<SEC-DOCUMENT>0001102624-14-000426.txt : 20140324
<SEC-HEADER>0001102624-14-000426.hdr.sgml : 20140324
<ACCEPTANCE-DATETIME>20140324160524
ACCESSION NUMBER:		0001102624-14-000426
CONFORMED SUBMISSION TYPE:	8-K
PUBLIC DOCUMENT COUNT:		1
CONFORMED PERIOD OF REPORT:	20140324
ITEM INFORMATION:		Regulation FD Disclosure
FILED AS OF DATE:		20140324
DATE AS OF CHANGE:		20140324

FILER:

	COMPANY DATA:	
		COMPANY CONFORMED NAME:			THERAVANCE INC
		CENTRAL INDEX KEY:			0001080014
		STANDARD INDUSTRIAL CLASSIFICATION:	PHARMACEUTICAL PREPARATIONS [2834]
		IRS NUMBER:				943265960
		STATE OF INCORPORATION:			DE
		FISCAL YEAR END:			1231

	FILING VALUES:
		FORM TYPE:		8-K
		SEC ACT:		1934 Act
		SEC FILE NUMBER:	000-30319
		FILM NUMBER:		14713292

	BUSINESS ADDRESS:	
		STREET 1:		901 GATEWAY BLVD
		CITY:			SOUTH SAN FRANCISCO
		STATE:			CA
		ZIP:			94080
		BUSINESS PHONE:		6508086000

	MAIL ADDRESS:	
		STREET 1:		901 GATEWAY BLVD
		CITY:			S. SAN FRANCISCO
		STATE:			CA
		ZIP:			94080

	FORMER COMPANY:	
		FORMER CONFORMED NAME:	ADVANCED MEDICINE INC
		DATE OF NAME CHANGE:	20000302
</SEC-HEADER>
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<TYPE>8-K
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<FILENAME>theravance8k.htm
<DESCRIPTION>THERAVANCE, INC. 8-K
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<div style="TEXT-INDENT: 0pt; DISPLAY: block; MARGIN-LEFT: 0pt; MARGIN-RIGHT: 0pt" align="center"><font style="DISPLAY: inline; FONT-FAMILY: Times New Roman; FONT-SIZE: 10pt">Date of Report (Date of earliest event Reported):&#160;&#160;March 24, 2014</font></div>

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<div style="TEXT-INDENT: 0pt; DISPLAY: block; MARGIN-LEFT: 0pt; MARGIN-RIGHT: 0pt" align="left"><font style="DISPLAY: inline; FONT-FAMILY: Times New Roman; FONT-SIZE: 10pt">GlaxoSmithKline plc (GSK) is scheduled to present data from a Phase 3 study, &#8220;Efficacy and Safety of Once-Daily Fluticasone Furoate/Vilanterol (FF/VI) and FF Over 12 Weeks In Patients With Persistent Asthma,&#8221; 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.&#160;&#160;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).&#160;&#160;BREO<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font> ELLIPTA<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font> is the proprietary name in the United States (U.S.) and Canada for FF/VI.&#160;&#160;RELVAR<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font> ELLIPTA<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font> is the proprietary name for FF/VI outside of the U.S. and Canada.&#160;&#160;RELVAR<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font>/BREO<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font> ELLIPTA<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: text-top">&#174;</font> is a combination of the inhaled corticosteroid, FF, and the long-acting beta<font style="DISPLAY: inline; FONT-SIZE: 70%; VERTICAL-ALIGN: sub">2</font>-agonist (LABA), VI, in a single inhaler.&#160;&#160;ANORO&#8482; ELLIPTA&#8482; is the proprietary name for UMEC/VI.&#160;&#160;ANORO&#8482; ELLIPTA&#8482; is a combination of two bronchodilators, a LABA and an anticholinergic in a single inhaler.&#160;&#160;UMEC/VI and FF/VI have been developed under the 2002 LABA collaboration between GSK and Theravance, Inc.&#160;&#160;Titles and abstracts of poster presentations can be found in the Program Itinerary section of the ATS 2014 conference website <font style="DISPLAY: inline; TEXT-DECORATION: underline">https://cms.psav.com/cPaper2014/ats2014/myitinerary</font>.</font></div>

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<div style="TEXT-INDENT: 27pt; DISPLAY: block; MARGIN-LEFT: 0pt; MARGIN-RIGHT: 0pt" align="left"><font style="DISPLAY: inline; FONT-FAMILY: Times New Roman; FONT-SIZE: 10pt">Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.</font></div>

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