Pharmaceutical Business review

AstraZeneca files supplementary NDAs for treatment of bipolar disorder

The bipolar mania submission is based on a clinical study of once-daily treatment with Seroquel, compared to placebo, with a primary endpoint of change in YMRS (Young Mania Rating Scale) total score (week 3), in 316 patients suffering from bipolar mania. The bipolar depression submission is supported by a clinical study of once-daily treatment with Seroquel, compared to placebo, with a primary endpoint of change from baseline in MADRS (Montgomery Asberg Depression Rating Scale) total score after 8 weeks of treatment, in 280 patients diagnosed with bipolar depression.

Doses of Seroquel administered in both the bipolar mania (400mg to 800mg/day) and bipolar depression (30 mg/day) studies were comparable to the FDA-approved recommended doses for Seroquel (quetiapine fumarate) immediate release tablets in those indications. Both studies met their primary endpoint.

Seroquel is currently approved in 8 countries including the US, Canada and the Netherlands, for acute and maintenance treatment of schizophrenia in adults.