Study to Evaluate DNL747 in Subjects With Amyotrophic Lateral Sclerosis
Stopped early · Phase 1 · Has a placebo group
Conditions studied: Amyotrophic Lateral Sclerosis
In brief
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of multiple oral doses of DNL747 in subjects with Amyotrophic Lateral Sclerosis in a cross-over design
Key facts
- Study ID
- NCT03757351
- Run by
- Sanofi
- People needed
- 15
- Starts
- 2018-12-14
- Expected to finish
- 2020-06-18
- Last updated by the study team
- 2025-09-22
Who can join
Age: 21 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Bioclinica — Orlando, Florida, United States
- PRA Health Sciences — Salt Lake City, Utah, United States
- CHDR — Leiden, South Holland, Netherlands
Full record on ClinicalTrials.gov
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