Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Randomized, Double-Blind, Placebo-Controlled, Phase I Study of the Safety & Pharmacokinetics of Two Doses of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease

Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Phase I Study of the Safety & Pharmacokinetics of Two Doses of CT1812 in Subjects With Mild to Moderate Alzheimer's Disease

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 12 Mar 2025

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Zervimesine (Primary)
  • Indications Alzheimer's disease
  • Focus Adverse reactions
  • Sponsors Cognition Therapeutics

Most Recent Events

  • 27 Feb 2025 According to a Cognition Therapeutics media release, the company has published a manuscript reviewing recent work with data from an unbiased pathway analysis of CSF proteomes from AD participants treated in this study which supports the potential of zervimesine (CT1812) in The Nature Journal, Scientific Reports.
  • 10 Feb 2021 Results presented in a Cognition Therapeutics media release.
  • 10 Feb 2021 According to a Cognition Therapeutics media release, biomarker findings from the study have been published in Alzheimer's & Dementia: The Journal of the Alzheimer's Association.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top