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FDA panel recommends approval of Glaxo/Theravance lung drug

Wed, 17th Apr 2013 18:34

April 17 (Reuters) - An advisory panel to the U.S. Food andDrug Administration recommended on Wednesday that the agencyapprove an experimental treatment for smoking-related lungdamage made by GlaxoSmithKline Plc and Theravance Inc.

The drug, Breo, is an inhaled treatment for chronicobstructive pulmonary disease (COPD), a condition that includesemphysema, chronic bronchitis or both. COPD is the third-leadingcause of death in the United States, according to federal data.

Analysts were expecting a favorable review based on the FDAstaff review, which was posted to the FDA's website on Monday. (Reporting By Toni Clarke in Washington; Editing by Gerald E.McCormick)

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