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Clinical Trial Summary

The purpose of this study is to explore the efficacy and safety of flumatinib in chronic phase of chronic myeloid leukemia (CML-CP) patients With Ph+ post imatinib failure.


Clinical Trial Description

A multicenter, single-arm, prospective, open-label study to detect the efficacy and safety of flumatinib by measuring rates of major molecular response (MMR) at 12 months in CML-CP patients with Ph+ in China. Approximately 200 Patients will be recruited consecutively from the study sites during the enrollment period and will be given flumatinib 600 mg QD. The duration of patient participation will be 24 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04677439
Study type Interventional
Source Shenzhen Second People's Hospital
Contact Xin Du, Phd
Phone 075583366388
Email duxingz@medmail.com.cn
Status Recruiting
Phase Phase 4
Start date January 1, 2021
Completion date December 30, 2023

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