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Synergistic Effect of BCL-2 inhibitor Venetoclax with Homoharringtonine on the treatment of Early T-cell Precursor Acute lymphoblastic leukemia and its molecular mechanism

Synergistic Effect of BCL-2 inhibitor Venetoclax with Homoharringtonine on the treatment of Early T-cell Precursor Acute lymphoblastic leukemia and its molecular mechanism

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069069
Enrollment
Unknown
Registered
2023-03-06
Start date
2021-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Early T-cell precursor (ETP) acute lymphoblastic leukemia

Interventions

Experimental group:venetoclax combined with HAG regimen (Venetoclax+HHT+low-dose cytarabin+G-CSF))

Sponsors

The First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age> 14 years old; 2. Cell morphology and immunophenotype are consistent with ETP-ALL diagnosis; 3. The ECOG score is 0-2 points during screening; 4. Expected survival = 2 months; 5. There is no abnormal function of the organs that limit the use of the scheme during the screening period; 6. Understand the research and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with oral medication difficulties or malabsorption syndrome; 2. Diseases with abnormal function of heart, lung, liver, kidney and other organs that may limit patients' participation in this test (including but not limited to serious infection, uncontrollable diabetes, severe cardiac insufficiency or angina, active tuberculosis, asthma, COPD, bronchiectasis, etc.); 3. Cardiac ultrasound LVEF 1.5 ULN (upper limit of normal); ALT or AST or ALP>5ULN; serum creatinine > 1.5 ULN; 6. known HIV infection; 7. Systemic conditions are not suitable for chemotherapy; 8. Unable to understand or follow the research protocol; 9. Subjects receiving potent or intermediate-potency CYP3A inducers/inhibitors within 7 days prior to initiation of study therapy.

Design outcomes

Primary

MeasureTime frame
complete remission;

Secondary

MeasureTime frame
Overall Survival;Event free survival;

Countries

China

Contacts

Public ContactJin Jie

the First Affiliated Hospital, Zhejiang University School of Medicine

jiej0503@zju.edu.cn13505716779

Outcome results

None listed

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