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CompletedNCT03847506REVERT-KUpdated May 10, 2022

Evaluate Efficacy and Safety of Ezetimibe/Rosuvastatin and Candesartan Cilexetil/Amlodipine Besylate Combination Tablets

A Phase 4 interventional study of Ezetimibe/Rosuvastatin and Candesartan cilexetil/Amlodipine besylate in Hypertension, Hyperlipidemia, sponsored by HK inno.N Corporation. Completed at 1 site in Korea, Republic of. Open to participants aged 19 Years to 74 Years. Per ClinicalTrials.gov, last updated 2022-05-10.

Sponsored by HK inno.N Corporation · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jul 2018, registered Nov 2018).
Phase
Phase 4
Study type
Interventional
Enrollment
127
Allocation
Randomized
Ages
19 Years to 74 Years
Sex
All
01

Study summary

To evaluate the efficacy and the safety of concomitant use of Ezetimibe/Rosuvastatin combination tablets and Candesartan cilexetil/Amlodipine besylate combination tablets compared to each combination tablet alone in patients with essential hypertension (HTN) and hyperlipidemia.

Read the detailed description

To improve the ease of use of high blood pressure and hyperlipidemia to improve patient compliance and reduce the risk of cardiovascular disease.

And It is recommended to identify the need to develop a combination of Candesartan cilexetil/Amlodipine besylate combination tablets , and Ezetimibe/Rosuvastatin combination tablets.

02

Conditions studied

  • Hypertension, Hyperlipidemia

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03

In context

Hyperlipidemias

821 studies on the registry are indexed under Hyperlipidemias; 105 are open to participants now.

This study's enrollment of 127 is above the median of 87 across 691 interventional studies indexed under Hyperlipidemias.

Browse Hyperlipidemias studies →

Lead sponsor

HK inno.N Corporation is the lead sponsor of 99 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 74 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

[ Inclusion Criteria ]

  1. Adults aged 19 to \<75 years.
  2. Diagnosed with essential HTN accompanied by hyperlipidemia (average siSBP ≥140 mmHg and LDL-C ≥100 mg/dL) or being treated for the condition after the diagnosis, at Visit 1 (screening).
  3. Provided the signed informed consent form voluntarily after receiving explanation of the objectives, methods and effects of the study.
  4. Medically sterile or agreed to use medically acceptable contraceptive method during the study.

[ Exclusion Criteria ]

* Criteria Related to HTN and Dyslipidemia

  1. Severe HTN defined as average siDBP ≥110 mmHg or average siSBP ≥180 mmHg at Visit 1 (screening).
  2. The difference in BPs between those measured at both arms at Visit 1 (screening) is ≥10 mmHg for siDBP or ≥20 mmHg for siSBP.
  3. LDL-C >250 mg/dL or TG ≥400 mg/dL at Visit 1 (screening).
  4. Diagnosed with or suspected of secondary HTN (e.g., renovascular disease, coarctation of the aorta, hyperaldosteronism, unilateral or bilateral renal artery stenosis, Cushing's syndrome, pheochromo-cytoma, polycystic kidney disease, etc.).

  5. Patients with symptomatic orthostatic HTN (difference in BPs between the value measured in supine position and the value measured in standing position is ≥20 mmHg for siSBP or ≥10 mmHg for siDBP).

    * Criteria Related to Medical History

  6. Diagnosis with type 1 diabetes mellitus (DM) or uncontrolled DM (patients on insulin therapy or patients with HbA1C ≥9%).
  7. Patients with severe heart disease - heart failure (NYHA Classes 3 and 4), history of ischemic cardiac disease (unstable angina, myocardial infarction), peripheral vascular diseases, percutaneous transluminal angioplasty, or coronary artery bypass graft within the recent 3 months.
  8. Patients with clinically significant ventricular tachycardia, atrial fibrillation, atrial flutter, or other clinically significant arrhythmia at the discretion of the investigator.
  9. History of muscular toxicity while on treatment with other HMG-CoA reductase inhibitors or fibrates.
  10. History of angioedema while on treatment with ACE inhibitors or ARBs.
  11. History of hypersensitivity to ARBs, dihydropyridines, or HMG-CoA reductase inhibitors.
  12. Patients with hypertrophic occlusive myocardiopathy, severe occlusive coronary artery disease, aortic stenosis, hemodynamically significant aortic, or mitral valve stenosis.
  13. Presence of severe cerebrovascular disorders (diagnosis of stroke, cerebral infarction, or cerebral hemorrhage within the recent 6 months).
  14. History or current evidence of wasting diseases, autoimmune diseases (such as rheumatoid arthritis and systemic lupus erythematosus), or connective tissue diseases.
  15. Known diagnosis of moderate or malignant retinopathy (including retinal hemorrhage, visual disturbance, and retinal microaneurysm within the recent 6 months).
  16. Patients with surgical or medical gastrointestinal diseases or having received surgery that could interfere with drug absorption, distribution, metabolism, and elimination and patients with active gastritis, gastrointestinal/rectal bleeding, or diagnosed with active inflammatory bowel disease within the recent 12 months.
  17. History of malignancy including leukemia and lymphoma within the recent 5 years (except for localized basal cell carcinoma of the skin).
  18. Patients with any inflammatory diseases requiring chronic anti-inflammatory therapy.
  19. Patients who received kidney transplant or with only one kidney.
  20. Presence of biliary obstruction or cholestasis.
  21. Presence of hereditary conditions such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption.

