Phase 1Recruiting

Acamprosate in C9orf72 Hexanucleotide Repeat Expansion Amyotrophic Lateral Sclerosis (ACALS)

Sponsor
National Institute of Neurological Disorders and Stroke (NINDS) (NIH)
Enrolment
30 planned
Conditions
Amyotrophic Lateral Sclerosis; Motor Neuron Disease
Interventions
Acamprosate calcium
Ages
adults, older adults
Registry
NCT07204977

From the registry

Background: Amyotrophic lateral sclerosis (ALS) is a disorder that damages nerve cells in the brain and spinal cord. It can cause muscle weakness, paralysis, and loss of movement. The symptoms grow worse over time. Half of all people with ALS live only 3 to 5 years after diagnosis. Current drug treatments can slow the progress of the disease, but they cannot stop or reverse it. Objective: To test a study drug (acamprosate) in people with ALS with a mutation in the C9orf72 gene. Eligibility: People aged 18 years and older with ALS. They must have a mutation in the C9orf72 gene. Design: Participants will have 13 visits over 32 weeks. Five visits will be at the clinic, and 8 visits will be by phone. Participants will have a baseline visit of up to 3 days. They will have a physical exam with blood tests. They will have imaging scans and tests of their breathing ability. Their memory, thinking, and behavior will be assessed. They will have a neurologic exam to check their reflexes, strength, balance, eyes, and coordination. They will complete questionnaires about their daily…

Primary outcomes

  • Safety of acamprosate in patients with ALS and mutation in C9orf72.
Full record on ClinicalTrials.gov