Summary
This is a multi-center, long-term safety and efficacy follow-up study for participants with cerebral adrenoleukodystrophy (CALD) who have received Lenti-D Drug Product (eli-cel) in a parent clinical study. After completing a parent clinical study (approximately 2 years), eligible participants will be followed for an additional 13 years for a total of 15 years post-drug product infusion. No investigational drug product will be administered in this study.
Conditions
Cerebral Adrenoleukodystrophy (CALD), Adrenoleukodystrophy (ALD), X-Linked Adrenoleukodystrophy (X-ALD)
Recruitment Status
Active, not recruiting
Eligibility Criteria
Inclusion Criteria:
Provision of written informed consent for this study by the participant or participant's parent(s)/ legal guardian(s) and written informed assent by participant, if applicable
Have received eli-cel in a parent clinical study
Exclusion Criteria:
There are no exclusion criteria for this study
Intervention
Intervention Type
Intervention Name
Genetic
Lenti-D Drug Product
Gender
Male
Min Age
N/A
Max Age
N/A
Download Date
February 7, 2024
Principal Investigator
N/A
Primary Contact Information
For more information on this trial, visit clinicaltrials.gov.
Contact
For more information and to contact the study team: