Study identifier:D1883C00006
ClinicalTrials.gov identifier:N/A
EudraCT identifier:2011-002412-87
CTIS identifier:N/A
A Phase I, Single Centre, Double-blind, Randomised, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of inhaled AZD8683 after Single Ascending Doses administered via Turbuhaler in Healthy Subjects
Healthy
Phase 1
Yes
AZD8683, Placebo to match
Male
38
Interventional
18 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Dec 2013 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Group 1 - 4, single ascending dose AZD 8683 Subjects will participate in 1 of 4 groups. In each group, 6 subjects will receive AZD8683 and 2 subjects will receive placebo. | Drug: AZD8683 Single Dose Inhaled IMP via Turbuhaler |
Placebo Comparator: Group 1-4 single ascending dose Placebo Subjects will participate in 1 of 4 groups. In each group, 6 subjects will receive AZD8683 and 2 subjects will receive placebo. | Drug: Placebo to match Single dose Inhaled Placebo via Turbuhaler |