drugset / Trial / NCT01854645

Efficacy and Safety of PT003, PT005, and PT001 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD); (PINNACLE 1)

NCT01854645

Phase 3 Completed 2103 enrolled Pearl Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The overall objective of this study is to assess the efficacy and safety of treatment with PT003 (GFF MDI), PT005 (FF MDI), PT001 (GP MDI), and open-label tiotropium bromide inhalation powder compared with each other and Placebo MDI over 24 weeks in subjects with moderate to very severe COPD.

Timeline

Start
2013-05
Primary completion
2015-02
Completion
2015-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Formoterol Other / unclassified 9.6 ug Other
Subject Glycopyrrolate Small molecule 18 ug Other
Comparator Tiotropium Other / unclassified 18 ug Other