Merck and Ridgeback Biotherapeutics announced that the Committee for Medicinal Products for Human Use of the European Medicines Agency has recommended the refusal of the marketing authorization for lagevrio for the treatment of certain adults who have been diagnosed with COVID-19 in the European Union. Merck and Ridgeback will appeal the decision and request a re-examination of the CHMP’s opinion.
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Published first on TheFly
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