Study identifier:BY217/M2-110
ClinicalTrials.gov identifier:NCT00062582
EudraCT identifier:N/A
CTIS identifier:N/A
A 24 Week, Placebo-Controlled, Randomized, Parallel Group Study Comparing Roflumilast 500 mcg Daily vs Placebo on Pulmonary Function and Respiratory Symptoms in Patients with Chronic Obstructive Pulmonary Disease (COPD)
Chronic Obstructive Pulmonary Disease
Phase 3
No
Roflumilast
All
1000
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: None
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Sept 2016 by AstraZeneca
AstraZeneca
-
No locations available
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