The European Commission made the rare decision Monday not to adopt the negative opinion of the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) on the renewal of Translarna’s conditional authorization.
The EC sent the opinion back to the CHMP for further evaluation, allowing the Duchenne muscular dystrophy therapeutic to remain on the market for now. PTC Therapeutics wrote that the EC “asked the CHMP to further consider the totality of evidence, including data from patient registries and real-world evidence, in a revised opinion.”
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