Status:
RECRUITING
A Clinical Study of MK-1045 (CN201) in People With Precursor B-cell Acute Lymphoblastic Leukemia (MK-1045-002)
Lead Sponsor:
MSD R&D (China) Co., Ltd.
Conditions:
Acute Lymphoblastic Leukemia
Eligibility:
All Genders
2+ years
Phase:
PHASE1
PHASE2
Brief Summary
Researchers are looking for new ways to treat people with a type of blood cancer called precursor B-cell Acute Lymphoblastic Leukemia (B-ALL) that is relapsed- the cancer has come back after treatment...
Eligibility Criteria
The main inclusion criteria include but are not limited to:
-
Adult participants must be age 18 or older
-
Pediatric participants must be at least 2 years old and less than 18 years old.
-
Diagnosis of precursor B-cell acute lymphoblastic leukemia (B-ALL) and have more than 5% blasts in the bone marrow by morphological assessment
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Participants with Ph-negative B-ALL with any of the following refractory/relapse criteria:
- Failure to achieve complete remission after initial induction therapy;
- Failure to achieve complete remission after salvage treatment;
- Relapse with first remission duration ≤12 months
- Second or later relapse
- Relapse after allogeneic HSCT
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Participants with Ph-positive B-ALL who have received 2 (or more) tyrosine kinase inhibitors (TKIs) and meet the refractory/relapse criteria above or, those with the T315I mutation
The main exclusion criteria include but are not limited to:
- History of Burkitt's leukemia.
- Received anti-CD19 therapy within 3 months prior to entering the study
- Received allogeneic HSCT within 12 weeks prior to entering the study
- Received prior treatment with chimeric antigen receptor T cell (CAR-T) within 3 months prior to entering the study
- History or presence of clinically relevant central nervous system (CNS) pathology
- History of clinically symptomatic metastases to the central nervous system or meninges, or other evidence of uncontrolled metastases to the CNS or meninges
- History of immunodeficiency, including history of any positive test result for human immunodeficiency virus (HIV) antibody.
- History of serious cardiovascular and cerebrovascular disease
- Has active autoimmune diseases that may relapse
Key Trial Info
Start Date :
November 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2028
Estimated Enrollment :
203 Patients enrolled
Trial Details
Trial ID
NCT05579132
Start Date
November 1 2022
End Date
June 30 2028
Last Update
February 13 2026
Active Locations (11)
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1
The Second Affiliated Hospital of Third Military Medical University ( Site 0008)
Chongqing, Chongqing Municipality, China, 400037
2
Southern Medical University Nanfang Hospital ( Site 0004)
Guangzhou, Guangdong, China, 510515
3
The Second Hospital of Hebei Medical University ( Site 0003)
Shijiazhuang, Hebei, China, 050000
4
The First Hospital of Harbin ( Site 0005)
Harbin, Heilongjiang, China, 150010