Clinical Efficacy and Safety Evaluation of Co-administered HGP0904, HGP0608 and HGP0816 in Patients With Hypertension and Dyslipidemia

This study is designed as a multi-center, double-blinded, randomized, phase 3 clinical trial to evaluate the efficacy and safety of Co-administered HGP0904, HGP0608 and HGP0816 in Patients with Hypertension and Dyslipidemia

Inclusion criteria

• 19 ≤ age ≤ 75
• at Visit 1 1) BP: sitDBP ≥ 90mmHg 2) Cholesterol : LDL-C ≤ 250mg/dL, TG < 400mg/dL
• at Visit 2 : after TLC (after 4weeks) 1) BP: 80 mmHg ≤ sitDBP < 110mmHg 2) Cholesterol : following risk category (Cardiovascular Risk category) A : CHD risk factor 0 - 1, 160mg/dL ≤ LDL-C ≤ 250mg/dL B①: CHD risk factor≥2 and 10 year risk <10%, 160mg/dL ≤ LDL-C ≤ 250mg/dL B②: CHD risk factor≥2 and 10 year risk =10-20%, 130mg/dL ≤ LDL-C ≤ 250mg/dL C : CHD/CHD risk equivalents* or 10 year risk>20 ,100mg/dL ≤ LDL-C ≤ 250mg/dL 3) TG < 400mg/dL 4. Patients understood the contents and purpose of this trial and signed informed consent form

Exclusion criteria

• At Visit 1, BP difference SBP ≥20mmHg or DBP ≥10mmHg
• Tolerance or Hypersensitivity Angiotensin II receptor blocker or HMG-CoA. reductase inhibitor, Calcium channel blocker(dihydropyridine) or Multi-drug allergy
• Fibromyalgia, myopathy, rhabdomyolysis or acute myopathy or medical history of adverse effect to statin
• CPK normal range ≥ 3times
• Uncontrolled primary hypothyroidism(TSH normal range ≥ 2 times)
• Renal disease or suspected renal disease (Scr ≥ 2mg/dL, AST or ALT≥2 times)
• Active gout or hyperuricemia(at Visit 1, uric acid > 9mg/dL)
• IDDM or uncontrolled diabetes mellitus (HbA1c>9%)
• ventricular arrhythmia
• medical history

• severe cerebrovascular disease within 6 months (cerebral infarction, cerebral hemorrhage), hypertension
• encephalopathy, transient cerebral ischemic attack(TIA)
• severe heart disease(heart failure of NYHA class III-IV), valvular disease of heart or myocardial infarction and unstable angina
• angioplasty or coronary artery bypass graft(CABG) surgery within 6months