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Merck Will Apply for EUA of COVID-19 Antiviral in Wake of Promising Phase III Data

An interim analysis of data from 775 patients in the Phase III portion of the MOVe-OUT trial showed that 28 of 385 patients (7.3%) who received molnupiravir were either hospitalized or died through Day 29 following randomization, compared with 53 of 377 patients (14.1%) treated with placebo.
Dainam Graybosch Ridgeback Biotherapeutics Robertm Davis Michael Yee Merck Co Data Monitoring Committee

Merck COVID-19 pill success slams Moderna shares, shakes up healthcare sector

Positive clinical trial results for Merck & Co's experimental antiviral COVID-19 pill reverberated through the healthcare sector on Friday, sending the drugmaker's stock price soaring while denting high-flying shares of vaccine companies and makers of other coronavirus therapies.
New York United States Manojna Maddipatla Bahl Gaynor Sahak Manuelian Piper Sandler

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Merck to Seek FDA EUA for COVID-19 Pill after Positive Phase III Data

Merck & Co., said today it will pursue FDA emergency use authorization (EUA) “as soon as possible” for molnupiravir, the COVID-19 oral antiviral candidate it is developing with Ridgeback Biotherapeutics, following Phase III data showing an approximately 50% reduction in the risk of hospitalization or death in patients 29 days after treatment with the pill.
Dainam Graybosch Ridgeback Biotherapeutics Robertm Davis Michael Yee Merck Co Data Monitoring Committee

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