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Interventional, Randomized, Double-blind, Parallel-group, Placebo-controlled, Multi-centre Study to Assess the Efficacy, Safety and Tolerability of Lu AF82422 in Patients With Multiple System Atrophy

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Trial Profile

Interventional, Randomized, Double-blind, Parallel-group, Placebo-controlled, Multi-centre Study to Assess the Efficacy, Safety and Tolerability of Lu AF82422 in Patients With Multiple System Atrophy

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 25 Sep 2024

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At a glance

  • Drugs Lu AF82422 (Primary)
  • Indications Multiple system atrophy
  • Focus Proof of concept; Therapeutic Use
  • Acronyms AMULET
  • Sponsors Lundbeck A/S

    • Most Recent Events

    • 14 Jun 2024 Planned End Date changed from 14 Feb 2025 to 14 May 2026.
    • 05 Mar 2024 Primary endpoint (Change From Baseline in the Unified Multiple System Atrophy Rating Scale (UMSARS) Part I and Part II Total Score (UMSARS TS) at the End of Treatment (EOT) DBP) has not been met as per results presented in Lundbeck A/S media release
    • 05 Mar 2024 According to a Lundbeck A/S media release, data from this trial will be presented at the International Conference on Alzheimers and Parkinsons Diseases and related neurological disorders (AD/PD 2024)

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