Skip to content

Study for the role of pegaspargase, cyclophosphamide, demethyl daunorubicin, vindesine and dexamethasone in inducion remission of adults Ph negative acute lymphoblastic leukemia

Role of pegaspargase, cyclophosphamide, demethyl daunorubicin, vindesine and dexamethasone in inducion remission of adults Ph negative acute lymphoblastic leukemia: A prospective, open-lable, randomized controlled study.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023805
Enrollment
Unknown
Registered
2019-06-12
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

Adults Ph negative acute lymphoblastic leukemia

Interventions

Exeprimental group:Protocol of pegaspargase, cyclophosphamide, demethyl daunorubicin, vindesine and dexamethasone
Control group:Protocol of pegaspargase, cyclophosphamide, daunorubicin, vindesine and dexamethasone

Sponsors

Medical Center of Hematology, Xinqiao Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Understand and voluntarily sign an informed consent form. 2. Male or femal with age from 14 to 70 years 3. Newly diagnosed Ph negative acute lymphoblastic leukemia 4. The estimated survival is over three months 5. Adequate main organ function: (1) Liver: ALT/AST 40 %. 6. Karnofsky =60 at study entry

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding female subject; 2. Drug abusers; 3. uncontrolled infection 4 weeks before enrolled; 4. Known positive for HIV or acute infectious hepatitis, type A, B or C; 5. other primary tumor except for ALL; 6. Serious autoimmune disease or mmune deficiency disorder; 7. Central nervous involvement; 8. Serious psychiatric or psychological disorders; 9. Patients can not be enrolled judged by the researchers.

Design outcomes

Primary

MeasureTime frame
Rate of minimal residual disease negativity;

Secondary

MeasureTime frame
Rate of complete remission;

Countries

China

Contacts

Public ContactXi Zhang

Medical Center of Hematology, Xinqiao Hospital of Army Medical University

zhangxxi@sina.com+86 023-68755609

Outcome results

None listed

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