CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 3,109 enrolled
Drug / intervention
FF/UMEC/VI +4 moredrug
Likely dose
FF/UMEC/VI 100 mcgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03467425
NCT03467425Phase 4Completed

The Clinical Effectiveness of Fluticasone Furoate/Umeclidinium Bromide/Vilanterol in a Single Inhaler (TRELEGY™ ELLIPTA™) When Compared With Non-ELLIPTA Multiple Inhaler Triple Therapies in COPD Patients Within a Usual Care Setting

GlaxoSmithKline·interventional·Posted Mar 16, 2018·Updated Sep 7, 2020

In Brief

A Phase 4 clinical trial evaluating FF/UMEC/VI, Inhaled Corticosteroid, and 3 other interventions for Pulmonary Disease, Chronic Obstructive. Completed, enrolled 3,109 participants across 143 sites in 5 countries.

Detailed Summary

The primary purpose of this study is to assess the effectiveness of TRELEGY ELLIPTA relative to non-ELLIPTA Multiple Inhaler Triple Therapies (MITT) for Chronic Obstructive Pulmonary Disease (COPD) control within the usual clinical practice setting. The study will be conducted once TRELEGY ELLIPTA has been approved in the countries in which the study will be conducted and is available commercially. This is a randomized, open-label, effectiveness, phase 4 study of 24 weeks' duration in COPD subjects to evaluate TRELEGY ELLIPTA (fluticasone furoate \[FF\]/vilanterol \[VI\]/umeclidinium bromide \[UMEC\]: 100 microgram \[mcg\]/62.5 mcg/25 mcg) inhalation powder taken once daily using a single ELLIPTA inhaler compared with any non-ELLIPTA MITT in the usual care setting. Effectiveness of TRELEGY ELLIPTA will be assessed by comparing proportion of COPD Assessment Test (CAT) responders at Week 24 between two treatment groups. TRELEGY and ELLIPTA are trademarks of GlaxoSmithKline (GSK) group of companies. The study will enroll approximately 3000 subjects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany, Netherlands, Spain, Sweden, United Kingdom
Collaborators--

Timeline

Phase 4CompletedFinished
201820192020202120222023202420252026
First PostedMar 16, 2018
Enrollment StartApr 11, 2018
Primary CompletionOct 10, 2019
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 8.3 years ago

Interventions

FF/UMEC/VIdrug

FF is a dry white powder containing 100 mcg GW685698 blended with lactose in one blister in the first strip of the DPI. UMEC/VI is a dry white powder containing 62.5 mcg of UMEC and 25 mcg of VI per blister, both blended together with lactose and magnesium stearate in the second strip of the DPI.

Inhaled Corticosteroiddrug

Inhaled Corticosteroid (ICS) as prescribed by the physician.

LAMAdrug

LAMA as prescribed by the physician.

LABAdrug

LABA as prescribed by the physician.

COPD rescue medicationsdrug

Rescue medications for COPD will be prescribed and obtained according to usual practice.