Estab Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1)
Key facts
- Who runs it
- Virginia Commonwealth University
- Where
- Columbus, Denver, Gainesville, Houston, Iowa City, Kansas City, La Jolla, Los Angeles, Richmond, and Rochester, United StatesSee the 10 sitesAlso in 6 other countries, 7 sites
- Trial code
- Status
- Recruiting
- People taking part
- 700 people, planned
- Started
- 1 Jan 2019
- Expected to end
- 1 Dec 2026
- Type of study
- Observational
- Record updated
- 3 November 2026
Who can take part
- Age
- 18 years to 70 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 18 criteriaShow less
Who can take part
- Age 18 to 70 (inclusive)
- Competent to provide informed consent
- Clinical diagnosis of DM1 based on research criteria1 or positive genetic test
- Comment: The clinical research criteria require myotonia, muscle weakness in a characteristic distribution, and history of similar findings in a first degree relative. Genetic testing confirmed the diagnosis of DM1 in > 99% of individuals who satisfied these criteria.2
- Of the 95 patients undergoing the tibialis anterior muscle biopsy, at least half will have at least moderate weakness of ankle dorsiflexion, defined as MRC score ≤ 4+. This is in order to obtain a muscle tissue sample in a person more severely affected with myotonic dystrophy. Approximately 10 patients at each site will undergo the muscle biopsy
Who cannot take part
- Concurrent enrollment in clinical trial for DM1, or participation in trial within 6 months of entry
- Concurrent pregnancy or planned pregnancy during the course of the study
- Concurrent medical condition that would, in the opinion of the investigator or clinical evaluator, compromise performance on study measures
- Use of aspirin or non-steroidal anti-inflammatory agents should be discontinued 3 days prior to the biopsy procedure, if possible
- Previous muscle biopsy of either TA in order to provide muscle tissue samples of non-biopsied muscles
- Symptomatic renal or liver disease, uncontrolled diabetes or thyroid disorder, or active malignancy other than skin cancer
- Use of anticoagulant such as warfarin or a direct oral anticoagulant (e.g. dabigatran) due to the increased risk of bleeding
- History of a bleeding disorder due to the increased risk of bleeding
- Platelet count <50,000 (if known) due to the increased risk of bleeding
- Current alcohol or substance abuse
- Note: non-ambulatory participants are not excluded, but are limited to <15% of enrollment
- Known CTG repeat expansion size less than 100 repeats, unless there are clear cut signs of limb weakness and muscle wasting. This is in order to obtain a muscle tissue sample in a person more severely affected with myotonic dystrophy
- Advanced wasting of tibialis anterior (TA) muscle that precludes needle muscle biopsy in order to ensure that a sample taken would be of muscle and not just fat and fascia
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 70 years old?
Where in United States
Also in 6 other countries, 7 sites
- Ohio State UniversityColumbus, United StatesContact: Kaneshia HivesTaking people
- University of Colorado DenverDenver, United StatesContact: Alyssa AvilezTaking people
- University of FloridaGainesville, United StatesContact: Whitney MillerTaking people
- Houston Methodist Neurological InstituteHouston, United StatesContact: Kadeesia BrownTaking people
- University of IowaIowa City, United StatesContact: Maegan TyrrellTaking people
- Kansas University Medical CenterKansas City, United StatesContact: Rebecca ClayTaking people
- University of California San DiegoLa Jolla, United StatesContact: Elizabeth MorenoTaking people
- University of California, Los AngelesLos Angeles, United StatesContact: Dennis FernandoTaking people
- Virginia Commonwealth UniversityRichmond, United StatesContact: Carino JenningsTaking people
- University of RochesterRochester, United StatesContact: Jim HilbertTaking people
About the trial
What the trial wants to find out
Building on previous work of the Myotonic Dystrophy Clinical Research Network (DMCRN), the present study seeks to overcome insufficient data on natural history; lack of reliable biomarkers; and incomplete characterization and limited biological understanding of the phenotypic heterogeneity of Myotonic Dystrophy 1 by examining strategies to improve the reliability by making further refinements in our sample collection and analysis procedures by developing strategies for managing patient heterogeneity going forward.
Read full original descriptionShow less
Funding Source- FDA OOPD
The group in the trial
- Study Visits
Patients will receive standard of care as determined by their treating physician. Study visits occur at baseline/0 months, 12 months, and 24 months
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Establishing Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1)
- Fit questions
- Built from NCT03981575, who can take part
- Publications
- Record updated
- 3 November 2026