Clinical Trial of CT1812 in Mild to Moderate Alzheimer's Disease

Status Completed

Clinical Trial Summary

This is a multi-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 28 days. This trial may include up to 8 qualified investigator sites in Australia.

Clinical Trial Description

Screening procedures will occur up to 42 days. Eligible subjects will randomized at the clinic on Day 1 and receive the first dose of study drug. Dosing for 28 days thereafter off-site and a total of 5 clinic visits over the treatment period for safety and lab assessments. Then a 7 day post-treatment completion follow-up visit (Day 35) and End of Study for last safety assessments (Day 49). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02907567
Study type	Interventional
Source	Cognition Therapeutics
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	September 2016
Completion date	September 2017

View Details

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