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Studies biology and symptoms of ALS to aid new drug research

Collects data from adults with ALS and healthy volunteers to study the disease.

Plain-language title generated from the registry record
Registry title: ALS Research Collaborative

Key facts

Where
Watertown, United StatesSee the site

Where in United States

  • ALS Therapy Development InstituteWatertown, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
ALS Therapy Development Institute
Trial code
NCT06885918
Record updated
20 March 2025
Original description
The goal of this natural history study is to learn more about the biological and clinical aspects of amyotrophic lateral sclerosis (ALS). This study's findings will help with drug discovery, biomarker discovery, and outcome measure validation. Adults living with ALS, other motor neuron diseases (MND), a known mutation related to ALS and healthy volunteers contribute prospective and retrospective data to this study remotely. The study is sponsored and conducted by the ALS Therapy Development Institute.Read full original descriptionShow less

ALS Translational Research Program

The goal of this natural history study is to learn more about the biological and clinical aspects of amyotrophic lateral sclerosis (ALS). This study's findings will help with drug discovery, biomarker discovery, and outcome measure validation. Adults living with ALS, other motor neuron diseases (MND), a known mutation related to ALS and healthy volunteers contribute prospective and retrospective data to this study remotely. The study is sponsored and conducted by the ALS Therapy Development Institute.

Inclusion: 18 years of age or older; Can communicate in written English; Has a diagnosis of ALS/MND or is a known carrier of an ALS associated mutation.

Exclusion: Significant cognitive impairment that would prevent individual completion and understanding of the informed consent process.

ClinicalTrials.gov NCT06885918