We will develop AIT-082 for the treatment of dementia due to Alzheimer's disease, stroke or aging. In Phase I, we plan to complete the preclinical studies needed to submit an Investigational New Drug (IND) exemption application to the Food and Drug Administration (FDA). Specifically, we will: (1) determine the preclinical pharmacodynamics/pharmacokinetics of AIT-082, (2) conduct preclinical toxicological testing, and (3) conduct additional preclinical studies on the mechanism of action of AIT-082. The aim of Phase II will be to file an IND application and to establish the clinical safety and efficacy of AIT-082.Awardee's statement of the potential commercial applications of the research:AIT-082 has potential commercial application for the treatment of memory deficiencies associated with Alzheimer's disease, aging, stroke, infection with human immunodeficiency virus (HIV), electroconvulsive shock treatment (ECT) of depression and attention deficit disorder (ADD).National Institute on Aging (NIA)