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FDA Approves Sanofi's Sarclisa (isatuximab) as the 1st Anti-CD38 Therapy in Combination W/ Standard-of-Care Treatment for Adult Patients W/ Newly Diagnosed Multiple Myeloma Not Eligible for Transplant

September 23, 2024 9:17 AM | Katy Monaco (Administrator)

FDA) has approved Sarclisa (isatuximab) in combination with bortezomib, lenalidomide, and dexamethasone (VRd) as a first line treatment option for adult patients with newly diagnosed multiple myeloma (NDMM) who are not eligible for autologous stem cell transplant (ASCT). Sarclisa is the first anti-CD38 therapy in combination with standard-of-care VRd to significantly reduce disease progression or death (by 40%) compared to VRd alone for patients with NDMM not eligible for transplant. Read More.


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