Sixty clinically stable individuals with DSM-IV-diagnosed schizophrenia were enrolled in a four-week, multicenter, double-blind, placebo-controlled trial. They were randomized to receive either MK-0777 3 mg b.i.d., MK-0777 8 mg b.i.d, or a placebo. Each subject's cognition was evaluated at the start of the study and four weeks later. Cognitive outcomes for the three groups were compared.