Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05564650Phase 1Completed
Phase 1, open-label, single-arm trial of navitoclax in myelodysplastic syndrome (MDS), sponsored by Thomas Jefferson University. Primary endpoints: Maximally Tolerated Dose of Navitoclax in Combination with Venetoclax and Decitabine at 30 days and Complete Response Rate at 4 months. Started Jan 2023; 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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