Expired Study
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Stockbridge, Georgia


The primary objective of this study is to demonstrate efficacy of PT003 MDI relative to its individual components (PT001 MDI and PT005 MDI) in patients with moderate to severe chronic obstructive pulmonary disease (COPD).


Key Inclusion Criteria: - Signed written informed consent - 40 - 80 years of age - Clinical history of COPD with airflow limitation that is not fully reversible - Females of non-child bearing potential or females of child bearing potential with negative pregnancy test; and acceptable contraceptive methods - Current/former smokers with at least a 10 pack-year history of cigarette smoking - A measured post- bronchodilator FEV1/FVC ratio of < or = 0.70 - A measured post- bronchodilator FEV1 > or = 750ml or 30% predicted and < or = 80% of predicted normal values - Able to change COPD treatment as required by protocol Key Exclusion Criteria: - Women who are pregnant or lactating - Primary diagnosis of asthma - Alpha-1 antitrypsin deficiency as the cause of COPD - Active pulmonary diseases - Prior lung volume reduction surgery - Abnormal chest X-ray (or CT scan) not due to the presence of COPD - Hospitalized due to poorly controlled COPD within 3 months of Screening - Clinically significant medical conditions that preclude participation in the study (e.g. clinically significant abnormal ECG, uncontrolled hypertension, glaucoma, symptomatic prostatic hypertrophy) - Cancer that has not been in complete remission for at least 5 years - Treatment with investigational study drug or participation in another clinical trial or study within the last 30 days or 5 half lives Other inclusion/exclusion criteria as defined in the protocol



Primary Contact:

Study Director
Colin Reisner, M.D.
Pearl Therapeutics, Inc.

Backup Contact:


Location Contact:

Stockbridge, Georgia
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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