To assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of single ascending doses of inhaled AZD8683

Study identifier:D1883C00006

ClinicalTrials.gov identifier:N/A

EudraCT identifier:2011-002412-87

CTIS identifier:N/A

Study Complete

Official Title

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

Medical condition

Healthy

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD8683, Placebo to match

Sex

Male

Actual Enrollment

38

Study type

Interventional

Age

18 Years - 45 Years

Date

Study Start Date: 01 Oct 2011
Primary Completion Date: 01 May 2012
Study Completion Date: 01 May 2012

Study design

Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Basic Science

Verification:

Verified 01 Dec 2013 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria