A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Masupirdine (SUVN-502) for the Treatment of Agitation in Participants With Dementia of the Alzheimer's Type
Latest Information Update: 27 May 2025
At a glance
- Drugs Masupirdine (Primary)
- Indications Alzheimer's disease
- Focus Registrational; Therapeutic Use
- Sponsors Suven Life Sciences
Most Recent Events
- 20 May 2025 Planned End Date changed from 1 Jan 2025 to 1 Dec 2025.
- 20 May 2025 Planned primary completion date changed from 1 Jan 2025 to 1 Dec 2025.
- 20 Jul 2023 The subject enrolment is expected to be completed by Q3 2024, as per trial design, presented at the Alzheimer's Association International Conference 2023