Effect of CT1812 Treatment on Brain Synaptic Density

Status Completed

Clinical Trial Summary

Study to Evaluate the Safety and Tolerability of Oral CT1812 in Subjects with Mild to Moderate Alzheimer's Disease.

Clinical Trial Description

This is a single-center, randomized, double-blind, placebo-controlled, parallel group study of two doses of CT1812 in adults with mild to moderate Alzheimer's Disease to evaluate the safety and tolerability of oral CT1812, administered for up 180 days for the Primary study and another 180 days for the double-blind extension study. Each participant and caregiver participated in a screening period of up to 60 days, followed by the primary double-blind treatment period of 24 weeks (169 days +/-2) followed by an optional double-blind extension treatment period of another 24 weeks (337 days +/-2). ;

Study Design

Related Conditions & MeSH terms

Alzheimer Disease

Clinical Trial Details

NCT number	NCT03493282
Study type	Interventional
Source	Cognition Therapeutics
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	March 28, 2018
Completion date	October 16, 2020

View Details

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