Collaboration builds on the groundbreaking research of Columbia University oncologist Dr. Siddhartha Mukherjee that uses gene-editing to remove the CD33 surface protein from hematopoietic stem cells
- Actimab-A to be used post-transplant of these engineered stem cells to prevent relapse by selectively targeting residual CD33 positive leukemia cells while sparing the engineered stem cells
- High rates of measurable residual disease negativity demonstrated by Actimab-A + CLAG-M validates merits of Actimab-A's use to prevent disease relapse post gene edited stem cell transplant
- Actimab-A + CLAG-M data to be presented in oral presentation at American Society of Hematology Annual Meeting on Saturday, December 10th highlighting 53% 1-year and 32% 2-year overall survival, 67% Overall Response Rate and 72% MRD negativity in patients with relapsed or refractory acute myeloid leukemia
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