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Approval is based on GMMG-HD7 phase 3 study for those who are transplant-eligible, newly diagnosed with multiple myeloma.
July 25, 2025
By: Rachel Klemovitch
Assistant Editor
The European Commission has approved Sanofi’s Sarclisa in combination with bortezomib, lenalidomide, and dexamethasone (VRd) for the induction treatment of adult patients with newly diagnosed multiple myeloma (NDMM) who are eligible for autologous stem cell transplant. This follows the positive opinion of the European Medicines Agency’s Committee for Medicinal Products for Human Use on June 19, 2025. The approval is based on results from part one of the two-part, double-r...
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