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China Children's Leukemia Group (CCLG) - AML2019 supplementary study on pediatric acute myeloid leukemia -Venetoclax therapy

China Children's Leukemia Group (CCLG) - AML2019 supplementary study on pediatric acute myeloid leukemia - Venetoclax therapy - CCLG-AML 2019- Venetoclax targeted therapy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058925
Enrollment
Unknown
Registered
2022-04-20
Start date
2022-04-15
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 (AML)

Interventions

Intolerant to chemotherapy group:venetocax
Refractory or relapse group:venetocax
Genetically poor prognosis group:venetocax
t-AML group:venetocax

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 enrolled in China Children's Leukemia Group (CCLG) - AML2019 study; 2. Patients who are intolerant to chemotherapy; 3. Patients who do not remit from induction therapy, or who have persistently positive MRD after treatment, or whose MRD turn negative and then turn positive again or who have morphological relapse; 4. Patients who have genetic markers of poor prognosis; 5. Patients who have AML induced by chemotherapy/radiotherapy, or who have AML transformed from myelodysplastic syndrome (MDS).

Exclusion criteria

Exclusion criteria: 1. Acute promyelocytic leukemia (APL); 2. Juvenile monocytic leukemia (JMML); 3. Only temporary chemotherapy, radiotherapy or immunotherapy, rather than systematic treatment according to the treatment plan; 4. Had received any antitumor therapy within 2 weeks prior to enrollment, except single dose sheath injection and hydroxy uria or low dose cytarabine for hyperleukaemia; 5. Any comorbidities or mental illnesses with significant abnormalities that affect patient life safety and compliance, informed consent, study participation, follow-up, or interpretation of results.

Design outcomes

Primary

MeasureTime frame
Remission State of Bone Marrow;Minimal Residual Disease;Side Effect of Chemotherapy;

Countries

China

Contacts

Public ContactZheng Huyong
zhenghuyong@vip.sina.com+86 10 59617621

Outcome results

None listed

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