Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:53 PM
Ignite Modification Date:
2025-12-24 @ 11:53 PM
NCT ID:
NCT05967351
Eligibility Criteria:
Inclusion Criteria:
* Received delandistrogene moxeparvovec for Duchenne muscular dystrophy in a previous clinical study.
* Has (a) parent(s) or legal caregiver(s) or is ≥18 years of age and able to understand and comply with the study visit schedule and all other protocol requirements.
Exclusion Criteria:
* Participant or family does not want to disclose participation with general practitioner/primary care physician and other medical providers.
Other inclusion/exclusion criteria may apply.
Healthy Volunteers:
False
Sex:
MALE
Study:
NCT05967351
Study Brief:
Protocol Section:
NCT05967351