Study identifier:D4350C00005
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A 4-Week Dose-Ranging Study to Evaluate Antidyslipidemic Effects, Other Pharmacodynamic Effects, Safety, and Tolerability of AZD6610 with Concomitant Open-Label Simvastatin Therapy in Patients with Elevated Triglycerides, Elevated Low Density Lipid Cholesterol and Abdominal Obesity: a Randomized, Double-Blind, Placebo-Controlled, Multi-Centre, Parallel-Group Study with Fenofibrate as Reference
hypercholesterolaemia
Phase 2
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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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