GSK and Theravance file for FF/VI approval in the USA and Europe; Talks with … – The Pharma Letter

GSK and Theravance file for FF/VI approval in the USA and Europe; Talks with
The Pharma Letter
Asthma (100/25mcg and 200/25mcg): The regular treatment of asthma in adults and adolescents aged 12 years and older, where use of a combination product (long-acting beta2-agonist and inhaled corticosteroid) is appropriate. • COPD (100/25mcg): The
GSK, Theravance seek approvals for FF/VI in US, EuropePharmaceutical Business Review
GSK and Theravance file next-generation Advair in USA, EUPharma Times

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Letter: May is Asthma Awareness Month – Fond du Lac Reporter

Letter: May is Asthma Awareness Month
Fond du Lac Reporter
May is Asthma Awareness Month. Asthma is a serious, sometimes life-threatening disease and affects almost 20 million people in the United States. Every day in America, 40000 people miss school or work, 30000 people have an asthma attack,
May: Asthma Awareness MonthMilwaukee Courier Weekly Newspaper
Letter: Help asthma suffers: Keep smoke awayWausau Daily Herald

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Relovair COPD and asthma filings on track despite more mixed trial results – The Pharma Letter


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Relovair COPD and asthma filings on track despite more mixed trial results
The Pharma Letter
For asthma, the company plans to file for approval in Europe in mid-2012 and will continue discussions with the US Food and Drug Administration on the regulatory requirements for a US asthma indication. GSK is looking to replace its top-selling drug
Relovair on track for filing in mid-2012, says GSKPMLiVE
GSK, Theravance Report Mixed Bag of Data for Relovair in COPD, AsthmaGenetic Engineering News
GSK and Theravance Announce Completion of the Relovair(TM)* Registrational MarketWatch (press release)
Reuters –MedCity News –FierceBiotech
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