Actively Recruiting

Age: 0Years - 25Years
All Genders
ID05270096

International Concerted Action to Allocate Children, Adolescents and Young Adults With Relapsed and Refractory Leukemia/Lymphoma to the Right Therapy

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

600

Participants Needed

7

Research Sites

100 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a new approach called the international Leukemia Target Board (iLTB) for children, adolescents, and young adults with relapsed or refractory blood cancers. The iLTB aims to bring together experts across Europe to review molecular, immunophenotypic, and drug response data from each patient to prioritize potential treatment options. This non-interventional study seeks to provide uniform advice to treating physicians and facilitate access to early phase clinical trials or alternative treatments when standard options are limited. The iLTB does not provide treatments directly but serves as a platform where experts discuss patients' genetic lesions, surface antigen markers, and drug response profiles. Patients eligible for discussion have relapsed or refractory hematological malignancies and have undergone molecular profiling and flow cytometry. The expert panel uses a prioritization algorithm to recommend potential therapies or trial options, considering each patient's treatment history and goals. Patient data is shared following informed consent and feedback is given to the treating physician. Participants are involved through data sharing and expert review of their tumor profiles, but no treatment is administered by the study itself. The study tracks how often physicians follow the iLTB advice, what therapies are chosen, and patient outcomes over time. The main measure is the proportion of patients receiving therapy aligned with iLTB recommendations, monitored over about 8 years. This long-term registry helps assess the impact of expert advice on treatment decisions and outcomes for this challenging patient group.

CONDITIONS

Brief Title

International Leukemia Target Board

Who Can Participate

Age: 0Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient has been diagnosed with a relapsed or refractory hematological malignancy
  • Patient is less than 18 years old at first diagnosis and less than 25 years old at time of inclusion
  • Patient is treated in a pediatric or adolescent/young adult setting with no current standard of care treatment
  • Patient's life expectancy is at least 6 weeks
  • Patient has molecular profiling results of their tumor available
  • Patient has flow cytometry results from a certified lab available
  • Written informed consent to discuss the patient in the international Leukemia Target Board has been obtained according to local laws
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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 8 years

Participants who undergo routine care are observed through an international platform where experts review molecular profiling and other diagnostic information to advise on the most appropriate treatment options.

Data sharing and discussion occur as needed; no additional study visits required

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

Loading map...

Research Team

U

Uri Ilan, MD

A

Anne Elsinghorst

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

Similar Trials

A Phase Ia/Ib Open-label Dose Escalation and Expansion Study...

Advanced Solid Tumors

Actively Recruiting

8 locations

Open-Label Dose Escalation and Expansion Trial of Emavuserti...

Relapsed Hematologic Malignancy

Actively Recruiting

45 locations

Long-term Follow-up After Adoptive Transfer of Genetically M...

Relapsed Hematologic Malignancy

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here