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GFF MDI (PT003)

DRUG6 trials

Sponsors

Pearl Therapeutics, Inc.

Conditions

COPDChronic Obstructive Pulmonary DiseaseChronic Obstructive Pulmonary Disease (COPD)

Phase 3

Multi-Center Study to Assess the Efficacy and Safety of PT003, PT005, and PT001 in Subjects With Moderate to Very Severe COPD (PINNACLE 2)
CompletedNCT01854658
Pearl Therapeutics, Inc.Chronic Obstructive Pulmonary Disease (COPD)
Start: 2013-07-31End: 2015-03-31Updated: 2017-03-28
Study to Assess the Efficacy and Safety of PT003, PT005, and PT001 in Subjects With Moderate to Very Severe COPD
CompletedNCT02343458
Pearl Therapeutics, Inc.Chronic Obstructive Pulmonary Disease
Start: 2015-03-30End: 2017-08-31Updated: 2019-02-20
24-hour Lung Function in Subjects With Moderate to Very Severe COPD After Treatment With PT003, Open-Label Spiriva® Respimat® as an Active Control, and Placebo
CompletedNCT02347072
Pearl Therapeutics, Inc.COPD
Start: 2015-02-01End: 2016-03-01Updated: 2017-04-19
24-hour Lung Function in Subjects With Moderate to Very Severe COPD After Treatment With PT003 and Placebo MDI
CompletedNCT02347085
Pearl Therapeutics, Inc.COPD
Start: 2015-02-01End: 2015-06-01Updated: 2018-07-19
Study to Evaluate the Treatment Effect of PT003 on Cardiovascular Hemodynamics in Subjects With Moderate to Severe COPD
TerminatedNCT02685293
Pearl Therapeutics, Inc.COPD
Start: 2016-12-09End: 2018-06-06Updated: 2019-08-28
Study to Assess the Safety and Efficacy of PT010, PT003, and PT009 in Japanese Subjects With COPD Compared With Symbicort® Turbohaler®
CompletedNCT03262012
Pearl Therapeutics, Inc.COPD
Start: 2016-08-09End: 2018-06-15Updated: 2020-05-13

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Benefits of glycopyrrolate/formoterol fumarate metered dose inhaler (GFF MDI) in improving lung function and reducing exacerbations in patients with moderate-to-very severe COPD: a pooled analysis of the PINNACLE studies.
2020-05-254 citations
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