Marion Subklewe, MD, Ludwig-Maximilians-University of Munich, Munich, Germany, discusses the findings and limitations of the Phase I dose-escalation study (NCT04580121), which investigated the safety, tolerability, pharmacokinetics, anti-drug antibodies, and anti-leukemic activity of RO7283420, a bispecific antibody targetting WT1 and CD3 antigens on the surface of acute myeloid leukemia (AML) cells. This interview took place at the 65th ASH Annual Meeting and Exposition, held in San Diego, CA.
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