Study identifier:LAS-MD-35
ClinicalTrials.gov identifier:NCT01044459
EudraCT identifier:N/A
CTIS identifier:N/A
A Long-Term, Randomized, Double-Blind Study of the Safety, Tolerability and Efficacy of Aclidinium Bromide At Two Dosage Levels When Administered to Patients With Moderate to Severe, Stable Chronic Obstructive Pulmonary Disease
Chronic Obstructive Pulmonary Disease
Phase 3
No
Aclidinium Bromide 200 µg, Aclidinium Bromide 400 µg
All
605
Interventional
40 Years +
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Feb 2017 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Aclidinium Bromide 200 µg aclidinium bromide, inhaled, 52 weeks of treatment | Drug: Aclidinium Bromide 200 µg aclidinium bromide 200 μg, oral inhalation twice per day for 52 weeks of treatment |
Experimental: Aclidinium Bromide 400 µg aclidinium bromide, inhaled, 52 weeks of treatment | Drug: Aclidinium Bromide 400 µg aclidinium bromide 400 μg, oral inhalation twice per day for 52 weeks of treatment |