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RecruitingPhase 2

A Study to Evaluate the Efficacy, Safety, and Tolerability of VIM0423 in Individuals With Isolated Dystonia

Vima Therapeutics · NCT07304089

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–70 · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 2
Target enrollment
100
US sites recruiting
37
Study start
February 5, 2026
Record last updated
October 22, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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?

Being studied: VIM0423; VIM0423 Placebo

Conditions: Dystonia

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Participant must be male or nonpregnant female between 18 and 70 years of age (inclusive) at Visit 1 (Screening).
  • The participant has a clinical diagnosis of isolated dystonia with symptoms consistent with 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.

Recruiting US locations

  • Vima Site #033

    Birmingham, AL 35233

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #039

    Scottsdale, AZ 85251

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #004

    Scottsdale, AZ 85258

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #028

    Sun City, AZ 85351

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #042

    Irvine, CA 92614

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #030

    Los Angeles, CA 90048

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #019

    Denver, CO 80113

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #009

    Gainesville, FL 32608

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #008

    Miami, FL 33176

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #031

    Orlando, FL 32825

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #005

    Atlanta, GA 30329

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #027

    Chicago, IL 60611

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #041

    Overland Park, KS 66211

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #043

    Baltimore, MD 21237

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #007

    Olney, MD 20832

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #032

    Boston, MA 02215

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #037

    East Lansing, MI 48824

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #002

    Farmington Hills, MI 48334

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #038

    St Louis, MO 63110

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #014

    Albuquerque, NM 87106

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #018

    New York, NY 10019

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #024

    New York, NY 10021

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #036

    Rochester, NY 14618

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #040

    Fayetteville, NC 28304

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #035

    Cincinnati, OH 45212

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #029

    Portland, OR 97239

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #020

    Philadelphia, PA 19107

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #021

    Charleston, SC 29425

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #016

    Memphis, TN 38157

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #006

    Nashville, TN 37232

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #025

    Dallas, TX 75390

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #026

    Georgetown, TX 78628

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #012

    Houston, TX 77030

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #013

    Houston, TX 77030

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #011

    Richmond, VA 23233

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #023

    Kirkland, WA 98034

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

  • Vima Site #015

    Spokane, WA 99202

    Site contact: Study Director · 617-430-7027 · clinicaltrials@vimatx.com

Study contacts (from the official record)

  • Study Director · 617-430-7027 · Clinicaltrials@vimatx.com
A Study to Evaluate the Efficacy, Safety, and Tolerability of… (NCT07304089) | Bored Studies