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Sarepta Soars On New FDA Duchenne Drug Panel

This article was originally published in Scrip

Executive Summary

Investors took a much sunnier view on March 10 of Sarepta Therapeutics Inc. – driving its stock up as high as 16% – after the FDA announced a new date for its Peripheral and Central Nervous System (PCNS) Advisory Committee to examine the company's new drug application (NDA) for its experimental Duchenne muscular dystrophy (DMD) drug eteplirsen.






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