Pfizer Inc. has snagged a conditional marketing authorization (CMA) from the European Commission (EC) for Paxlovid (nirmatrelvir and ritonavir), for patients with COVID-19 who do not require supplemental oxygen and are at increased risk of progressing to severe disease. The decision came just a day after the Committee for Medicinal Products for Human Use (CHMP) issued a positive opinion on the drug. (Also see "EU Approves Paxlovid For COVID-19" - Pink Sheet, 27 January, 2022.)
The CMA follows by about a month the 22 December US Food and Drug Administration’s emergency use authorization for the...








