A single-centre, single-blind, randomised, placebo-controlled, single-dose phase I study to assess the safety, tolerability and pharmacokinetics after single ascending oral and intravenous doses of AZD1305 in healthy male subjects
Study identifier:D3190C00001
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A single-centre, single-blind, randomised, placebo-controlled, single-dose phase I study to assess the safety, tolerability and pharmacokinetics after single ascending oral and intravenous doses of AZD1305 in healthy male subjects
Medical condition
Safety
Phase
Phase 1
Healthy volunteers
-
Study drug
-
Sex
-
Actual Enrollment
-
Study type
Interventional
Age
-
Date
Study Start Date: 01 Jan 2007
Primary Completion Date: -
Study Completion Date: -
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
Verified 01 Nov 2013 by AstraZeneca
Sponsors
AstraZeneca
Collaborators
-
Inclusion and exclusion criteria
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