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A Long-Term Follow-up Study to Evaluate the Safety and Efficacy of Adeno Associated Virus (AAV) Serotype 8 (AAV8)-Mediated Gene Transfer of Glucose-6-Phosphatase (G6Pase) in Adults With Glycogen Storage Disease Type Ia (GSDIa)
The primary objective of this study is to determine the long-term safety of DTX401 following a single intravenous (IV) dose in adults with GSDIa.
Only participants who received DTX401 in study 401GSDIA01 (NCT03517085) are eligible to participate in study 401GSDIA02. No investigational product will be administered during study 401GSDIA02. Participants will be followed in study 401GSDIA02 for at least 4 years, and up to 6 years after administration of DTX401.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
UCONN Health
Farmington, Connecticut, United States
Michigan Medicine University of Michigan
Ann Arbor, Michigan, United States
University of Texas Health Science Center at Houston
Houston, Texas, United States
Montreal Children Hospital, McGill University Health Centre
Montreal, Quebec, Canada
University Medical Center Groningen
Groningen, Netherlands
Complejo Hospitalario Universitario de Santiago
Santiago de Compostela, A Coruna, Spain
Start Date
July 15, 2019
Primary Completion Date
February 25, 2025
Completion Date
February 25, 2025
Last Updated
March 18, 2026
12
ACTUAL participants
No intervention
OTHER
Lead Sponsor
Ultragenyx Pharmaceutical Inc
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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