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Eisai Seeks Lunesta Approval In Japan After Phase III Data, But Disease Awareness Is A Challenge

This article was originally published in PharmAsia News

Executive Summary

TOKYO - Eisai announced Sept. 15 positive results from a Japanese Phase II/III efficacy study and a Phase III safety study for Lunesta (eszopiclone), giving the company adequate data to seek approval for the drug from Japan's Ministry of Health, Labor and Welfare in fiscal year 2010

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