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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

Trial Profile

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

Status: Recruiting
Phase of Trial: Phase III

Latest Information Update: 27 May 2025

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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

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