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Wednesday, February 19, 2020

FDA Ad Com set for mortality reduction claim for Glaxo’s Trelegy Ellipta

An FDA advisory committee will meet on Tuesday, April 21, to review and discuss GlaxoSmithKline’s (NYSE:GSK) application seeking a mortality risk reduction claim for COPD inhalation therapy Trelegy Ellipta (fluticasone furoate, umeclidinium, & vilanterol).
The company in-licensed the product from Innoviva (NASDAQ:INVA) (formerly Theravance).

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