Study identifier:D3550C00014
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase II Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy of 28-Day Oral Administration of AZD5069 Twice Daily in Patients with Bronchiectasis
bronchiectasis
Phase 2
No
AZD5069, Placebo
All
83
Interventional
18 Years - 80 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Sept 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
The purpose of this study is to investigate the effect of AZD5069 in patients with bronchiectasis.
Location
Location
OSTRAVA, Czech Republic
Location
PRAGUE, Czech Republic
Location
HULL, East Yorkshire, United Kingdom
Location
LEICESTER, Leicestershire, United Kingdom
Location
BIRMINGHAM, WSTMID, United Kingdom
Location
BELFAST, United Kingdom
Location
BRISTOL, United Kingdom
Location
CAMBRIDGE, United Kingdom
Arms | Assigned Interventions |
---|---|
Experimental: 1 Treatment arm AZD5069 | Drug: AZD5069 Oral dose bid |
Placebo Comparator: 2 Placebo dose. | Drug: Placebo Oral dose bid |
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