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Study identifier: NCT07700225 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Establishing Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1) Extension

Condition: DM1 · Myotonic Dystrophy · Myotonic Dystrophy 1  ·  Sponsor: Virginia Commonwealth University

PhaseN/A
Planned participants1000
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

Myotonic Dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder that causes progressive disability and shortened life expectancy. It is characterized by progressive weakness and myotonia, which preferentially affects the craniofacial, hand, and distal leg muscles. Many patients also experience difficulties with cognition, cardiac arrhythmias, respiratory failure, or cataracts. Currently there is no treatment to slow progression or reverse the symptoms.

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

Talk to the study team

Jennifer Raymond  ·  804-828-6318  ·  Jennifer.raymond@vcuhealth.org

Ruby Langeslay  ·  804-828-6318  ·  Ruby.langeslay@vcuhealth.org

Always discuss trial participation with your own doctor first.

Locations (1)

Virginia Commonwealth UniversityRichmond, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07700225