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Aripiprazole, an Antipsychotic With a Novel Mechanism of Action, and Risperidone vs Placebo in Patients With Schizophrenia and Schizoaffective Disorder

2003; American Medical Association; Volume: 60; Issue: 7 Linguagem: Inglês

10.1001/archpsyc.60.7.681

1538-3636

Steven G. Potkin, Anutosh Ranjan Saha, Mary J. Kujawa, William H. Carson, Mirza W. Ali, Elyse Stock, Joseph Stringfellow, Г. Ингенито, Stephen R. Marder,

Neurotransmitter Receptor Influence on Behavior

Background: Aripiprazole is a dopamine D 2 receptor partial agonist with partial agonist activity at serotonin 5HT 1A receptors and antagonist activity at 5HT 2A receptors.This multicenter trial examined the efficacy, safety, and tolerability of aripiprazole in patients with acute exacerbation of schizophrenia or schizoaffective disorder.Methods: In this 4-week double-blind study, 404 patients were randomized to 20 mg/d (n=101) or 30 mg/d (n=101) of aripiprazole, placebo (n=103), or 6 mg/d of risperidone (n=99).Efficacy assessments included Positive and Negative Syndrome Scale (PANSS) scores and Clinical Global Impression scores.Safety and tolerability evaluations included extrapyramidal symptoms and effects on weight, prolactin, and corrected QT (QT c ) interval.Results: Aripiprazole (20 and 30 mg/d) and risperidone (6 mg/d) were significantly better than placebo on all efficacy measures.Separation from placebo occurred at week 1 for PANSS total and positive scores with aripiprazole and risperidone and for PANSS negative scores with aripiprazole.There were no significant differences between aripiprazole and placebo in mean change from baseline in the extrapyramidal symptom rating scales.Mean prolactin levels decreased with aripiprazole but significantly increased 5-fold with risperidone.Mean change in QT c interval did not differ significantly from placebo with any active treatment group.Aripiprazole and risperidone groups showed a similar low incidence of clinically significant weight gain.Conclusions: Aripiprazole is effective, safe, and well tolerated for the positive and negative symptoms in schizophrenia and schizoaffective disorder.It is the first non-D 2 receptor antagonist with clear antipsychotic effects and represents a novel treatment development for psychotic disorders.