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NCT06390306Recruiting

The Efficacy and Safety of Third-generation TKIs Combined With Azacitidine and Bcl-2 Inhibitor in Patients With CML-MBP

The Efficacy and Safety of Third Generation Tyrosine Kinase Inhibitors Combined With Azacitidine and B-cell Lymphoma-2 Inhibitor in Patients With Myeloid Blast Phase Chronic Myeloid Leukemia

Source: ClinicalTrials.gov · Last updated 3 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a prospective multi-center study to investigate efficacy and safety of the third generation tyrosine kinase inhibitors (TKIs) combined with azacitidine and B-cell lymphoma-2 (Bcl-2) inhibitor in patients with myeloid blast phase chronic myeloid leukemia (CML-MBP).

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
18 Apr 2024
Start date
1 Jul 2024
Primary completion date
1 Dec 2026
Lead sponsor
Peking University People's Hospital
NCT number
NCT06390306

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 1 Jul 2024 to the primary completion date, 1 Dec 2026
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • concurrent diseases requiring treatment(s) with potential to interact with 3G-TKI;

Other illness

  • diagnosis of other primary malignancies;
  • history of allogeneic HSCT;
  • extramedullary disease only.

Who the study is looking for

  • age ≥ 18 years old;
  • philadelphia chromosome (Ph)-positive or BCR::ABL-positive;
  • serum creatinine ≤ 1.5 × upper limit of normal (ULN) or 24h creatinine clearance ≥ 50 mL/min when serum creatinine was \> 1.5 × ULN;
  • serum total bilirubin ≤ 1.5 × ULN;
  • aspartate aminotransferase and alanine aminotransferase ≤ 2.5 × ULN;
  • amylase ≤ 1.5 × ULN; (7) lipase ≤ 1.5 × ULN;
  • ejection fraction \> 50%; corrected QT interval on electrocardiographic evaluation was ≤ 450 ms in men or ≤ 470 ms in women.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chuiyangliu hospital affiliated to tsinghua university
Coordinator of this site? Confirm its status
BeijingChinaNot yet recruiting
Peking University People's Hospital
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BeijingChinaRecruiting
Beijing Lu Daopei Hospital
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BeijingChinaRecruiting
Sichuan Provincial People's Hospital
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ChengduChinaNot yet recruiting
Nanfang Hospital, Southern Medical University
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GuangdongChinaNot yet recruiting
The First Affiliated Hospital of Kunming Medical University
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KunmingChinaNot yet recruiting
The First Affiliated Hospital of Nanjing Medical University
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NanjingChinaRecruiting
The First Affiliated Hospital of Guangxi Medical University
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NanningChinaRecruiting
Nanyang Central Hospital
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NanyangChinaRecruiting
Ningbo Medical Center Lihuili Hospital
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NingboChinaRecruiting
Qilu Hospital of Shandong University
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QiluChinaNot yet recruiting
Chinese Academy of Medical Sciences & Peking Union Medical College Hospital
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TianjinChinaNot yet recruiting
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Henan Cancer Hospital
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WuhanChinaNot yet recruiting
Xi'an International Medical Center Hospital
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Xi'anChinaRecruiting
The First Affiliated Hospital, Zhejiang University School of Medicine
Coordinator of this site? Confirm its status
ZhejiangChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.