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NCT02971397Phase 1Completed
Phase 1, open-label, single-arm trial of cytarabine and daunorubicin in acute myeloid leukemia (AML), sponsored by Wake Forest University Health Sciences. Primary endpoints: Number of Participants With Cardiac Toxicity, Defined as Reduction in LVEF of >= 10% Compared to Baseline LVEF and EF =< 50% on the Follow-up Scan, Assessed Using MRI at 3 months, Unexpected Toxicities (Exclude Hematologic and Infectious) >= Grade 3, as Measured by CTCAE v 4.0 at 30 days and 3 more. Started Nov 2016; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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