STRIDE DYSTONIA VIM0423-201

Recruiting
18 years - 65 years
All
Phase 2
1 Location

Brief description of study

To evaluate the clinical efficacy of VIM0423 compared to placebo in individuals with isolated dystonia.

Detailed description of study

The study medication is a new medication that has been evaluated in Phase 1 studies in both healthy adults and in adults with isolated dystonia. The study medication is taken daily as a combination of oral tablets from 2 separate bottles. It is designed to target receptors in the brain that are involved in dystonia and related movement disorders. Currently, there is no treatment option for all types of dystonia and no oral drugs approved. Study medications available through clinical research studies make it possible for doctors to discover potential treatments for rare diseases, like isolated dystonia

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Dystonia
  • Age: 18 years - 65 years
  • Gender: All

  • Male or nonpregnant female 18-65 years of age
  • Diagnosis of isolated dystonia for at least 1 year
  • Have not been treated with botulinum toxins (BoNT) OR are being treated with BoNT as standard of care for dystonia (other criteria apply if you are being treated with BoNT)

Updated on 07 Apr 2026. Study ID: 25-2055

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