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Study to Evaluate Biomarkers and Clinical Manifestations in Individuals With Glycogen Storage Disease Type III (GSD III)

Completed
Conditions
Glycogen Storage Disease Type III
Registration Number
NCT04574830
Lead Sponsor
Ultragenyx Pharmaceutical Inc
Brief Summary

The primary objective of this study is to evaluate potential biomarkers of GSD III.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
18
Inclusion Criteria
  • Confirmed historical diagnosis of GSD III based on pathogenic mutations in the AGL gene on both alleles or GDE deficiency based on biopsy of liver, muscle, or fibroblasts
  • Willing to comply with all study procedures
  • Willing and able to provide written informed consent. If a minor, willing and able to provide written assent and have a legally authorized representative willing and able to provide written informed consent
Exclusion Criteria
  • Presence or history of any condition that, in the view of the Investigator, places the subject at high risk of poor study compliance, interferes with study participation, or interferes with the subject's ability to safely or reliably complete the study assessments
  • Use of any IP within 30 days prior to informed consent/assent or at the time of enrollment

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Urine hexose tetrasaccharide (Hex4): mean and varianceUp to Day 35
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

Children's Hospital Orange County

🇺🇸

Orange, California, United States

Colorado Children's Hospital

🇺🇸

Aurora, Colorado, United States

University of Texas Medical School

🇺🇸

Houston, Texas, United States

University of California

🇺🇸

Irvine, California, United States

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