Study identifier:D3320C00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A 4-week, Double-Blind, Placebo-Controlled, Randomised, Parallel group, Multi-Centre, Phase IIa Study to Investigate the Tolerability and Safety of 100 mg Oral AZD2423 in Patients with Moderate to Severe COPD
Chronic Obstructive Pulmonary Disease
Phase 2
No
AZD2423, Placebo to AZD2423
All
63
Interventional
40 Years - 80 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Oct 2014 by AstraZeneca
AstraZeneca
-
The purpose of the study is to investigate the tolerability and safety of AZD2423 in Patients with chronic obstructive pulmonary disease.
Location
Location
Russe, Bulgaria
Location
Sofia, Bulgaria
Location
Bratislava, Slovakia
Location
Kosice, Slovakia
Location
Presov, Slovakia
Location
Zilina, Slovakia
Arms | Assigned Interventions |
---|---|
Experimental: AZD2423 AZD2423 Oral Treatment for 28 days | Drug: AZD2423 100 mg oral treatment once daily for 28 days |
Placebo Comparator: Placebo Oral treatment for 28 days | Drug: Placebo to AZD2423 Oral treatment once daily for 28 days |
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