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NOT YET RECRUITING
NCT05105958
PHASE2

Tideglusib for the Treatment of Amyotrophic Lateral Sclerosis

Sponsor: University of Zurich

View on ClinicalTrials.gov

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

Interventions

DRUG

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