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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