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Nurix Therapeutics

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FDA designations

  • European Medicines Agency Grants Orphan Drug Designation to Bexobrutideg for Waldenström MacroglobulinemiaJul 11, 2025

News

  • Nurix Therapeutics enrolls the first patient in a Phase 1b/2 combination study of bexobrutideg in chronic lymphocytic leukemiaOct 7, 2026
  • Nurix Therapeutics announces a second extension of the research term for its oncology program under the Gilead Sciences collaborationOct 5, 2026
  • Nurix Therapeutics presents preclinical data from novel IRAK4 degrader, GS-6791, demonstrating potent inhibition of IL-1 and IL-36 in vitro and efficacy in dermatitis modelSep 17, 2025
  • EMA grants orphan drug designation to Bexobrutideg (NX-5948) for lymphoplasmacytic lymphoma (Waldenström macroglobulinemia)Jul 10, 2025
  • Nurix shows updated data for Bexobrutideg in relapsed/refractory CLL and WM with sustained deepening responsesJun 12, 2025

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