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

  • 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
  • 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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Page 1 of 3 (11 locations)

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

A Clinical Study of MK-1045 (CN201) in People With Precursor B-cell Acute Lymphoblastic Leukemia (MK-1045-002) | DecenTrialz