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EMA Panel Recommends Expanded Use of Merck’s Enflonsia in Europe

The Committee for Medicinal Products for Human Use backed a broader indication for the RSV prevention treatment, whose active ingredient is clesrovimab.

A medicine vial sits alone on a long review table / TokenPost.ai
A medicine vial sits alone on a long review table / TokenPost.ai

The Committee for Medicinal Products for Human Use, part of the European Medicines Agency (EMA), recommended approval of an expanded indication for Merck’s Enflonsia (clesrovimab), an RSV prevention treatment.

The endorsement moves the proposed change through the European review process toward approval.

Riza Dagoc

Riza Dagoc reports on regulation, investing and the digital-asset business for TokenPost. Send corrections or tips to info@tokenpost.com.

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