INNOVIVA,INC. (NASDAQ:INVA) Files An 8-K Other EventsItem 8.01 Other Events.
On September19, 2017, GlaxoSmithKline plc (“GSK”) and Innoviva,Inc. (Innoviva) distributed a press release announced positive headline results from the phase III InforMing the PAthway of COPD Treatment (IMPACT) study of Trelegy Ellipta, the first and only once-daily single inhaler triple therapy comprising an inhaled corticosteroid (ICS), long-acting muscarinic antagonist (LAMA) and long-action beta agonist (LABA) approved by the U.S. Food and Drug Administration (“FDA”).
Trelegy Ellipta (fluticasone furoate/umeclidinium/vilanterol, FF/UMEC/VI) is approved by the FDA for the long-term, once-daily, maintenance treatment of patients with chronic obstructive pulmonary disease, including chronic bronchitis and/or emphysema, who are on a fixed-dose combination of fluticasone furoate and vilanterol for airflow obstruction and reducing exacerbations, in whom additional treatment of airflow obstruction is desired or patients who are on umeclidinium and a fixed-dose combination of fluticasone furoate and vilanterol.
The press release is filed as Exhibit99.1 to this report and is incorporated herein by reference.
Item 9.01.Financial Statements and Exhibits.
(d)Exhibits
99.1 |
Press Release dated September19, 2017 |