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Thursday, September 16, 2021

Intellia: FDA accepts application for leukemia med

 

  • NTLA-5001 is Intellia’s first ex vivo candidate using its proprietary cell engineering process for the treatment of cancer to enter clinical study

  • NTLA-5001 targets Wilms’ Tumor 1 (WT1), an overexpressed intracellular antigen on many hematologic malignancies and solid tumors

  • Initiation of patient screening in Phase 1/2a study of NTLA-5001 expected by year-end

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