To examine variation rate of Non-HDL with KI1107 comparison Rosuvastatin monotherapy.
Drug: KI1107 4 Capsules, QD
Drug: Rosuvastatin Calcium 20 MG, QD
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Full eligibility criteria for NCT03026933
Ages eligible for Study
19 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
High risk for cardiovascular disease according to NCEP APT III
TG≥130mg/dL and 160mg/dL>LDL-C≥100mg/dL for subjects who were not taking statins for 4 weeks
500mg/dL>TG≥200mg/dL and LDL-C<110mg/dL for subjects who were taking statins for 4 weeks
Reduction of LDL-C dompairng screening visit
The patient has histories of acute artery disease within 3 months
The patient has histories of operation revasculatiation or aneurysm within 6 months
The patient has histories of Unexplained myaliga or diagnosed myalgia or rhabdomyolysis
The patient has histories of Effectable disease to the procedrue and clinical trial result
All locations for NCT03026933
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Tris trial is registered with FDA with number: NCT03026933. The sponsor of the trial is Kuhnil Pharmaceutical Co., Ltd. and it is looking for 215 volunteers for the current phase.
Official trial title: A Multi-center, Randomized, Double Blind, Parallel Phase III Study to Evaluate the Efficacy and Safety of KI1107 in Patients Whose TG Level is Not Adequately Controlled With Rosuvastatin Calcium Monotherapy While LDL-C is Properly Controlled
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