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Last Updated: November 17, 2024

CLINICAL TRIALS PROFILE FOR PERFOROMIST


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All Clinical Trials for perforomist

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00633776 ↗ Perforomist Versus Foradil Evaluated by Inspiratory Capacity and High Resolution Computed Tomography (HRCT) Withdrawn Dey, L.P. Phase 4 2008-03-01 The purpose of this study is to compare the effects of nebulized formoterol fumarate (Perforomist) to dry-powder inhaler formoterol fumarate (Foradil). Perforomist is a solution that is made into very fine spray (using a nebulizer) that is then breathed in over 10-15 minutes. Foradil is taken in a single quick, deep inhalation.
NCT00633776 ↗ Perforomist Versus Foradil Evaluated by Inspiratory Capacity and High Resolution Computed Tomography (HRCT) Withdrawn University of California, Los Angeles Phase 4 2008-03-01 The purpose of this study is to compare the effects of nebulized formoterol fumarate (Perforomist) to dry-powder inhaler formoterol fumarate (Foradil). Perforomist is a solution that is made into very fine spray (using a nebulizer) that is then breathed in over 10-15 minutes. Foradil is taken in a single quick, deep inhalation.
NCT01488019 ↗ Study to Evaluate the Safety of Long-Term Use of Perforomist® (Formoterol Fumarate) Completed Dey Phase 4 2012-03-01 This study is a multi-center, randomized, placebo-controlled study to evaluate the long-term safety of Perforomist® inhalation therapy in subjects with Chronic Obstructive Pulmonary Disease (COPD). Individual participation is approximately 54 weeks, including 52 weeks of double-blind treatment.
NCT02291016 ↗ COPD Aerosol Study Comparing the Efficacy of Nebulizers Versus Dry Powder Inhalers Completed Mylan Specialty L.P. N/A 2015-02-01 The purpose of this study is to compare drug delivery and lung function after treatment with formoterol from a nebulizer versus a dry powder inhaler (DPI) in patients recovering from severe exacerbations of COPD. This is to determine if one device is superior in providing better lung function and drug deposition in this clinical setting.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for perforomist

Condition Name

Condition Name for perforomist
Intervention Trials
Chronic Obstructive Pulmonary Disease (COPD) 2
COPD 2
COPD Exacerbation 1
Emphysema 1
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Condition MeSH

Condition MeSH for perforomist
Intervention Trials
Pulmonary Disease, Chronic Obstructive 5
Lung Diseases, Obstructive 4
Lung Diseases 3
Emphysema 1
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Clinical Trial Locations for perforomist

Trials by Country

Trials by Country for perforomist
Location Trials
United States 28
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Trials by US State

Trials by US State for perforomist
Location Trials
South Carolina 4
Florida 3
North Carolina 3
Missouri 3
Arizona 2
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Clinical Trial Progress for perforomist

Clinical Trial Phase

Clinical Trial Phase for perforomist
Clinical Trial Phase Trials
Phase 4 2
Phase 3 1
Phase 2 2
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Clinical Trial Status

Clinical Trial Status for perforomist
Clinical Trial Phase Trials
Completed 5
Withdrawn 1
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Clinical Trial Sponsors for perforomist

Sponsor Name

Sponsor Name for perforomist
Sponsor Trials
Mylan Inc. 2
Theravance Biopharma 2
Mylan Specialty L.P. 1
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Sponsor Type

Sponsor Type for perforomist
Sponsor Trials
Industry 8
Other 4
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