Study of the Oral Treatment MTR-601 in Cervical Dystonia
Paused · Phase 2 · Has a placebo group
Conditions studied: Cervical Dystonia
In brief
Study MTR-601-201 is an 8-week, randomized, placebo-controlled study to examine the safety, tolerability, and efficacy of MTR-601 in participants with cervical dystonia.
Key facts
- Study ID
- NCT06830642
- Run by
- Motric Bio
- People needed
- 80
- Starts
- 2025-02-28
- Expected to finish
- 2026-08-03
- Last updated by the study team
- 2025-12-12
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Arizona Neuroscience Research, LLC — Phoenix, Arizona, United States
- The Parkinson's and Movement Disorder Institute — Fountain Valley, California, United States
- Keck Medicine of University of Southern California — Los Angeles, California, United States
- CenExel Rocky Mountain Clinical Research — Englewood, Colorado, United States
- Neurology One — Orlando, Florida, United States
- University of South Florida — Tampa, Florida, United States
- Emory University — Atlanta, Georgia, United States
- Rush University Medical Center — Chicago, Illinois, United States
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Michigan State University, Department of Neurology — East Lansing, Michigan, United States
- Quest Research Institute — Farmington Hills, Michigan, United States
- University of New Mexico, The Nene and Jamie Koch Comprehensive Movement Disorder Clinic — Albuquerque, New Mexico, United States
- Albany Medical Center Neurosciences Institute — Albany, New York, United States
- Icahn School of Medicine at Mount Sinai — New York, New York, United States
- Vanderbilt Neurology, The Vanderbilt Clinic — Nashville, Tennessee, United States
- Kingfisher Cooperative, LLC — Spokane, Washington, United States
- West Virginia University Medicine — Morgantown, West Virginia, United States
Full record on ClinicalTrials.gov
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