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Clinical Trials in Denmark / NCT05270096
Recruiting Observational

International Leukemia Target Board

NCT05270096 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2022-12-31
Last updated
2026-01-09

Condition(s) studied

Relapsed Hematologic MalignancyRefractory Hematologic Malignancy

Investigational drug(s) / intervention(s)

Advice

Advice: non-interventional study

Study summary

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.

Eligibility

Sex
ALL
Min age
0 Years
Max age
25 Years
Healthy volunteers
No
Inclusion criteria 1. The patient has been diagnosed with a R/R hematological malignancy; 2. The patient is less than 18 years of age at the time of first diagnosis and less than 25 years at the time of inclusion with relapse/refractory hematological malignancy; 3. The patient is treated in a pediatric/AYA setting or study protocol, with no current standard of care treatment; 4. The patients' life expectancy is at least 6 weeks; 5. The patient has undergone any sort of molecular profiling of his/her tumor and the re-sults of this analysis are available; 6. The patient has undergone flow cytometry in a certified lab and results are available; 7. Written informed consent of patient and/or parent(s)/guardian(s) to discuss the patient in the iLTB according to local law and legislation has been obtained. Exclusion criteria: none defined

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
UH Gent Ghent Belgium Recruiting
Righospitalet Copenhagen Denmark Recruiting
Semmelweis Budapest Hungary Recruiting
Princess Máxima Center for Pediatric Oncology Utrecht Utrecht Recruiting
Vall d'Hebron Barcelona Spain Recruiting
Queen Silvia Gothenburg Sweden Recruiting
Newcastle Hospital Newcastle United Kingdom Recruiting

More Princess Maxima Center for Pediatric Oncology trials in Denmark

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05270096 on ClinicalTrials.gov ↗ ← All trials in Denmark