CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 44 enrolled
Drug / intervention
GSK2269557 +3 moredrug
Likely dose
GSK2269557 500 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/NCT02522299
NCT02522299Phase 2Completed

A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Efficacy and Changes in Induced Sputum and Blood Biomarkers Following Daily Repeat Doses of Inhaled GSK2269557 for 12 Weeks in Adult Subjects Diagnosed With an Acute Exacerbation of Chronic Obstructive Pulmonary Disease (COPD)

GlaxoSmithKline·interventional·Posted Aug 13, 2015·Updated Sep 5, 2021

In Brief

A Phase 2 clinical trial evaluating GSK2269557, Placebo, and 2 other interventions for Pulmonary Disease, Chronic Obstructive. Completed, enrolled 44 participants across 6 sites in 2 countries.

Detailed Summary

The purpose of this study is to evaluate specific alterations in immune cell mechanisms related to neutrophil function as detected by PI3Kdelta-dependent changes in messenger ribonucleic acid (mRNA) extracted from induced sputum in patients experiencing an exacerbation of COPD, with or without treatment with GSK2269557. The efficacy of treatment with GSK2269557 will also be measured using functional respiratory imaging (FRI) and spirometry. This is a randomised, double-blind, placebo-controlled, parallel-group study. The study consisted of Screening Phase (up to 3 days prior to Day 1), Treatment Phase (Days 1 to 84) and Follow phase (7 to 14 days after last dose). The total duration of the study is 13-14 weeks including the screening visit. DISKUS TM and ELLIPTA TM are registered trademark of GSK group of companies.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Denmark
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedAug 13, 2015
Enrollment StartNov 4, 2015
Primary CompletionJun 15, 2018
Study CompletionJun 22, 2018
TodayJul 2, 2026
Enrollment to primary: 2.6 yearsPosted 10.9 years ago

Interventions

GSK2269557drug

GSK2269557 500 mcg blended with lactose per blister and will be administered using a DISKUS dry powder inhaler device. Since GSK2269557 will no longer be manufactured for use with the DISKUS device, it will be replaced with ELLIPTA Device. Subjects will receive GSK2269557 700 mcg once daily for 84 consecutive days via ELLIPTA.

Placebodrug

Lactose will be administered using a DISKUS and ELLIPTA dry powder inhaler device

DISKUSdevice

It is multi-dose dry powder inhaler containing one foil strip of drug with 60 blisters

ELLIPTAdevice

It is multi-dose dry powder inhaler containing one foil strip of drug with 30 blisters