Study identifier:D5200C00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I Study in Healthy Volunteers to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD4721 after Once Daily Administration of Multiple Ascending Doses for 10 days, and an Open-label Comparison with the Pharmacodynamics of AZD5069 given Twice Daily for 3 days
Chronic obstructive pulmonary disease (COPD).
Phase 1
Yes
AZD4721, Placebo, AZD5069
All
84
Interventional
18 Years - 50 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Basic Science
Verified 01 Jun 2015 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Part A AZD4721 Part A of the study, multiple ascending doses of AZD4721 will be administrated once daily for 10 days | Drug: AZD4721 Part A - multiple ascending dose, daily; Part B - one dose decided after part A, daily |
Placebo Comparator: Placebo Part A of the study, multiple ascending doses of matching Placebo will be administrated once a daily for 14 days | Drug: Placebo Part A - multiple ascending dose daily |
Active Comparator: AZD5069, then AZD4721 Part B of the study, subject will participate in two treatment periods (one with AZD5069 administrated for 3 days and the second period with AZD4721 administrated for 14 days) separated by a wash-out period of 6-10 days between the two periods. | Drug: AZD4721 Part A - multiple ascending dose, daily; Part B - one dose decided after part A, daily Drug: AZD5069 Part B - one dose decided after part A, twice a day |