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Tideglusib for the Treatment of Amyotrophic Lateral Sclerosis
Sponsor: University of Zurich
Summary
Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative condition, mainly characterized by progressive weakness and wasting of the limbs, the respiratory and bulbar muscles. Respiratory insufficiency leads to a fatal outcome after a mean diseases duration of only three to five years. The disease is characterized by pathological accumulations of a protein called TDP-43, which can be found large cortical and sub-cortical areas of post-mortem ALS brains. No causal treatment for this condition is known to date, and there is a large unmet need to develop new strategies in order to halt or slow down its progression. The aim of this study is to test the safety and tolerability of Tideglusib, a treatment that is already in clinical trials for other neuromuscular conditions, in patients with ALS. It is assumed that this drug may have a significant therapeutic benefit in this population due to his mode of action: In the ALS mouse model, Tideglusib decreases significantly the amount of accumulated TDP-43 proteins within the cells.
Official title: Tideglusib for the Treatment of Amyotrophic Lateral Sclerosis (TIDALS): a Randomized Placebo-controlled Phase II Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
98
Start Date
2025-12-01
Completion Date
2026-03-01
Last Updated
2025-01-28
Healthy Volunteers
No
Conditions
Interventions
Tideglusib
1000 mg/day per os
Locations (5)
University Hospital Bern
Bern, Switzerland
University Hospital Geneva
Geneva, Switzerland
University Hospital Lausanne
Lausanne, Switzerland
Kantonsspital St. Gallen
Sankt Gallen, Switzerland
University Hospital Zurich
Zurich, Switzerland