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THRX > SEC Filings for THRX > Form 8-K on 24-Mar-2014All Recent SEC Filings

Show all filings for THERAVANCE INC



Regulation FD Disclosure

Item 7.01 Regulation FD Disclosure.

The information contained in this Item 7.01 shall not be deemed filed for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the "Securities Exchange Act of 1934"), or incorporated by reference in any filing under the Securities Exchange Act of 1934 or the Securities Act of 1933, as amended, except as shall be expressly set forth by specific reference in such filing.

GlaxoSmithKline plc (GSK) is scheduled to present data from a Phase 3 study, "Efficacy and Safety of Once-Daily Fluticasone Furoate/Vilanterol (FF/VI) and FF Over 12 Weeks In Patients With Persistent Asthma," and the protocol of the Phase 3 Salford Lung Study of FF/VI in asthma at the American Thoracic Society (ATS) 2014 International Conference held in San Diego, California from May 16-21, 2014. In addition, GSK is scheduled to present data from a Phase 1 concentration QT analysis study and post-hoc data analyses from Phase 3 studies of umeclidinium/vilanterol (UMEC/VI). BREO® ELLIPTA® is the proprietary name in the United States (U.S.) and Canada for FF/VI. RELVAR® ELLIPTA® is the proprietary name for FF/VI outside of the U.S. and Canada. RELVAR®/BREO® ELLIPTA® is a combination of the inhaled corticosteroid, FF, and the long-acting beta2-agonist (LABA), VI, in a single inhaler. ANORO™ ELLIPTA™ is the proprietary name for UMEC/VI. ANORO™ ELLIPTA™ is a combination of two bronchodilators, a LABA and an anticholinergic in a single inhaler. UMEC/VI and FF/VI have been developed under the 2002 LABA collaboration between GSK and Theravance, Inc. Titles and abstracts of poster presentations can be found in the Program Itinerary section of the ATS 2014 conference website

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