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ABSTRACT: Context
Amyloid-beta peptide (Abeta(42)) has been implicated in the pathogenesis of Alzheimer disease (AD). Tarenflurbil, a selective Abeta(42)-lowering agent, demonstrated encouraging results on cognitive and functional outcomes among mildly affected patients in an earlier phase 2 trial.Objective
To determine the efficacy, safety, and tolerability of tarenflurbil.Design, setting, and patients
A multicenter, randomized, double-blind, placebo-controlled trial enrolling patients with mild AD was conducted at 133 trial sites in the United States between February 21, 2005, and April 30, 2008. Concomitant treatment with cholinesterase inhibitors or memantine was permitted.Intervention
Tarenflurbil, 800 mg, or placebo, administered twice a day.Main outcome mea
SUBMITTER: Green RC
PROVIDER: S-EPMC2902875 | biostudies-literature | 2009 Dec
REPOSITORIES: biostudies-literature