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Study identifier: NCT07038200 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD

Condition: Facioscapulohumeral Muscular Dystrophy · FSHD · FSHD - Facioscapulohumeral Muscular Dystrophy  ·  Sponsor: Avidity Biosciences, Inc.

PhasePhase 3
Planned participants200
Who can joinAll sexes, 16 Years to 70 Years
Healthy volunteersNo

About this study

A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Intravenous AOC 1020 for the Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD)

This description comes directly from the study's public registry record.

Talk to the study team

Avidity Biosciences, Inc., A Novartis Company  ·  1-888-669-6682  ·  novartis.email@novartis.com

Avidity Biosciences, Inc., A Novartis Company  ·  +41613241111  ·  novartis.email@novartis.com

Always discuss trial participation with your own doctor first.

Locations (46)

University of California IrvineOrange, California, United StatesActive Not Recruiting
Stanford UniversityPalo Alto, California, United StatesActive Not Recruiting
University of ColoradoDenver, Colorado, United StatesActive Not Recruiting
University of FloridaGainesville, Florida, United StatesActive Not Recruiting
University of IowaIowa City, Iowa, United StatesActive Not Recruiting
Kansas University Medical CenterKansas City, Kansas, United StatesActive Not Recruiting
Kennedy Krieger InstituteBaltimore, Maryland, United StatesActive Not Recruiting
University of MassachusettsWorcester, Massachusetts, United StatesActive Not Recruiting
University of Rochester Medical CenterRochester, New York, United StatesActive Not Recruiting
Duke UniversityDurham, North Carolina, United StatesActive Not Recruiting
Ohio State UniversityColumbus, Ohio, United StatesActive Not Recruiting
University of PennsylvaniaPhiladelphia, Pennsylvania, United StatesActive Not Recruiting

+ 34 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07038200