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New Data on SEROQUEL XR(TM) in Treatment of Both Major Depressive Disorder and Generalized Anxiety Disorder Presented at APA Annual Meeting
Date:5/5/2008

il to achieve a satisfactory response.(6,7) GAD affects about 6.8 million adults in the U.S., with women twice as likely to develop it compared to men, and approximately 30% of patients do not achieve an adequate response to short-term treatment.(8-10) AstraZeneca has investigated the use of SEROQUEL XR, an atypical antipsychotic, in the treatment of MDD as well as GAD, aiming to develop another potential treatment option for patients.

SEROQUEL XR MDD Clinical Studies

In the SEROQUEL XR clinical development program in MDD, short-term monotherapy studies (Studies 1, 2, 3, and 4) and short-term adjunct therapy studies (Studies 6 and 7) used the change in Montgomery-Asberg Depression Rating Scale (MADRS)* scores as the primary assessment of depression symptoms. In the long-term study (Study 5), the primary assessment was time to a depressed event using criteria including the MADRS. Doses of 50 mg, 150 mg and 300 mg of SEROQUEL XR were studied in the MDD program.(11)

"New MDD therapy options are clearly needed. Studies have shown that at least one-third of MDD patients who are treated with antidepressants fail to achieve a satisfactory response," said Dr. Richard Weisler, Adjunct Professor of Psychiatry at University of North Carolina School of Medicine, Adjunct Assistant Professor at Duke University Medical Center and lead investigator on the MDD short-term monotherapy study presented today. "Additionally, for those patients who do achieve a response from treatment with antidepressants, it may often take a few weeks of treatment before a benefit is seen. In the short- term monotherapy study presented today at APA, patients taking SEROQUEL XR had a significant improvement in depressive symptom scores as early as the fourth day of treatment compared with patients taking placebo."

The following MDD studies were presented at the APA meeting:

-- Study 1 (Poster # NR3-101) -- In a six-week, multicenter, double-blind

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SOURCE AstraZeneca
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