This is a Phase 2, open-label, multicenter study to safety \& tolerability, antitumor activity, and pharmacokinetics of FCN-338 in Combination with szacitidine (AZA) or chemotherapy(erythromycin, cytarabine(Ara-C)) in Patients with myeloid neoplasms
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Incidence of DLT
Timeframe: At the end of Cycle 1 (each cycle is 28 days)
Title: composite CR rate (CRc)
Timeframe: From the first dose to the end of maintenance phase, assessed up to 30 months
Minimal residual disease (MRD) negative rate
Timeframe: From the first dose to the end of maintenance phase, assessed up to 30 months