Merck (MRK), Ridgeback Biotherapeutics Provide Update on Results from MOVe-OUT Study of Molnupiravir, an Investigational Oral Antiviral Medicine, in At Risk Adults With Mild-to-Moderate COVID-19

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Merck (MRK) and Eisai Announces EU Approval of LENVIMA Plus KEYTRUDA as First-Line Treatment for Adult Patients With Advanced Renal Cell Carcinoma

November 29, 2021 5:52 AM EST

Eisai and Merck & Co., Inc., Kenilworth, N.J., U.S.A. (NYSE: MRK) today announced that the European Commission has approved the combination of LENVIMA (KISPLYX in the European Union [EU] for the treatment of advanced renal cell carcinoma [RCC]), the orally available multiple receptor... More

FDA posts briefing documents on Merck (MRK) /Ridgeback antiviral molnupiravir

November 26, 2021 9:07 AM EST

FDA posts briefing documents on Merck (NYSE: MRK) /Ridgeback antiviral molnupiravir

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