A 28-Day Parallel Group Study of TD-4208 in COPD



Status:Completed
Conditions:Chronic Obstructive Pulmonary Disease, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:40 - Any
Updated:5/5/2014
Start Date:March 2014
End Date:October 2014
Contact:Andrew Nicholls, MD
Email:Anicholls@theravance.com
Phone:650-808-6400

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A Phase IIB, 28-Day, Randomized, Double-Blind Placebo-Controlled Parallel Group Study of Nebulized TD-4208 in Subjects With Chronic Obstructive Pulmonary Disease

This study will evaluate the safety and efficacy of four doses of TD-4208 and a placebo
product when administered once daily for 28 days using a jet nebulizer to patients with
moderate to severe chronic obstructive pulmonary disease.


Inclusion Criteria:

- Subject is a male or female subject 40 years of age or older

- Subject must have a negative pregnancy test, and must be prepared to use effective
contraception if of child-bearing potential

- Subject is capable of performing reproducible spirometry maneuvers

- Subject has post-bronchodilator FEV1/FVC ratio <0.7

- Subject has moderate-to-severe stable COPD (Stage 2 or 3 according to the GOLD
Guidelines)

- Subject has a post-bronchodilator FEV1 greater than or equal to 30% and less than 80%
of predicted normal

- Subject has a current or past smoking history of at least 10 pack-years.

Exclusion Criteria:

- Subject has a significant respiratory disease or disorder other than COPD that would
affect the interpretation of data from this study

- Subject has a history of reactions or hypersensitivity to inhaled or nebulized
anticholinergic or beta-agonist agents

- Subject suffers from any medical condition that would preclude the use of inhaled
anticholinergic agents

- Subject has been hospitalized for COPD or pneumonia within 12 weeks

- Subject requires long-term oxygen therapy (>15 hours a day)
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