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CLINICAL TRIALS
Study of Liposomal Annamycin for the Treatment of Subjects With Acute Myeloid Leukemia (AML)
Active, not recruiting
Study of Liposomal Annamycin for the Treatment of Subjects With Acute Myeloid Leukemia (AML)
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
info
The number of participants in a clinical study. The "estimated" enrollment is the
target number of participants the researchers need for the study.
Study Start Date: Dec 17, 2018
info
These are the dates the researchers think the study will start and end.
Study Completion Date: Dec 01, 2022
info
The "estimated" study completion date is the date the researchers think the last
participant in a clinical study was examined or received an intervention/treatment. This
is also the expected date that the study will be completed
Age: 18+ years
Gender: All
Study Description
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Study Details
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