This is a multi-center open clinical study aimed at evaluating the efficacy and safety of Clifutinib Besylate combined with chemotherapy in newly-treated adult subjects with AML
Main purpose:To evaluate the tolerability and safety of Clifutinib Besylate combined with DA (Cytarabine + Daunorubicin) or AZA (Azacitidine) in newly-treated adult AML subjects; explore reasonable therapeutic doses through climbing tests in different dose groups. To evaluate the efficacy of Clifutinib Besylate combined with DA or AZA in newly treated adult AML subjects. Secondary purpose:To observe the pharmacokinetic (PK) characteristics of Clifutinib combined with DA or AZA in newly-treated adult AML subjects and the drug interaction between Clifutinib and AZA at the same time.Observe the correlation of different subtypes and prognostic risk with the efficacy of Clifutinib and the changes of genes before and after treatment.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
133
The queue 1 is divided into Induction therapy and Consolidation therapy and Maintenance treatment The queue 2 will receive oral Clifutinib Besylate once daily until disease progression or unacceptable toxicity occurs
the First Affiliated Hospital,College of Medicine,Zhejiang University
Hanzhou, Zhejiang, China
RECRUITINGMaximum tolerated dose(MTD)
Safety and Tolerability assessed through adverse events to determine maximum tolerated dose
Time frame: day 1-28
Composite CR rate
CR + CRi +CRMRD-
Time frame: Up to 12 months
Duration of response
The time from receive CR / CRi/CRMRD-/PR to relapse
Time frame: up to 12 months
Objective response rate
CR + CRi +CRMRD- + PR
Time frame: up to 12 months
Event Free Survival
From the first time taking experimental drug to treatment failure or progression or relapse or death
Time frame: up to 12 months
Overall Survival
From the first time taking experimental drug to death
Time frame: up to 12 months
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