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Clinical study of dasatinb in maintenance chemotherapy for adult acute myeloid leukemia (not acute promyelocytic leukemia)

Observational study of dasatinb in maintenance chemotherapy for adult acute myeloid leukemia (not acute promyelocytic leukemia)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17012278
Enrollment
Unknown
Registered
2017-08-07
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

acute myeloid leukemia

Interventions

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Diagnosed with AML(not APL);To be aged 18~65 years; Liver and renal function: serum bilirubin<=35umol/L, AST/ALT lower than 2* upper normal serum level, creatinine<=150umol/L; Normal cardiac function: NYHA I/II; Performance status: Eastern Cooperative Oncology Group (ECOG) 0-2; Non-pregnant and non-nursing; Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test to rule out pregnancy; Women of child-bearing potential must either commit to take birth control measures at least four weeks before she begins dasatinib therapy; Men must agree not to father a child and must use a latex condom during any sexual contact with women of childbearing potential while taking dasatinib and for 3 months after therapy is stopped; Signed written informed consent.

Exclusion criteria

Exclusion criteria: APL; Liver and renal insufficiency (beyond the inclusion criteria); Patients with ejection fraction 2); Patients with a "currently active" second malignancy; Patients with "currently active" tuberculosis. Patients with HIV;active HBV, HCV, or Hepatitis A infection; Patients who can't understand or obey the protocol; atients participated in other clinical trial; Other circumstance that obstructs the clinical trial.

Design outcomes

Primary

MeasureTime frame
Event Free Survival;Overall survival;recurrence rate;

Secondary

MeasureTime frame
Death Rate;Toxicity and Safety;

Countries

China

Contacts

Public ContactShifeng Lou

The Second Affiliated Hospital of Chongqing Medical University

13508331213@163.com+86 13508331213

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026