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Multicenter clinical study of CCLG-AML2024 protocol (except APL)

Multicenter clinical study of CCLG-AML2024 protocol (except APL)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080307
Enrollment
Unknown
Registered
2024-01-25
Start date
2024-01-31
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

Acute myeloid leukemia in children

Interventions

Venetoclax+CRNIT GROUP:The combination of targeted therapy and chemotherapy was applied in the treatment of reduction of volume, induction therapy, consolidation therapy and maintenance therapy, and v
Venetoclax GROUP:The combination of targeted therapy and chemotherapy was applied in the treatment of reduction of volume, induction therapy, consolidation therapy and maintenance therapy, and only Ve

Sponsors

Beijing Children's Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed of AML; 2. Patients younger than 18 years old; 3. Patients who haven't received pre-treatment, except for those who receive single IT injection or Hydroxycarbamide or low-dose Ara-c for Leukocytosis (no more than 300mg/m2); 4. Patients or/and their guardian who have signed the Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1. Junior Myelomonocytic Leukemia; 2. Mixed Phenotype Acute Leukemia; 3. Acute Promyelocytic Leukemia; 4. Patients who received any anti-tumor treatment within 2 weeks, except for those who received single IT injection or Hydroxycarbamide or low-dose Ara-c for Leukocytosis; 5. Patients complicated with any other diseases or psychiatric disease that could affect their safety and compliance, informed consent, participation, follow-up or interpretation of results.

Design outcomes

Primary

MeasureTime frame
OS;EFS;DFS;Complete response rate after induction therapy;MCR rate after induction therapy;

Secondary

MeasureTime frame
Time to complete remission after treatment;Time to MCR after treatment;

Countries

China

Contacts

Public ContactZheng huyong

Beijing Children's Hospital, Capital Medical University

zhenghuyong@vip.sina.com+86 133 7011 5036

Outcome results

None listed

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