Study identifier:4522IL/0015
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An Open, Non-Randomised, Parallel-Group, Non-Controlled, Phase I Trial to Assess the Effect of Age and Gender on the Pharmacokinetics of a Single 40 mg Oral Dose of ZD4522 in Healthy Male and Female Volunteers
hypercholesterolaemia
N/A
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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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