H. Lundbeck starts clinical phase III study with Lu AA21004 in Japan
This randomized, double-blind and multi-center phase III clinical trial is expected to enroll approximately 360 patients with MDD and will evaluate the efficacy and safety of Lu AA21004 (5 and 10 mg) compared to placebo. Primary endpoint is change of MADRS total score from baseline after eight weeks.
Lu AA21004 is a structurally novel compound that is different from currently available antidepressants. Data from clinical trials conducted outside Japan have shown encouraging results for the potential efficacy and the tolerability profile of Lu AA21004. In addition to the Japanese study, the ongoing clinical trial programme includes four ongoing short-term studies and two long-term safety studies.
Lundbeck and Takeda will continuously work in collaboration to develop Lu AA21004 in order to provide the drug as soon as possible as a novel treatment with patients suffering from depression.
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