  22. Patients with shock.

    * Criteria Related to Clinical Laboratory Tests

  23. Laboratory abnormalities as follows:

    • AST or ALT >3 x upper limit of normal (ULN);
    • Serum creatinine >1.5 x ULN.
  24. History of myopathy or rhabdomyolysis (e.g., serum CK ≥5 x ULN).
  25. Uncontrolled abnormal thyroid function (e.g., TSH ≥1.5 x ULN).
  26. Persistent abnormal serum potassium level (e.g., serum potassium level \<3.5 mmol/L or >5.5 mmol/L).

  27. Patients with conditions of body fluid depletion or laboratory findings indicating clinically significant electrolyte abnormality.

    * Others

  28. Needs for concomitant administration of non-study antihypertensive agents or prohibited medications during the study.
  29. Pregnant or lactating women.
  30. History of drug or alcohol abuse within the recent 1 year.
  31. Having received other investigational product within 4 weeks prior to screening.
  32. Patients considered ineligible for the study at the discretion of the principal investigator (PI) or study staff.
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
127 participants (actual)

Study arms

  • Experimental
    EZE/ROS+CAN/AML

    Ezetimibe/Rosuvastatin 10 mg/10 mg and Candesartan cilexetil/Amlodipine besylate 8 mg/5 mg, once a day for 6 weeks

    Drug: Ezetimibe/Rosuvastatin

  • Active comparator
    CAN/AML

    Candesartan cilexetil/Amlodipine besylate 8 mg/5 mg, once a day for 6 weeks

    Drug: Candesartan cilexetil/Amlodipine besylate

  • Active comparator
    EZE/ROS+CAN

    Ezetimibe/Rosuvastatin 10 mg/10 mg + Candesartan cilexetil 8 mg, once a day for 6 weeks

    Drug: Candesartan cilexetil

Interventions

  • DrugEzetimibe/Rosuvastatin

    Ezetimibe/Rosuvastatin 10 mg/10 mg + Candesartan cilexetil/Amlodipine besylate 8 mg/5 mg + Candesartan cilexetil 8 mg placebo

    Also known as: Ezetimibe/Rosuvastatin 10 mg/10 mg

  • DrugCandesartan cilexetil/Amlodipine besylate

    Candesartan cilexetil/Amlodipine besylate 8 mg/5 mg + Ezetimibe/Rosuvastatin 10 mg/10 mg placebo + Candesartan cilexetil 8 mg placebo

    Also known as: Candesartan cilexetil/Amlodipine besylate 8 mg/5 mg

  • DrugCandesartan cilexetil

    Ezetimibe/Rosuvastatin 10 mg/10 mg + Candesartan cilexetil 8 mg + Candesartan cilexetil/Amlodipine besylate 8 mg/5 mg placebo

    Also known as: Candesartan cilexetil 8 mg

06

What researchers measure

Primary outcomes

  1. Change in sitting Systolic Blood Pressure(siSBP) from baseline after 6 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. EZE/ROS + CAN arm Change in siSBP from baseline after 6 weeks of study treatment For the siSBP at baseline and after 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean change in baseline-adjusted siSBP from baseline after 6 weeks of study treatment and its standard error will be provided by treatment arm. Inter-arm comparison will be conducted using the analysis of covariance (ANCOVA) with change in siSBP as response variable and baseline siSBP and treatment arm as independent variables.

    Time frame: week 6

  2. Percentage change in LDL-C levels from baseline after 6 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. CAN/AML arm Percentage change in LDL-C levels from baseline after 6 weeks of study treatment For the percentage change in LDL-C levels at baseline and after 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean percentage change in baseline-adjusted LDL-C levels from baseline after 6 weeks of study treatment and its standard error will be provided by treatment arm. Inter-arm comparison will be conducted using the ANCOVA with percentage change in LDL-C levels as response variable and baseline LDL-C level and treatment arm as independent variables.

    Time frame: week 6

Secondary outcomes

  1. Change in siSBP from baseline after 3 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. EZE/ROS + CAN arm For the siSBP at baseline and after 3 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean change in baseline-adjusted siSBP from baseline after 3 weeks of study treatment and its standard error will be provided by treatment arm. Inter-arm comparison will be conducted using the ANCOVA with change in siSBP as response variable and baseline siSBP and treatment arm as independent variables.

