committee recommended that continued enrollment of patients requiring high-flow oxygen or mechanical ventilation should be halted, citing a potential safety signal and a risk profile. ro-benefits are detrimental at this time, Regeneron said on Friday.

The Committee recommends that admission be continued for hospitalized patients who need low or no oxygen flow, stating that a benefit-risk is acceptable in these groups.

IDMC has sought to make modifications in patient admission trials.

It also suggests that outpatient testing can be conducted without modification.

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Why is it important: Regeneron has an FDA pending emergency use license application for REGN-COV2 in a mild to moderate outpatient coronavirus with a high risk of poor outcome.

Regeneron’s COVID-19 pipeline came to prominence after an investigative antibody cocktail was handed over to President Donald Trump to treat his COVID-19 infection.

Eli Lilly and Co (NYSE: LLY) had to suspend the end-stage study of candidate bamlanivimab antibody therapy in hospitalized severe COVID-19 patients.

REGN price action: At the last check, shares of Regeneron fell 2.49% to $ 541.97.

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