Bipolar Depression Clinical Trial
Official title:
Asenapine for Bipolar Depression
The purpose of this study is to compare asenapine with placebo in the treatment of depression
associated with bipolar disorder, type I over eight weeks.
We hypothesize that patients will show significantly greater improvement with asenapine than
placebo over eight weeks of treatment.
86 patients with an episode of major depression associated with bipolar disorder, type I will be recruited by two sites for the study over fifteen months. Medication will be administered in a double-blind manner. Patients will receive asenapine (or placebo) beginning on day 0 at 5 mg bid. Dose may be increased to 10 mg bid and adjusted based on clinical response. Patients will be evaluated by a blinded (to treatment status) rater. Patients will be seen and ratings obtained at baseline (day 0) and on days 7, 14, 28, 42, and 56 (or termination from the study). Adverse events will be evaluated as well. ;
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