Actively Recruiting

Age: 0 - 18Years
All Genders
Healthy Volunteers
ID04478006

Driving Therapeutic Progress of Childhood Leukemia Through Advanced Translational Research With Immediate and Long-term Impact. Precision Medicine for Childhood Leukemia.

Led by Chinese University of Hong Kong · Updated on 2026-02-03

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to advance treatment for childhood leukemia, the most common cancer in children. Despite improved outcomes, relapse occurs in 15-40% of cases, often leading to survival rates below 50%. Because increasing standard chemotherapy can cause severe side effects, the study focuses on developing safer, targeted therapies for high-risk patients through two main projects involving genetic analysis and novel antibody development. The first project uses whole-exome and RNA sequencing on children with various types of leukemia to analyze genetic changes and drug sensitivity in samples from blood and bone marrow. The second project develops new antibodies tested in animal models to assess their safety and effectiveness against relapsed or hard-to-treat leukemia. These approaches aim to support precision medicine tailored to each child's leukemia. Participants provide samples for genetic and drug sensitivity testing, which researchers use to identify which patients might benefit from targeted treatments. The study measures include genetic alterations, gene expression, drug sensitivity, and antibody treatment efficacy over up to one year. This research may lead to improved therapies for children with leukemia and has both immediate and long-term goals for treatment progress.

CONDITIONS

Brief Title

Advanced Translational Research on Childhood Leukemia

Who Can Participate

Age: 0 - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), mixed phenotype acute leukemia (MPAL), juvenile myelomonocytic leukemia (JMML), or myelodysplastic syndromes (MDS)
  • Normal bone marrow donor
  • Able to understand English or Chinese
  • Age 18 years or younger
  • Patient or parent/guardian agrees to participate
Not Eligible

You will not qualify if you...

  • Unable to understand English or Chinese
  • Patient or parent/guardian refuses to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Baseline

Participants provide blood and bone marrow samples for genetic analysis and drug sensitivity testing to understand their leukemia profile.

1 to 2 visits depending on sample collection needs

Long-term Monitoring

Duration - Up to 1 year

Participants are monitored through genetic and cytogenetic tests to evaluate disease progression and antibody efficacy over time.

Follow-up visits as scheduled over the year

Trial Site Locations

Total: 1 location

1

Hong Kong Children Hospital

Hong Kong, Hksar, China

Actively Recruiting

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Research Team

K

Kathy Chan, Ph. D.

K

Kam Tong Leung, Ph. D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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