Skip to content

Efficacy and safety of tyrosine kinase inhibitor combined with hypomethylating agent in patients with chronic myeloid leukemia in myeloid blast phase (acute myeloid leukemia): A prospective, observational single arm study

Efficacy and safety of tyrosine kinase inhibitor combined with hypomethylating agent in patients with chronic myeloid leukemia in myeloid blast phase (acute myeloid leukemia): A prospective, observational single arm study - Tyrosine kinase inhibitor combined with hypomethylating agent in patients with chronic myeloid leukemia in myeloid blast phase (acute myeloid leukemia)

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055887
Enrollment
Unknown
Registered
2022-01-22
Start date
2021-06-01
Completion date
Unknown
Last updated
2023-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic myeloid leukemia in myeloid blast phase (acute myeloid leukemia)

Interventions

Tyrosine kinase inhibitor combined with hypomethylating agent group:None

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged 18 years and over; 2.Chronic myeloid leukemia in myeloid blast phase resistant or intolerant to at least one type of TKI; 3.No severe dysfunction of heart, lung, liver or kidney; 4.Be able to understand and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Subjects with a history of severe cardiological or cerebral disease; 2. Subjects who have received allogeneic hematopoietic stem cell transplantation; 3. Severe uncontrollable infection; 4. Subjects known to be allergic to the drug used in this study; 5. Pregnant or lactating female, or Subjects with a pregnancy plan during the study.

Design outcomes

Primary

MeasureTime frame
Major hematologic response;

Secondary

MeasureTime frame
Complete hematologic response;Major cytogenetic response;Major cytogenetic response;Progression free survival;Overall survival;

Countries

China

Contacts

Public ContactJiang Qian

Peking University People's Hospital

jiangqian@medmail.com.cn+86 13611115100

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026