Clin2
NCT07703462Worth exploringEnrolling by invitation

Personalized therapy for TARDBP ALS

Amyotrophic Lateral Sclerosis (ALS)

Part of Brain & nervous system, Hormones & metabolism clinical trials.

This trial offers a custom-made treatment for people with ALS caused by a TARDBP gene mutation. It uses a personalized medicine approach to target the specific genetic cause of the disease.

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

Phase
Phase 1/Phase 2
Enrollment
1 people
Ages
Any age
Study type
Interventional

Who can take part

  • You must have a genetically confirmed neurological disorder, specifically ALS linked to TARDBP.
  • You or your legal representative must agree to participate and sign a consent form.
  • You must be able to travel to the study site for all follow-up visits and tests.
  • You must not be using any other experimental medication within 5 half-lives before starting the trial.

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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