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NCT01017952 · ClinicalTrials.gov registry record · Phase 3
A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 3 study, sponsored by GlaxoSmithKline.
- Completed
- Registry status
- Phase 3
- Development phase
- 1,635
- Enrollment target
NCT01017952 is a Phase 3 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 1,635 participants.
The verdict
NCT01017952, a Phase 3 study, has completed, sponsored by GlaxoSmithKline.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 1,635 participants
- Enrollment target
Study Summary
The Purpose of this study is to assess the efficacy and safety of three strengths of the FF/GW642444 Inhalation Powder in subject with Chronic Obstructive Pulmonary Disease (COPD)
Interventions
- DRUG FF/GW642444 Inhalation Powder
- DRUG GW642444 Inhalation Powder
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,635 participants |
| Start Date | 2009-09-25 |
| Est. Completion | 2011-10-17 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01017952
The ClinicalTrials.gov registry entry for NCT01017952 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 1,635 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which FF/GW642444 Inhalation Powder is the first listed.
NCT01017952 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01017952 about?
NCT01017952 is a clinical study titled "A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)". The Purpose of this study is to assess the efficacy and safety of three strengths of the FF/GW642444 Inhalation Powder in subject with Chronic Obstructive Pulmonary Disease (COPD)
What is the current status of trial NCT01017952?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,635 participants. The study started on 2009-09-25. Estimated completion is 2011-10-17.
What interventions are being tested in trial NCT01017952?
The interventions under investigation include: FF/GW642444 Inhalation Powder (DRUG), GW642444 Inhalation Powder (DRUG).
Who is sponsoring clinical trial NCT01017952?
This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.
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