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EMA Reviewing Two MAb Combinations For COVID-19

Products Being Assessed Under Special Procedure For EU Member States

 
• By Ian Schofield

The European Medicines Agency's special review process that was used to help EU member states issue emergency use approvals for dexamethasone in COVID-19 patients is now being applied to two antibody combinations from Regeneron/Roche and Lilly.

European Union flag with covid-19 coronavirus in background
More products for use in COVID-19 are being assessed in Europe • Source: Shutterstock

The European Medicines Agency is carrying out a review of two monoclonal antibody combinations with potential in treating COVID-19, under a special procedure that assists the EU member states in making medicinal products available in emergency situations before they have been formally approved.

The two combinations in question are casirivimab/imdevimab and bamlanivimab/etesevimab. The first is being co-developed as REGN-COV2 by 

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