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Clinical Trial Summary

The purpose of this study is to explore the efficacy and safety of switching to flumatinib versus dasatinib after imatinib-related low-grade adverse events in patients with chronic myeloid leukemia in chronic phase (CML-CP) in China. This is a post-marketing, interventional, double-arm, prospective, open-label, randomized controlled study in CML-CP patients in China. Patients will be recruited consecutively from the study sites during the enrollment period. The enrolled patients will be given flumatinib or dasatinib under the conditions of informed consent and frequent monitoring according to the clinical guideline.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04933526
Study type Interventional
Source Shenzhen Second People's Hospital
Contact Xin Du
Phone 075583366388
Email duxingz@medmail.com.cn
Status Recruiting
Phase Phase 4
Start date July 1, 2021
Completion date June 30, 2023

See also
  Status Clinical Trial Phase
Completed NCT03509896 - Study of Chinese Newly Diagnosed Participants With Philadelphia Chromosome-Positive (Ph+) Chronic Myeloid Leukemia in Chronic Phase (CML-CP)
Terminated NCT00451035 - Efficacy and Safety of LBH589 in Adult Patients With Refractory Chronic Myeloid Leukemia (CML) in Chronic Phase Phase 2
Available NCT04360005 - Managed Access Programs for ABL001, Asciminib