EU regulator recommends Merck’s COVID-19 pill for emergency use
3 years, 1 month ago

EU regulator recommends Merck’s COVID-19 pill for emergency use

Al Jazeera  

The European Union’s medicines watchdog has advised its member states they can use a potentially groundbreaking COVID-19 antiviral pill in emergency situations triggered by soaring infection rates, ahead of the treatment’s formal approval across the bloc. Molnupiravir, which is produced by Merck and Ridgeback Biotherapeutics, can be given within five days of first symptoms to treat adults who do not need oxygen support and are at risk of severe disease, the European Medicines Agency said in a statement on Friday. The EMA said it had issued its advice to support national authorities who may be keen to deploy the pill, to be branded Lagevrio in Europe, ahead of it gaining full authoristation from the regulator “in light of rising rates of infection and deaths due to COVID-19 across the EU”. The UK’s Medicines and Healthcare products Regulatory Agency recommended at the time that the drug be used as soon as possible following a positive COVID-19 test and within five days of the onset of symptoms, citing clinical data.

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