Actively Recruiting

Age: 0Years - 25Years
All Genders
NCT05270096

International Leukemia Target Board

Led by Princess Maxima Center for Pediatric Oncology · Updated on 2026-01-09

600

Participants Needed

7

Research Sites

491 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The iLTB is a proof-of-concept initiative for children with r/r hematological malignancies, in which available treatment options will be prioritized by actionable events in a harmonized and uniform setting across Europe by a team of biologists, bio-statisticians, bio-informaticians, disease experts, geneticists, flow-experts, clinical trial physicians and also the treating physician. The iLTB will discuss molecular (genetic lesions), immunophenotypic/surface antigen markers information and, if available, drug response profiles to prioritize these events taking into account the treatment history and treatment intention (bridging to hematopoietic stem cell transplanation/CAR-T or palliative) of each patient followed by a registry to monitor how often iLTB advice has been followed, which other therapy was chosen (off-label, compassionate use) and what the patient outcome is at an aggregated level. As such the iLTB is non-interventional as it mainly provides advice and registers data on patients discussed in the iLTB.

CONDITIONS

Official Title

International Leukemia Target Board

Who Can Participate

Age: 0Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • The patient has been diagnosed with a relapsed or refractory hematological malignancy
  • The patient is less than 18 years old at first diagnosis and less than 25 years old at inclusion with relapsed/refractory disease
  • The patient is treated in a pediatric or adolescent/young adult setting or study protocol with no current standard treatment
  • The patient has a life expectancy of at least 6 weeks
  • The patient has undergone molecular profiling of their tumor and results are available
  • The patient has undergone flow cytometry in a certified lab and results are available
  • Written informed consent from patient and/or parent(s)/guardian(s) to discuss the patient in the iLTB has been obtained
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 7 locations

1

UH Gent

Ghent, Belgium

Actively Recruiting

2

Righospitalet

Copenhagen, Denmark

Actively Recruiting

3

Semmelweis

Budapest, Hungary

Actively Recruiting

4

Princess Máxima Center for Pediatric Oncology

Utrecht, Utrecht, Netherlands, 3584CS

Actively Recruiting

5

Vall d'Hebron

Barcelona, Spain

Actively Recruiting

6

Queen Silvia

Gothenburg, Sweden

Actively Recruiting

7

Newcastle Hospital

Newcastle, United Kingdom

Actively Recruiting

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Research Team

U

Uri Ilan, MD

CONTACT

A

Anne Elsinghorst

CONTACT

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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