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AC-1204 26-Week Long Term Efficacy Response Trial With Optional Open-label Ext


A 26-Week, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Effects of Daily Administration of AC-1204 in Participants With Mild to Moderate Alzheimer`s Disease (AD) With an Optional 26-Week Open Label Extension




This study will evaluate the effects of daily dosing of AC-1204 on cognition, activities of daily living, resource utilization, quality of life, pharmacokinetic measures and safety among participants with mild to moderate Alzheimer`s Disease.

Study Status: Recruiting


Condition Intervention Phase
Alzheimer`s Disease Drug: AC-1204
Drug: Placebo
Phase 2/Phase 3

Verified by Accera, Inc. January, 2014

Sponsored by: Accera, Inc.
Information provided by: Accera, Inc. identifier: NCT01741194

Study Type: Interventional

Study Design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care

Cleveland Clinic Lou Ruvo Center for Brain Health
Las Vegas, Nevada 89106
United States

Samuel T Henderson, PhD., Study Director

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