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FDA approves Vraylar for schizophrenia and bipolar disorder

21 September 2015  •  Author: Victoria White

Allergan and Gedeon Richter have announced that the US Food and Drug Administration (FDA) has approved Vraylar (cariprazine) capsules for the acute treatment of manic or mixed episodes associated with bipolar I disorder and for treatment of schizophrenia in adults.

vraylar

“We are pleased with the FDA approval of Vraylar, which represents an important new treatment option for adults living with bipolar I disorder and schizophrenia to help address the unmet medical needs of people with these complex conditions,” said David Nicholson, Executive Vice President and President of Global R&D brands of Allergan. “This approval reinforces our deep commitment to the mental health community, as we continue to build our robust CNS portfolio.”

Bipolar I disorder and schizophrenia are chronic and disabling mental health disorders. Bipolar I disorder, also known as manic-depressive illness, is a disorder of the brain that is characterized by fluctuations in mood, energy, activity levels, and the ability to carry out day-to-day tasks. Schizophrenia is characterised by delusions, hallucinations, disorganized speech and behaviour, and other symptoms that cause social or occupational dysfunction.

“Bipolar I disorder and schizophrenia are serious, chronic and treatable conditions. The symptoms and response to treatment vary from patient to patient making these conditions challenging to manage,” said Gary Sachs, MD, Founding Director of the Bipolar Clinic and Research Programme at the Massachusetts General Hospital and Associate Professor of Psychiatry at Harvard Medical School.

FDA approval of Vraylar based on trials involving more than 2,700 adults

The FDA approval of Vraylar is based on the results of three 3-week controlled trials in adults with manic or mixed episodes of bipolar I disorder and three 6-week placebo-controlled trials in adults with schizophrenia. In these clinical trials involving more than 2,700 adults, Vraylar demonstrated improvement compared to placebo as measured by Young Mania Rating Scale (YMRS) total scores in patients with bipolar mania and by Positive and Negative Syndrome Scale (PANSS) total scores in patients with schizophrenia. Vraylar also demonstrated efficacy as measured by the Clinical Global Impressions-Severity (CGI-S) rating scale, the secondary efficacy endpoints for both conditions.

“This approval is a notable achievement for Gedeon Richter’s discovery platform,” said Erik Bogsch, Managing Director of Richter Gedeon Plc. “Despite the variety of treatments available for the millions living with bipolar I disorder and schizophrenia, unmet needs remain and we are proud to offer an additional option to help patients manage their symptoms.”

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