Clinical Trial

International Leukemia Target Board

Study acronym: iLTB
Recruiting
View on ClinicalTrials.gov →
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.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2022-02-25; most recent amendment 2026-01-07.
Status change: Not Yet Recruiting → Recruiting 2023-02-09
Trial Details
NCT Number NCT05270096
Lead Sponsor Princess Maxima Center for Pediatric Oncology
Conditions Relapsed Hematologic Malignancy, Refractory Hematologic Malignancy
Enrollment 600 participants
Start Date 2022-12-31
Primary Completion 2030-07-01 (estimated)
Study Completion 2032-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-01-09