A Prospective and Retrospective Data Collection Study to Evaluate Outcomes in Males ≤17 Years of Age Undergoing Allogeneic Hematopoietic Stem Cell Transplantation for the Treatment of Cerebral Adrenoleukodystrophy

Status: Terminated
Location: See all (13) locations...
Intervention Type: Genetic
Study Type: Observational
SUMMARY

Study ALD-103 will be a multi-site, global, prospective and retrospective data collection study that is designed to evaluate outcomes of allo-HSCT in male subjects with CALD ≤17 years of age.

Eligibility
Participation Requirements
Sex: Male
Maximum Age: 17
Healthy Volunteers: f
View:

• Provide informed consent from a competent custodial parent or guardian with legal capacity to execute a local Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved consent. In addition, informed assent will be sought from capable subjects, in accordance with the directive of the institution's IRB/IEC and all other local requirements.

• Be male and ≤17 years of age at the time of treatment, for retrospective and partial prospective/retrospective subjects, or at the time of parental/guardian consent and, where appropriate, subject assent, for prospective subjects.

• Have a confirmed diagnosis of CALD as defined by abnormal VLCFA profile and cerebral lesion on brain MRI.

• Depending on the cohort, the subject must:

‣ Be scheduled for allo-HSCT evaluation at a study site (prospective cohort only),

⁃ Have received an allo-HSC infusion and be consented in time to complete the Month 24 Visit on study (partial prospective/retrospective cohort only), or

⁃ Have received their most recent allo-HSC infusion on or after January 1, 2013 (retrospective cohort only).

Locations
United States
California
Children's Hospital Los Angeles
Los Angeles
Stanford University
Palo Alto
Massachusetts
Boston Children's Hospital/Massachusetts General Hospital
Boston
Minnesota
University of Minnesota
Minneapolis
North Carolina
Duke University Medical Center
Durham
Pennsylvania
The Children's Hospital of Philadelphia
Philadelphia
Other Locations
Argentina
Hospital Austral
Buenos Aires
Canada
McGill University Health Centre
Montréal
Germany
University Hospital Leipzig
Leipzig
Italy
IRCCS Ospedale Pediatrico Bambine Gesú
Roma
Netherlands
Princess Maxima Center for Pediatric Oncology (PMC)
Utrecht
United Kingdom
Great Ormond Street Hospital
London
Central Manchester University Hospitals NHS Foundation Trust
Manchester
Time Frame
Start Date: 2015-04
Completion Date: 2019-12-06
Participants
Target number of participants: 59
Treatments
Allo-HSCT prospective
Subjects who will be consented before they received an allo-HSC infusion. They will be consented and enrolled on the study during the Screening Period.
Allo-HSCT partial prospective/retrospective
Subjects who will be consented after they received an allo-HSC infusion but before they reach 24 months post-infusion on study. Subjects in this cohort will participate prospectively in at least the Month 24 Visit in order to obtain prospective on-study data for this and all visits after Month 24
Allo-HSCT retrospective
Subjects who received an allo-HSC infusion on or after January 1, 2013 and died before study data collection.
Sponsors
Leads: bluebird bio

This content was sourced from clinicaltrials.gov