This is a multi-center, open-label, dose escalation study that will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of liposomal annamycin as a single agent for the treatment of subjects with AML that is refractory to or relapsed after induction therapy
Est. Enrollment: 75 participants
Study Start Date: Dec 17, 2018
Study Completion Date: Dec 01, 2022
Age: 18+ years
Gender: All
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