RecruitingPhase 2NCT07304089

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

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of VIM0423 in Individuals With Isolated Dystonia (Stride Dystonia)


Sponsor

Vima Therapeutics

Enrollment

100 participants

Start Date

Feb 5, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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?


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called VIM0423 and a drug called VIM0423 Placebo for people with dystonia. The study is currently recruiting participants at 37 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGVIM0423

VIM0423 is a combination drug product containing two active ingredients (VMA-1001 and VMA-1002)

DRUGVIM0423 Placebo

Matching VIM0423 placebo product containing no active ingredient


Locations(38)

Vima Site #033

Birmingham, Alabama, United States

Vima Site #039

Scottsdale, Arizona, United States

Vima Site #004

Scottsdale, Arizona, United States

Vima Site #028

Sun City, Arizona, United States

Vima Site #042

Irvine, California, United States

Vima Site #030

Los Angeles, California, United States

Vima Site #019

Denver, Colorado, United States

Vima Site #009

Gainesville, Florida, United States

Vima Site #008

Miami, Florida, United States

Vima Site #031

Orlando, Florida, United States

Vima Site #005

Atlanta, Georgia, United States

Vima Site #027

Chicago, Illinois, United States

Vima Site #041

Overland Park, Kansas, United States

Vima Site #043

Baltimore, Maryland, United States

Vima Site #007

Olney, Maryland, United States

Vima Site #032

Boston, Massachusetts, United States

Vima Site #037

East Lansing, Michigan, United States

Vima Site #002

Farmington Hills, Michigan, United States

Vima Site #038

St Louis, Missouri, United States

Vima Site #014

Albuquerque, New Mexico, United States

Vima Site #055

Amherst, New York, United States

Vima Site #018

New York, New York, United States

Vima Site #024

New York, New York, United States

Vima Site #036

Rochester, New York, United States

Vima Site #040

Fayetteville, North Carolina, United States

Vima Site #035

Cincinnati, Ohio, United States

Vima Site #029

Portland, Oregon, United States

Vima Site #020

Philadelphia, Pennsylvania, United States

Vima Site #021

Charleston, South Carolina, United States

Vima Site #016

Memphis, Tennessee, United States

Vima Site #006

Nashville, Tennessee, United States

Vima Site #025

Dallas, Texas, United States

Vima Site #026

Georgetown, Texas, United States

Vima Site #012

Houston, Texas, United States

Vima Site #013

Houston, Texas, United States

Vima Site #011

Richmond, Virginia, United States

Vima Site #023

Kirkland, Washington, United States

Vima Site #015

Spokane, Washington, United States

View Full Details on ClinicalTrials.gov

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NCT07304089


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