Found 8 matching trials
24-hour Lung Function in Subjects With Moderate to Very Severe COPD After Treatment With PT003 and Placebo MDI PHASE3 Randomized, Phase IIIb, Two-period, Two-treatment Double-blind, Multi-cente...
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Pharmacokinetics and Safety Study of PT010 and PT003 in Healthy Chinese Adult Subjects PHASE1 A study to assess the pharmacokinetics and safety of two doses of PT010 and...
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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 PHASE3 Randomized, Phase IIIb, Three-period, Three-treatment, Double-blind, Multi-...
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Multiple Locations
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Phase I Study Evaluating the Safety and Pharmacokinetics of Budesonide, Glycopyrronium, and Formoterol Fumarate Inhalation Aerosol (BGF MDI) in Healthy Volunteers PHASE1 This is a Phase I, Randomized, Double-Blind Within Device, Single-Dose, Fou...
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Pearl Therapeutics Study Site
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PK Study of PT003 and PT001 in Japanese Healthy Subjects PHASE1 A Randomized, Double-Blind, Single-Dose, Four-Period, Four-Treatment, Cross...
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Glycopyrronium and Formoterol Fumarate (GFF) Metered Dose Inhaler (MDI) Dose Indicator Study in Adults With Moderate to Very Severe COPD PHASE3 This is an open-label, multi-center study to evaluate the accuracy, reliabi...
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Pearl Investigative Site
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Study to Assess the Efficacy and Safety of PT003, PT005, and PT001 in Subjects With Moderate to Very Severe COPD PHASE3 A chronic dosing (24 weeks) study to assess the efficacy and safety GFF MDI...
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Efficacy and Safety of PT003, PT005, and PT001 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD); (PINNACLE 1) PHASE3 The overall objective of this study is to assess the efficacy and safety of...
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Pearl Investigative Site
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