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MP 0420 filed with FDA for EUA in COVID-19

Read time: 1 mins
Published:11th Feb 2022

Molecular Partners was informed by Novartis that the company has requested Emergency Use Authorization (EUA) from the FDA for MP 0420 (ensovibep), a DARPin antiviral therapeutic candidate to treat COVID-19.

This submission is based on the totality of the data from clinical and preclinical studies including the positive results of the Phase II portion of the EMPATHY study, a randomized, placebo-controlled study which enrolled 407 symptomatic patients infected with SARS-Cov-2.

Condition: Coronavirus/COVID-19 Infection
Type: drug

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