EU regulator backs Sanofi's injectable version of blood cancer drug

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The European Medicines Agency has recommended the approval of Sanofi’s injectable version of its blood cancer drug, Sarclisa, administered via an on-body injector. This subcutaneous formulation demonstrated non-inferiority to the intravenous version in late-stage trials. The European Commission is expected to make a final decision on approval in the coming months, which could simplify treatment for patients with multiple myeloma.

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