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8-K Filing
Innoviva (INVA) 8-KOther Events
Filed: 11 Jun 14, 12:00am
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the |
Date of Report: June 11, 2014 (Date of earliest event reported) | ||||
Theravance, Inc. (Exact name of registrant as specified in its charter) | ||||
Delaware (State or other jurisdiction of incorporation) | 000-30319 (Commission File Number) | 94-3265960 (IRS Employer Identification Number) | ||
951 Gateway Boulevard, South San Francisco, CA (Address of principal executive offices) | 94080 (Zip Code) | |||
650-238-9600 (Registrant's telephone number, including area code) | ||||
Not Applicable (Former Name or Former Address, if changed since last report) |
Item 8.01. Other Events On June 11, 2014, GlaxoSmithKline plc (GSK) and Theravance, Inc. issued a press release announcing positive results from two Phase 3 studies which showed that patients with chronic obstructive pulmonary disease (COPD) who received the anticholinergic, INCRUSE(TM) ELLIPTA(R) (umeclidinium (UMEC) 62.5mcg), or umeclidinium 125mcg (an unlicensed dose) in addition to RELVAR(R)/BREO(R) ELLIPTA(R) (fluticasone furoate/vilanterol, "FF/VI"), an inhaled corticosteroid / long-acting beta2-agonist (LABA) combination, achieved an additional improvement in lung function (FEV1) compared to patients receiving FF/VI plus placebo. FF/VI has been developed under the LABA collaboration agreement between Glaxo Group Limited and Theravance, Inc. A copy of the press release is filed as Exhibit 99.1 to this report and is incorporated herein by reference. Item 9.01. Financial Statements and Exhibits (d) Exhibits 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. |
Dated: June 11, 2014 | THERAVANCE, INC. By: /s/ Michael W. Aguiar |
Exhibit No. | Description |
99.1 | Press Release dated June 11, 2014 |