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The primary goal of this study is to validate motor and functional outcomes and refine clinical trial strategies for pediatric-onset FSHD
MOVE Peds is a prospective 2-year study recruiting eighty pediatric participants to accelerate therapeutic development for pediatric-onset FSHD. The study aims to validate outcomes and refine clinical trial strategies. Previous cross-sectional studies suggest that younger age of onset is linked to greater clinical severity and that having 1-3 D4Z4 repeats is associated with extra-muscular complications in pediatric FSHD. Prospective studies in early-onset FSHD have been limited by the small number of sites and low recruitment and follow-up rates. Early-onset pediatric FSHD is of high interest to drug companies because: 1. It results in a more significant disease burden than in adults. 2. Treating FSHD at earlier ages may have a more lasting and profound effect. 3. Genetic, molecular, and clinical factors may differ between pediatric and adult-onset FSHD. 4. Smaller body size and faster progression rates may make AAV-delivered gene therapies more feasible. The FSHD CTRN's previous research showed that the FSHD composite functional measure (FSHD-COM), reachable workspace (RWS), and quantitative MRI measures (qMRI) are responsive to disease progression or treatment in adults with FSHD and correlate with performance. Investigators hypothesize that early changes in qMRI in pediatric subjects will predict 2-year changes in FSHD-COM Peds or RWS.
Age
5 - 17 years
Sex
ALL
Healthy Volunteers
No
Stanford University
Palo Alto, California, United States
University of Iowa
Iowa City, Iowa, United States
University of Kansas Medical Center
Kansas City, Kansas, United States
University of Rochester
Rochester, New York, United States
Duke University
Durham, North Carolina, United States
University of Utah
Salt Lake City, Utah, United States
Murdoch Children's Research Institute
Melbourne, Australia
Start Date
May 22, 2025
Primary Completion Date
May 1, 2027
Completion Date
May 1, 2028
Last Updated
February 25, 2026
80
ESTIMATED participants
Lead Sponsor
University of Kansas Medical Center
Collaborators
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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