FDA panel recommends approval of Glaxo/Theravance lung drug
April 17 (Reuters) - An advisory panel to the U.S. Food and Drug Administration recommended on Wednesday that the agency approve an experimental treatment for smoking-related lung damage made by GlaxoSmithKline Plc and Theravance Inc .
The drug, Breo, is an inhaled treatment for chronic obstructive pulmonary disease (COPD), a condition that includes emphysema, chronic bronchitis or both. COPD is the third-leading cause of death in the United States, according to federal data.
Analysts were expecting a favorable review based on the FDA staff review, which was posted to the FDA's website on Monday. (Reporting By Toni Clarke in Washington; Editing by Gerald E. McCormick)
- North Korea's 'reign of terror' worries South's leader
- Google bus blocked in San Francisco gentrification protest
- Los Angeles sheriff's officials charged in jail misconduct probe
- Putin dissolves state news agency, tightens grip on Russia media
- Chinese hackers spied on Europeans before G20 meeting: researcher