Schizophrenia :: Abilify sNDA for pediatric patients with schizophrenia accepted for priority FDA review
Otsuka Pharmaceutical Co, Ltd., and Bristol-Myers Squibb Company (NYSE: BMY) announced today that the U.S. Food and Drug Administration (FDA) has accepted for priority (six month review target) review the supplemental New Drug Application (sNDA) of the atypical antipsychotic ABILIFY? (aripiprazole) for the treatment of pediatric patients (13-17 years old) with schizophrenia.