A Phase 2a, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate Safety, Tolerability, Pharmacodynamic Markers, and Pharmacokinetics of AP-101 in Patients With Familial Amyotrophic Lateral Sclerosis (fALS) and Sporadic Amyotrophic Lateral Sclerosis (sALS)
Latest Information Update: 27 May 2025
At a glance
- Drugs AP 101 (Primary)
- Indications Amyotrophic lateral sclerosis
- Focus Adverse reactions
- Sponsors AL-S Pharma
Most Recent Events
- 20 May 2025 Planned End Date changed from 26 Oct 2025 to 15 Aug 2025.
- 20 May 2025 Planned primary completion date changed from 28 Dec 2024 to 15 Aug 2025.
- 27 Jun 2024 The protocol has been amended to increase in time frame for study primary endpoint (Number of Participants With Adverse Events (AEs) and Serious AEs (SAEs).