A Gene Transfer Therapy Study to Evaluate the Safety of and Expression From Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD)
Trial ID or NCT#
NCT04626674
Status
RECRUITING
Purpose
This is an open-label gene transfer therapy study evaluating the safety of and expression from delandistrogene moxeparvovec in participants with DMD. The maximum participant duration for this study is 156 weeks.
Official Title
An Open-Label, Systemic Gene Delivery Study Using Commercial Process Material to Evaluate the Safety of and Expression From SRP-9001 in Subjects With Duchenne Muscular Dystrophy (ENDEAVOR)
Eligibility Criteria
Ages Eligible for Study: Older than 2 Years
Sexes Eligible for Study: Male
Accepts Healthy Volunteers: No
Inclusion Criteria:
- - For Cohorts 1-7: Has a definitive diagnosis of DMD based on documented clinical findings and prior genetic testing. - Cohort 1: Is ambulatory, and ≥4 to <8 years of age at the time of Screening. - Cohort 2: Is ambulatory, and ≥8 to <18 years of age at the time of Screening. - Cohort 3: Non-ambulatory per protocol specified criteria at the time of Screening. - Cohort 4: Is ambulatory and ≥3 to <4 years of age at the time of Screening. - Cohort 5a: Is ambulatory and ≥4 to <9 years of age. - Cohort 5b: Non-ambulatory per protocol specified criteria at the time of Screening. - Cohort 6: Is ambulatory, and ≥2 to <3 years of age at the time of Screening. - Cohort 7: Non-ambulatory per protocol-specified criteria at the time of Screening. - Ability to cooperate with motor assessment testing. - Cohorts 1, 2, 3, 5, and 7 only: Stable dose equivalent of oral glucocorticoids for at least 12 weeks before screening and the dose is expected to remain constant (except for modifications to accommodate changes in weight) throughout the first year of the study. - Cohorts 4 and 6: Do not yet require use of chronic steroids for treatment of their DMD, in the opinion of the Investigator, and are not receiving steroids at the time of Screening. - rAAVrh74 antibody titers are not elevated as per protocol-specified requirements. - Genetic mutation inclusion criteria vary by cohort.
Exclusion Criteria:
- - Has a concomitant illness, autoimmune disease, chronic drug treatment, and/or cognitive delay/impairment that in the opinion of the Investigator creates unnecessary risks for gene transfer. - Exposure to gene therapy, investigational medication, or any treatment designed to increase dystrophin expression within protocol-specified time limits. - Abnormality in protocol-specified diagnostic evaluations or laboratory tests. Other inclusion/exclusion criteria apply.
Investigator(s)
John W. Day, MD, PhD
Neuromuscular neurologist,
Neurophysiologist
Professor of Neurology (Adult Neurology), of Pediatrics (Genetics) and, by courtesy, of Pathology
Contact us to find out if this trial is right for you.
Contact
SPECTRUM
650-725-4341
View on ClinicalTrials.gov
