Clin2
NCT07609108Likely a fitRecruiting

Pridopidine to slow Huntington's disease progression

Huntington Disease

Treatments studied

Part of Brain & nervous system, Genetic & congenital, Mental health clinical trials.

This study tests whether a medication called pridopidine can help slow the progression of Huntington's disease symptoms in adults. Huntington's is a genetic disorder affecting movement, mood, and thinking, and this trial aims to see if pridopidine improves daily functioning and quality of life.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
400 people
Ages
23 years to 65 years
Study type
Interventional

Who can take part

  • You have a confirmed Huntington's disease diagnosis with the genetic mutation (≥40 CAG repeats) and clear motor symptoms
  • You are at least 21 years old and had symptom onset at age 21 or later
  • You still have significant functional ability (score of 7 or higher on a standard scale)
  • You have moderate motor symptoms (a score of 20 or higher on movement testing)
  • You have not taken certain movement-disorder medications (VMAT2 inhibitors or antipsychotics) for at least 6 months
  • You don't have serious heart conditions, recent seizures, or other major medical or psychiatric problems that could interfere with the study

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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