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Monday, May 27, 2024

Sanofi Sarclisa accepted for FDA priority review for multiple myeloma

 

  • FDA Priority Review granted based on positive results from IMROZ phase 3 study

  • If approved, Sarclisa would be the first anti-CD38 therapy in combination with standard-of-care treatment for patients with newly diagnosed transplant-ineligible multiple myeloma

  • Pivotal IMROZ phase 3 study results to be featured during oral presentation at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting

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