Ziprasidone 80 mg/day and 160 mg/day in the acute exacerbation of schizophrenia and schizoaffective disorder: a 6-week placebo-controlled trial. Ziprasidone Study Group

• Published in: Neuropsychopharmacology (New York, N.Y.) Vol. 20; no. 5; p. 491
• Main Authors: Daniel, D G, Zimbroff, D L, Potkin, S G, Reeves, K R, Harrigan, E P, Lakshminarayanan, M
• Format: Journal Article
• Language: English
• Published: England 01-05-1999
• Subjects: Acute Disease; Adolescent; Adult; Aged; Antipsychotic Agents - administration & dosage; Antipsychotic Agents - adverse effects; Antipsychotic Agents - therapeutic use; Double-Blind Method; Female; Humans; Male; Middle Aged; Piperazines - administration & dosage; Piperazines - adverse effects; Piperazines - therapeutic use; Psychotic Disorders - drug therapy; Psychotic Disorders - psychology; Schizophrenia - drug therapy; Schizophrenic Psychology; Thiazoles - administration & dosage; Thiazoles - adverse effects; Thiazoles - therapeutic use
• ISSN: 0893-133X

In this double-blind study, patients with an acute exacerbation of schizophrenia or schizoaffective disorder were randomized to receive either ziprasidone 80 mg/day (n = 106) or 160 mg/day (n = 104) or placebo (n = 92), for 6 weeks. Both doses of ziprasidone were statistically significantly more effective than placebo in improving the PANSS total, BPRS total, BPRS core items, CGI-S, and PANSS negative subscale scores (p < .05). Ziprasidone 160 mg/day significantly improved depressive symptoms in patients with clinically significant depression at baseline (MADRS > or = 14, over-all mean 23.5) (p < .05) as compared with placebo. The percentage of patients experiencing adverse events was similar in each treatment group, and resultant discontinuation was rare. The most frequent adverse events associated with ziprasidone were generally mild dyspepsia, nausea, dizziness, and transient somnolence. Ziprasidone was shown to have a very low liability for inducing movement disorders and weight gain. The results indicate that ziprasidone is effective and well tolerated in the treatment of the positive, negative, and depressive symptoms of an acute exacerbation of schizophrenia or schizoaffective disorder.