Gilead stopped a Phase III study of its CD47 antibody magrolimab in patients who have acute myeloid leukemia with TP53 mutations, the company announced Tuesday.
In a press statement, the company said, “Based on an ad hoc analysis, and following review by an independent data monitoring committee, Gilead concluded that magrolimab is unlikely to demonstrate a survival benefit in AML with TP53 mutations compared to standard of care.”
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