U.S. FDA approves dual-chamber syringe for Abilify Maintena (aripiprazole) extended-release injectable suspension for the treatment of schizophrenia

FDA

Otsuka Pharmaceutical Development & Commercialization, Inc. (Otsuka) and Lundbeck announced today that the U.S. Food and Drug Administration (FDA) has approved a new formulation of Abilify Maintena (aripiprazole) for extended-release injectable suspension – a pre-filled dual-chamber syringe. Abilify Maintena is an atypical antipsychotic indicated for the treatment of schizophrenia; efficacy was demonstrated in a placebo-controlled, randomized-withdrawal maintenance trial in patients with schizophrenia and additional support for efficacy was derived from oral aripiprazole trials. The companies expect the dual-chamber syringe will be available in the U.S. in January 2015.

For more details, go to: http://www.otsuka-us.com/newsroom/Pages/NewsArticle.aspx?ItemId=10

Michael Wonder

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Michael Wonder

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