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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
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental | Experimental | HGP0904 + HGP0608 + HGP0816, once daily |
|
| Active Comparator1 | Active Comparator | HGP0904 placebo + HGP0608 + HGP0816, once daily |
|
| Active Comparator2 | Active Comparator | HGP0904 + HGP0608 + HGP0816 placebo, once daily |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HGP0904 | Drug |
| ||
| HGP0608 |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage change from baseline in LDL-cholesterol at Week 8 | baseline and 8 weeks | |
| Change from baseline in sitDBP at Week 8 | baseline and 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage change from baseline in LDL cholesterol at Week 4 | baseline and 4 weeks | |
| Percentage change from baseline in Total cholesterol, HDL cholesterol, Triglyceride at Week 4,8 | baseline, 4weeks and 8 weeks |
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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
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| 23 institutions including Samsung Medical Center | Seoul | South Korea |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29150250 | Derived | Lee HY, Kim SY, Choi KJ, Yoo BS, Cha DH, Jung HO, Ryu DR, Choi JH, Lee KJ, Park TH, Oh JH, Kim SM, Choi JY, Kim KH, Shim J, Kim WS, Choi SW, Park DG, Song PS, Hong TJ, Rhee MY, Rha SW, Park SW. A Randomized, Multicenter, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and the Tolerability of a Triple Combination of Amlodipine/Losartan/Rosuvastatin in Patients With Comorbid Essential Hypertension and Hyperlipidemia. Clin Ther. 2017 Dec;39(12):2366-2379. doi: 10.1016/j.clinthera.2017.10.013. Epub 2017 Nov 14. |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Aug 24, 2017 | |
| Reset | Mar 19, 2018 |
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|
| HGP0816 | Drug |
|
| HGP0904 Placebo | Drug |
|
| HGP0816 Placebo | Drug |
|
| Change from baseline in sitDBP at Week 4 | baseline and 4weeks |
| Change from baseline in sitSBP at week 4, 8 | baseline, 4weeks and 8 weeks |
| Proportion of subjects achieving LDL-cholesterol goals by cardiovascular risk category at Week 4, 8 | baseline, 4weeks and 8 weeks |
| Proportion of subjects achieving Blood Pressure control by cardiovascular risk category at Week 4, 8 | baseline, 4weeks and 8 weeks |
| Proportion of subjects achieving LDL-cholesterol goals and Blood Pressure control by cardiovascular risk category at Week 4, 8 | baseline, 4weeks and 8 weeks |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Aug 24, 2017 | Mar 19, 2018 |
| ID | Term |
|---|---|
| D006973 | Hypertension |
| D006949 | Hyperlipidemias |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D050171 | Dyslipidemias |
| D052439 | Lipid Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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