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Dainippon Sumitomo Pharma and Takeda Pharmaceutical receive European Marketing Authorization for Latuda

Sunday, 30 Mar 2014 07:00pm EDT 

Dainippon Sumitomo Pharma Co Ltd and Takeda Pharmaceutical Co Ltd:Say European Commission has granted Marketing Authorization for once-daily oral Latuda for the treatment of schizophrenia in adults.The Marketing Authorization was based on a comprehensive clinical trial program of eight studies, which included placebo and active comparators. 

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