Efficacy and Safety of Co-administered HGP0904, HGP0608 and HGP0816 in Patients With Hypertension and Dyslipidemia: A Randomized, Double-blind, Multicenter, Phase 3 Study
Efficacy and Safety of Co-administered HGP0904, HGP0608 and HGP0816 in Patients With Hypertension and Dyslipidemia: A Randomized, Double-blind, Multicenter, Phase 3 Study
A phase 3 study to evaluate efficacy and safety 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:
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