A Study to Evaluate the Efficacy, Safety, and Tolerability of VIM0423 in Individuals With Isolated Dystonia
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Dystonia
In brief
Stride Dystonia is a randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety, and tolerability of VIM0423 in individuals with isolated dystonia. The main objectives of this clinical trial are to determine the following: * Does VIM0423 therapy improve dystonia symptoms compared to placebo? * Is VIM0423 well tolerated in individuals with isolated dystonia? and * Do the therapeutic effects of VIM0423 confer improvements on daily function and quality of life?
Key facts
- Study ID
- NCT07304089
- Run by
- Vima Therapeutics
- People needed
- 100
- Starts
- 2026-02-05
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2026-08-04
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participant must be male or nonpregnant female between 18 and 65 years of age (inclusive) at Visit 1 (Screening).
- The participant has a clinical diagnosis of isolated dystonia for at least one year prior to Visit 1 (Screening); has two or more body regions affected by dystonia at Visit 1 (Screening); and has been confirmed by Investigator and Enrollment Authorization Committee.
- The participant may be untreated with BoNT; OR if the participant is being treated with BoNT as part of their standard of care for dystonia, they must meet protocol-specified criteria.
- The participants must meet protocol-specified requirements for baseline scores on the BFM and CGI-S.
Where it is running
- Vima Site #015 — Spokane, Washington, United States (enrolling)
- Vima Site #039 — Scottsdale, Arizona, United States (enrolling)
- Vima Site #004 — Scottsdale, Arizona, United States (enrolling)
- Vima Site #028 — Sun City, Arizona, United States (enrolling)
- Vima Site #042 — Irvine, California, United States (enrolling)
- Vima Site #012 — Houston, Texas, United States (enrolling)
- Vima Site #011 — Richmond, Virginia, United States (enrolling)
- Vima Site #023 — Kirkland, Washington, United States (enrolling)
- Vima Site #033 — Birmingham, Alabama, United States (enrolling)
- Vima Site #019 — Denver, Colorado, United States (enrolling)
- Vima Site #009 — Gainesville, Florida, United States (enrolling)
- Vima Site #008 — Miami, Florida, United States (enrolling)
- Vima Site #031 — Orlando, Florida, United States (enrolling)
- Vima Site #005 — Atlanta, Georgia, United States (enrolling)
- Vima Site #027 — Chicago, Illinois, United States (enrolling)
- Vima Site #041 — Overland Park, Kansas, United States (enrolling)
- Vima Site #043 — Baltimore, Maryland, United States (enrolling)
- Vima Site #007 — Olney, Maryland, United States (enrolling)
- Vima Site #032 — Boston, Massachusetts, United States (enrolling)
- Vima Site #037 — East Lansing, Michigan, United States (enrolling)
- Vima Site #002 — Farmington Hills, Michigan, United States (enrolling)
- Vima Site #038 — St Louis, Missouri, United States (enrolling)
- Vima Site #014 — Albuquerque, New Mexico, United States (enrolling)
- Vima Site #018 — New York, New York, United States (enrolling)
- Vima Site #024 — New York, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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