Skip to content

A prospective, single-arm, multi-center clinical study to evaluate the efficacy and safety of Olverembatinib combined with VP regimen in the treatment of newly diagnosed Ph-positive acute lymphoblastic leukemia

A prospective, single-arm, multi-center clinical study to evaluate the efficacy and safety of Olverembatinib combined with VP regimen in the treatment of newly diagnosed Ph-positive acute lymphoblastic leukemia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059850
Enrollment
Unknown
Registered
2022-05-13
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Ph-positive acute lymphoblastic leukemia

Interventions

Understand and voluntarily sign an informed consent form:Olverembatinib with vindesine and prednisolone

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed philadelphia chromosome-positive acute lymphoblastic leukemia; 2. Aged >= 18 years; 3. Healthy liver and kidney function (creatinine <= 1.5 * ULN, BUN <= 1.5 * ULN, ALT <= 3 * ULN, AST <= 3 * ULN, Total bilirubin <= 3 * ULN); 4. Understand and comply with all test protocol requirements; 5. Accept oral medicine,Understand and voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. CML-BP; 2. Can not come back for eximination on time;Can not understand and voluntarily sign an informed consent form.

Design outcomes

Primary

MeasureTime frame
Complete molecular remission;

Secondary

MeasureTime frame
Overall response Rate (CR+CRi);Overall survival;Minimal Residul disease;Major Molecualr remission;

Countries

China

Contacts

Public ContactJin Jie

The First Afflilated Hospital, Zhejiang University School of Medicine

jiej0503@163.com+86 13505716779

Outcome results

None listed

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