Actively Recruiting

Phase 1
Phase 2
Age: 15Years +
All Genders
NCT06757855

Olverembatinib Combined With Venetoclax and Azacitidine in Blast Phase Ph Chromosome-positive CML

Led by Institute of Hematology & Blood Diseases Hospital, China · Updated on 2025-05-30

29

Participants Needed

1

Research Sites

200 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Even in the TKI era, the outcoms of patients with blast phase is still poor.The response rate to conventional intensive chemotherapy is only 12.5% and the 5-year survival rate is 0 for patients with myeloid blast crsis. The response rate of TKI monotherapy is about 50% and the response rate is further improved when combined TKI and chemotherapy for patients with lymphoid blast crsis. The induction remission rate of chemotherapy alone for patients with Ph-positive acute lymphoblastic leukemia is 50-60%, and the remission rate increases to more than 95% when combined with TKI. Therefore, the application of TKI for patients in the blast crisis phase is of great significance. Olverembatinib is the only third-generation TKI drug approved in the Chinese mainland at present. Preclinical research data show that olverembatinib has a significant inhibitory effect on wild-type and mutant ABL resistant to the first and second-generation TKIs, as well as some complex mutations resistant to ponatinib. Phase I and II clinical studies have shown that for CML patients in the chronic and accelerated phases with resistance or intolerance to various TKIs, with or without T315I mutations, there are significant hematological and molecular responses and survival benefits. Olverembatinib can also inhibit many other kinases related to tumors. In vitro studies have shown that olverembatinib downregulates MCL-1 expression and acts synergistically with BCL-2 inhibitors to induce apoptosis of AML cells. Preclinical studies have shown that venetoclax has a synergistic effect with TKIs. It upregulates apoptosis-inducing proteins, downregulates anti-apoptotic protein MCL1, inhibits the anti-apoptotic activity of BCL-XL, induces apoptosis of Ph+ cells, overcomes TKI resistance, and eliminates CML leukemia stem cells. A large amount of evidence indicates that DNA hypermethylation plays an important role in the progression of CML, and abnormal DNA methylation is associated with progression to the accelerated and blast crisis phases and resistance to TKIs.Domestic scholars have reported successful cases of combined treatment with TKI, venetoclax, and demethylating agent azacitidine for CML patients with lymphoid blast crisis. Therefore, we designed this study to explore the efficacy and safety of olverembatinib, venetoclax, and azacitidine in the treatment of CML patients in the blast crisis phase.

CONDITIONS

Official Title

Olverembatinib Combined With Venetoclax and Azacitidine in Blast Phase Ph Chromosome-positive CML

Who Can Participate

Age: 15Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 15 years or older with t(9;22)(q34;q11)/BCR::ABL1 positive blast-phase chronic myeloid leukemia
  • Blast phase defined by 2022 WHO criteria: bone marrow or blood blasts 60 20%; or immature lymphoblasts 60 5% for lymphoid transformation
  • ECOG performance status score of 2 or less
  • Adequate major organ function including bilirubin < 1.5�d7 upper limit of normal, AST and ALT 60 2.5�d7 ULN, creatinine < 2�d7 ULN, myocardial enzymes < 2�d7 ULN, serum amylase 60 1.5�d7 ULN
  • Normal left ventricular ejection fraction on echocardiography
  • Men and women of reproductive potential agree to use effective contraception
  • Signed informed consent by patient or legal guardian
Not Eligible

You will not qualify if you...

  • Prior systemic anti-cancer treatments for acute transformation, except single-agent TKI, hormone, hydroxyurea, or short-term olverembatinib 60 14 days
  • Myocardial infarction within 12 months or significant cardiac diseases like unstable angina, heart failure, uncontrolled hypertension, or arrhythmias
  • Uncontrolled active severe infection
  • Known positive HIV test
  • Acute pancreatitis within 1 year or history of chronic pancreatitis
  • Uncontrolled hypertriglyceridemia (triglycerides > 450 mg/dL) or hypercholesterolemia (total cholesterol 60 6.2 mmol/L)
  • Another malignancy treated within 5 years or residual disease, except completely resected non-melanoma skin cancer or carcinoma in situ
  • Pregnant or breastfeeding women
  • CNS leukemia or extramedullary infiltration
  • Uncontrolled diabetes with glycated hemoglobin > 7.5%
  • Mental illness preventing treatment or informed consent
  • Other conditions deemed unsuitable by the investigator

AI-Screening

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Trial Site Locations

Total: 1 location

1

Blood Diseases Hospital

Tianjin, Tianjin Municipality, China, 300020

Actively Recruiting

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Research Team

H

Hui Wei, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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