Glycopyrrolate/Formoterol Fumarate MDI Compared With Spiriva® as An Active Control in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
Completed · Phase 2
Conditions studied: Chronic Obstructive Pulmonary Disease
In brief
The primary objective of this study is to assess the efficacy of Glycopyrrolate/Formoterol Fumarate MDI relative to individual components (GP MDI and FF MDI) in subjects with moderate to severe COPD
Key facts
- Study ID
- NCT01587079
- Run by
- Pearl Therapeutics, Inc.
- People needed
- 159
- Starts
- 2012-04-01
- Expected to finish
- 2012-10-01
- Last updated by the study team
- 2016-06-30
Who can join
Age: 40 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Pearl Investigative Site — Glendale, Arizona, United States
- Pearl Investigative Site — Rancho Mirage, California, United States
- Pearl Investigative Site — Waterbury, Connecticut, United States
- Pearl Investigative Site — Clearwater, Florida, United States
- Pearl Investigative Site — Clearwater, Florida, United States
- Pearl Investigative Site — Pensacola, Florida, United States
- Pearl Investigative Site — Winter Park, Florida, United States
- Pearl Investigative Site — Lafayette, Louisiana, United States
- Pearl Investigative Site — North Dartmouth, Massachusetts, United States
- Pearl Investigative Site — Fridley, Minnesota, United States
- Pearl Investigative Site — St Louis, Missouri, United States
- Pearl Investigative Site — Summit, New Jersey, United States
- Pearl Investigative Site — Cincinnati, Ohio, United States
- Pearl Investigative Site — Medford, Oregon, United States
- Pearl Investigative Site — Medford, Oregon, United States
- Pearl Investigative Site — Rock Hill, South Carolina, United States
- Pearl Investigative Site — Spartanburg, South Carolina, United States
- Pearl Investigative Site — San Antonio, Texas, United States
- Pearl Investigative Site — Morgantown, West Virginia, United States
Full record on ClinicalTrials.gov
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