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Astellas Pharma’s Vernakalant For Atrial Fibrillation Goes Before FDA Panel

This article was originally published in The Pink Sheet Daily

Executive Summary

FDA’s Cardiovascular and Renal Drugs Advisory Committee considers Astellas’ NDA re-submission for the indication Dec. 11.

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Safety and efficacy of Cardiome/Astellas’ vernakalant and Solvay’s tedisamil will be debated during the Dec. 11-12 meeting, according to Cardiome.

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