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Clinical study of azacytidine combined with low-dose venetoclax in the treatment of untreated fragile senile AML

Clinical study of azacytidine combined with low-dose venetoclax in the treatment of untreated fragile senile AML

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050154
Enrollment
Unknown
Registered
2021-08-19
Start date
2021-09-15
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

acute myeloid leukemia

Interventions

Eexperimental group:Azacytidine plus low dose venetoclax

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged at least 60 years; 2. Patients diagnosed as AML (not APL); 3. Previously untreated; 4. No uncontrolled current infection (new infection, broad spectrum antibiotics, body temperature greater than 38? within 72 hours, excluding other non-infectious factors); 5. The patients themselves or their family members are willing to participate in the study and sign an informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiopulmonary or other important organ dysfunction; 2. Patients who cannot comprehend or follow the plan with a brain disorder or serious mental diseases; 3. Patients combined with other malignant tumors; 4. Patients with CNSL involvement; 5. Patients whose necessary treatment plan and follow-up observation cannot be guaranteed.

Design outcomes

Primary

MeasureTime frame
Complete remission;Complete remission with incomplete blood count recovery;Overall survival;

Secondary

MeasureTime frame
Time to response;Duration of response;Rates of death;Relapse rate;

Countries

China

Contacts

Public ContactLiu Hui

Beijing Hospital

liuhui8140@126.com+86 13520618812

Outcome results

None listed

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