Last updated: 11/07/2018 12:11:52
Additional Analysis of Two Multicenter Trials Comparing the Efficacy and Safety of GSK573719/GW642444 with GSK573719, GW642444 and Tiotropium over 24 weeks in Subjects with COPD
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Additional Analysis of Two Multicenter Trials Comparing the Efficacy and Safety of GSK573719/GW642444 with GSK573719, GW642444 and Tiotropium over 24 weeks in Subjects with COPD
Trial description: Additional Analysis of Two Multicenter Trials Comparing the Efficacy and Safety of GSK573719/GW642444 with GSK573719, GW642444 and Tiotropium over 24 weeks in Subjects with COPD
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
DeCramer M, Anzueto A, Kerwin E, Kaelin T, Richard N, Crater G, Tabberer M, Harris S, Church A.Two multicentre randomised trials comparing the efficacy and safety of UMEC/VI with UMEC, VI or tiotropium over 24 weeks in subjects with COPD.Lancet Respir Med.2014;2(6):472-86
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2014-20-01
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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