| Literature DB >> 28848898 |
Gary T Ferguson1, Angel Fowler Taylor2, Chau Thach2, Qian Wang3, Agnes A Schubert-Tennigkeit4, Francesco Patalano4, Donald Banerji2.
Abstract
Background: The objective of the FLIGHT3 study was to evaluate the long-term safety and efficacy of indacaterol/glycopyrrolate* (IND/GLY) versus an active comparator, IND, in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD) over 52 weeks. Method: FLIGHT3 was a multicenter, randomized, double-blind, parallel-group, 52-week study. Patients were randomized (1:1:1) to IND/GLY (27.5/15.6 or 27.5/31.2 µg twice daily [b.i.d.]) or IND (75 µg once daily [o.d.]), delivered via the Neohaler® device. The primary objective was to evaluate the long-term safety and tolerability of IND/GLY versus IND in terms of adverse event (AE)-reporting rates in patients with moderate-to-severe COPD over 52 weeks. The secondary objective was to evaluate the long-term efficacy of IND/GLY versus IND in terms of pre-dose trough forced expiratory volume in 1 second (FEV1) and post-dose 1-h FEV1 over 52 weeks.Entities:
Keywords: chronic obstructive pulmonary disease; clinical trials; copd; long-acting beta2-agonists; long-acting muscarinic antagonist
Year: 2016 PMID: 28848898 PMCID: PMC5556955 DOI: 10.15326/jcopdf.3.4.2016.0131
Source DB: PubMed Journal: Chronic Obstr Pulm Dis ISSN: 2372-952X