Sanofi says FDA approves Sarclisa Escena subcutaneous formulation for multiple myeloma treatment in US

  • FDA cleared Sanofi’s Sarclisa Escena, a subcutaneous isatuximab formulation, for multiple myeloma across all existing Sarclisa IV indications.
  • Product becomes the first anticancer therapy in the US administered via an on-body injector, using Enable Injections’ CirCLIQ device.
  • Phase 3 IRAKLIA study showed non-inferior response rates versus IV Sarclisa, with fewer systemic administration reactions.


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