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EU regulator starts evaluating COVID-19 drug Ronapreve

European Medicines Agency expected to decide in two months if drug to prevent, treat COVID-19 can be marketed in EU

Agnes Szucs   | 12.10.2021
EU regulator starts evaluating COVID-19 drug Ronapreve


The European Medicines Agency (EMA) began Monday to evaluate whether the COVID-19 drug Ronapreve can be marketed in the European Union, the EU’s main drug regulator announced. 

The medicine, co-developed by US-based Regeneron Pharmaceuticals and the Swiss pharma company Roche, is meant to treat and prevent COVID-19 in people over 12 years of age.

“The EMA will assess the benefits and risks of Ronapreve under a reduced timeline and could issue an opinion within two months,” it said, explaining that they have already done a pre-assessment called a rolling review based on data from laboratory and animal studies as well as clinical trials.

The drug is made of a combination of two monoclonal antibodies, casirivimab and imdevimab, which were designed to recognize and attach to the spike protein of the COVID-19 virus.

Patients can receive Ronapreve by infusion into a vein or by injection under the skin.

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