Study to Assess the Safety and Tolerability of PT010, PT009 and PT003 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease



Status:Completed
Conditions:Chronic Obstructive Pulmonary Disease, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:40 - 80
Updated:8/31/2018
Start Date:August 10, 2015
End Date:September 12, 2017

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A Randomized, Double-Blind, Parallel-Group, 52-Week, Chronic-Dosing, Multi-Center Study to Assess the Safety and Tolerability of PT010, PT009 and PT003 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease

Study to Assess the Safety and Tolerability of PT010, PT009 and PT003 in Subjects with
Moderate to Very Severe Chronic Obstructive Pulmonary Disease

A Randomized, Double-Blind, Parallel-Group, 52-Week, Chronic-Dosing, Multi-Center Study to
Assess the Safety and Tolerability of PT010, PT009 and PT003 in Subjects with Moderate to
Very Severe Chronic Obstructive Pulmonary Disease

Inclusion Criteria:

Given their signed written informed consent to participate. Must have agreed to participate
in and complete the lead-in Study PT010006.(NCT02497001)

Exclusion Criteria:

Severe osteoporosis Unable to achieve an acceptable DEXA scan Inability to achieve pupil
dilation to at least 6 mm Subjects with an implanted artificial intraocular lens or are
scheduled to undergo cataract surgery
We found this trial at
61
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Columbus, Georgia
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Abingdon, Virginia
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Rincon, Georgia 31326
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