drugset / Trial / NCT00109564

A Safety and Efficacy Study of Ispronicline (TC-1734-112) in Subjects With Age Associated Memory Impairment (AAMI)

NCT00109564 ↗

Phase 2 Completed 174 enrolled Targacept Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this Phase II study is to evaluate the efficacy and safety of ispronicline (TC-1734-112) compared to placebo (inactive substance pill) in patients with age associated memory impairment (AAMI). AAMI is characterized as cognitive impairment including memory loss and poor concentration associated with aging.

Timeline

Start
2005-01
Primary completion
—
Completion
2005-10

Outcome

Met primary endpoint

paper As all three co-primary outcomes were positive it can be concluded the compound likely had a beneficial effect on cognition. PMID 20542923 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject ispronicline Small molecule 25 mg Oral
Subject ispronicline Small molecule 50 mg Oral

Indications