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Zervimesine - Cognition Therapeutics

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Drug Profile

Zervimesine - Cognition Therapeutics

Alternative Names: CT-1812; Elayta

Latest Information Update: 27 Aug 2025

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At a glance

  • Originator Cognition Therapeutics
  • Developer Alzheimers Clinical Trials Consortium; Cognition Therapeutics
  • Class Antidementias; Antiparkinsonians; Eye disorder therapies; Isoindoles; Neuroprotectants; Nootropics; Phenols; Small molecules; Sulfones
  • Mechanism of Action Sigma-2 receptor antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Phase II Alzheimer's disease; Dementia; Dry age-related macular degeneration
  • Preclinical Parkinson's disease
  • Discontinued Cognition disorders

Most Recent Events

  • 12 Aug 2025 Cognition Therapeutics expects receiving the US FDA’s minutes from end-of-Phase II meeting regarding registrational plans for zervimesine in Alzheimer’s disease in August 2025
  • 12 Aug 2025 Cognition Therapeutics receives the US FDA’s minutes from end-of-phase II meeting regarding registrational plans for zervimesine in Alzheimer’s disease
  • 07 Aug 2025 Zervimesine is available for licensing as of 07 Aug 2025

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