Study identifier:D0520C00004
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised, double blind, placebo controlled, parallell group, phase 1 study to assess the safety, tolerability and pharmacokinetics of single and mutlitple ascending oral doses of AZD9668 in healthy japanese and caucasion volunteers
pharmacokinetics
Phase 1
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Interventional
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Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
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No locations available
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