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Monday, August 5, 2019

FDA clears Mustang Bio’s IND for leukemia med

The FDA has approved Mustang Bio’s (NASDAQ:MBIO) IND application to initiate a multi-center Phase 1/2 clinical trial of MB-102 (CD123 CAR T) in acute myeloid leukemia, blastic plasmacytoid dendritic cell neoplasm and high-risk myelodysplastic syndrome.
MB-102 is a CAR T cell therapy that is produced by engineering patient T cells to recognize and eliminate CD123-expressing tumors.

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