Study identifier:D3560L00053
ClinicalTrials.gov identifier:NCT00335699
EudraCT identifier:N/A
CTIS identifier:N/A
A 6-week, randomised, open-label, parallel group, multi-centre study to compare the efficacy of rosuvastatin 10mg with atorvastatin 10mg in the treatment of non-diabetic metabolic syndrome subjects with raised LDL-C
Hypercholesterolemia
Phase 4
No
Rosuvastatin
All
370
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Jun 2025 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The primary objective of this study is to compare the effect of rosuvastatin 10mg with atorvastatin 10mg in the percentage reduction of LDL-C in Subjects with metabolic syndrome after 6 weeks of treatment.
Location
Location
Pusan, Republic of Korea
Location
DaeGu, Republic of Korea
Location
JinJu, Republic of Korea
Location
Ulsan, Republic of Korea
Location
KwangJu, Republic of Korea
Location
JeonJu, Republic of Korea
Location
IkSan, Republic of Korea
Arms | Assigned Interventions |
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