CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 236 enrolled
Drug / intervention
UMEC/VI +2 moredrug
Likely dose
UMEC/VI 62.5/25 mcg once daily via ELLIPTA inhaler; TIO/OLO 2.5/2.5 mcg once daily (delivered as 3.124/2.736 mcg) via RESPIMAT inhalerAI-extracted
Key inclusion· 5
  • Age ≥40 years at baseline
  • Confirmed COPD diagnosis per ATS/ERS criteria
  • Current or former smoker with ≥10 pack-year history; former smokers must have quit ≥6 months prior
  • Airflow obstruction: pre- and post-albuterol FEV1/FVC <0.70 and post-albuterol FEV1 50-70% predicted
Key exclusion· 16
  • Current diagnosis of asthma
  • Alpha-1 antitrypsin deficiency as underlying cause of COPD
  • Active tuberculosis or other primary respiratory disorders (bronchiectasis, sarcoidosis, lung fibrosis, pulmonary hypertension, interstitial lung disease)
  • Any condition unlikely to survive study duration or rapidly progressing/life-threatening disease (e.g. cancer)

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

Search/NCT02799784
NCT02799784Phase 4Completed

A Randomized, Open-Label, 8-Week Cross-Over Study to Compare Umeclidinium/Vilanterol With Tiotropium/Olodaterol Once-Daily in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

GlaxoSmithKline·interventional·Posted Jun 15, 2016·Updated Jul 2, 2018

In Brief

A Phase 4 clinical trial evaluating UMEC/VI, TIO/OLO, and 1 other intervention for Pulmonary Disease, Chronic Obstructive. Completed, enrolled 236 participants across 35 sites in 4 countries.

Detailed Summary

The primary objective of this study is to assess the effect of umeclidinium/vilanterol (UMEC/VI) versus tiotropium/olodaterol (TIO/OLO) in subjects with moderated COPD. This is a multicentre, randomized, open label, 2 period crossover complete block design study. Eligible subjects, who complete a 2-week run-in period, will be randomized to receive a sequence consisting of UMEC/VI inhalation powder (62.5/25 microgram \[mcg\] once-daily \[QD\]) administered as 1 inhalation via the ELLIPTA® Inhaler and TIO/OLO 5/5 mcg inhalation spray administered as 2 inhalations via the RESPIMAT® inhaler, for 8 weeks each. This will be followed by a 3-week washout period and one-week follow-up period. The total duration of subject participation in the study will be approximately 22 weeks. ELLIPTA is a registered trademark of the GlaxoSmithKline group of companies. RESPIMAT is a registered trademark of Boehringer Ingelheim.

Study Details

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

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedJun 15, 2016
Enrollment StartJul 14, 2016
Primary CompletionApr 27, 2017
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 10.0 years ago

Interventions

UMEC/VIdrug

ELLIPTA dry powder inhaler (DPI) will contain a total of 30 doses. Each DPI will be comprised of two double-foil, laminate blister strips. Each blister of one strip will consist of 62.5 mcg of UMEC blended with lactose and magnesium stearate while each blister of other strip will consist of 25 mcg of VI blended with lactose and magnesium stearate. Each actuation of the DPI will deliver the contents of one blister from each strip simultaneously

TIO/OLOdrug

TIO/OLO inhalation spray will be supplied as an inhalation spray delivered using a RESPIMAT inhaler. Each actuation from the RESPIMAT inhaler delivers 3.124 mcg tiotropium bromide monohydrate (equivalent to 2.5 mcg tiotropium) and 2.736 mcg olodaterol hydrochloride (equivalent to 2.5 mcg olodaterol)

Albuterol/salbutamoldrug

Albuterol/salbutamol will be supplied as an inhalation spray via metered dose inhaler and will be issued for reversibility testing at Visit 1. Albuterol/salbutamol will be permitted throughout the study for use as-needed