    Time frame: week 3

  2. Percentage changes in LDL-C levels from baseline after 3 and 6 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. EZE/ROS + CAN arm For the LDL-C levels at baseline and after 3 and 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean percentage changes in baseline-adjusted LDL-C levels from baseline after 3 and 6 weeks of study treatment and their standard error will be provided by treatment arm. Inter-arm comparisons of the percentage changes in LDL-C levels at Week 3 and Week 6 will be conducted using the ANCOVA with percentage change in LDL-C levels as response variable and baseline LDL-C level and treatment arm as independent variables.

    Time frame: week 3 and week 6

  3. Percentage change in LDL-C levels from baseline after 3 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. CAN/AML arm For the percentage change in LDL-C levels at baseline and after 3 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean percentage change in baseline-adjusted LDL-C levels from baseline after 3 weeks of study treatment and its standard error will be provided by treatment arm. Inter-arm comparison will be conducted using the ANCOVA with percentage change in LDL-C levels as response variable and baseline LDL-C level and treatment arm as independent variables.

    Time frame: week 3

  4. Changes in siSBPs from baseline after 3 and 6 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. CAN/AML arm For the siSBP at baseline and after 3 and 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean change in baseline-adjusted siSBP from baseline after 3 and 6 weeks of study treatment and its standard error will be provided by treatment arm. Inter-arm comparison will be conducted using the ANCOVA with change in siSBP as response variable and baseline siSBP and treatment arm as independent variables.

    Time frame: week 3 and week 6

  5. Percentage changes in LDL-C/HDL-C and TC/HDL-C from baseline after 3 and 6 weeks of study treatment

    EZE/ROS + CAN/AML arm vs. CAN/AML arm For the LDL-C/HDL-C and TC/HDL-C at baseline and for their percentage changes after 3 and 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum were presented by treatment arm. The LS-mean percentage changes in baseline-adjusted LDL-C/HDL-C and TC/HDL-C levels from baseline after 3 and 6 weeks of study treatment and their standard errors will be provided by treatment arm. Inter-arm comparison will be conducted using the ANCOVA with percentage changes in LDL-C/HDL-C and TC/HDL-C levels as response variables and baseline LDL-C/HDL-C and TC/HDL-C levels and treatment arm as independent variables.

    Time frame: week 3 and week 6

  6. Changes in siDBPs from baseline after 3 and 6 weeks of study treatment

    Co-Endpoints For the siDBP at baseline and after 3 and 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean change in baseline-adjusted siDBP from baseline after 3 and 6 weeks of study treatment and its standard error will be provided by treatment arm. Inter-arm comparison will be conducted using the ANCOVA with change in siDBP as response variable and baseline siDBP and treatment arm as independent variables.

    Time frame: week 3 and week 6

  7. Proportions of subjects who achieve the treatment goal based on JNC VIII Guideline from baseline after 3 and 6 weeks of study treatment

    Co-Endpoints (HTN treatment goal: \<140/90 mmHg \[or \<150/90 mmHg for patients aged ≥60 years\]) The frequencies and proportions of subjects who achieve the treatment goal based on JNC VIII Guideline from baseline after 3 and 6 weeks of study treatment will be provided by treatment arm. The differences in the proportions of subjects who achieve the treatment goal after 3 and 6 weeks of study treatment between treatment arms will be analyzed using the Pearson's chi-square test or the Fisher's exact test.

    Time frame: week 3 and week 6

  8. Proportions of subjects who achieve the treatment goal based on NCEP ATP III Guideline from baseline after 3 and 6 weeks of study treatment

    Co-Endpoints (LDL-C treatment goal - Group I: \<160 mg/dL; Group II: \<130 mg/dL; and Group III: \<100 mg/dL) The frequencies and proportions of subjects who achieve the treatment goal based on NCEP ATP III Guideline from baseline after 3 and 6 weeks of study treatment will be provided by treatment arm. The differences in the proportions of subjects who achieve the treatment goal after 3 and 6 weeks of study treatment between treatment arms will be analyzed using the Pearson's chi-square test or the Fisher's exact test.

    Time frame: week 3 and week 6

  9. Percentage changes in TC, TG, HDL-C, apolipoprotein B, and CRP levels from baseline after 3 and 6 weeks of study treatment

    Co-Endpoints For the TC, TG, HDL-C, apolipoprotein B, and CRP levels at baseline and after 3 and 6 weeks of study treatment, the mean, standard deviation, median, minimum, and maximum will be provided by treatment arm. The LS-mean percentage changes in baseline-adjusted TC, TG, HDL-C, apolipoprotein B, and CRP levels from baseline after 3 and 6 weeks of study treatment and their standard error will be provided by treatment arm. Inter-arm comparisons of the percentage changes at Week 3 and Week 6 will be conducted using the ANCOVA with each percentage change in TC, TG, HDL-C, apolipoprotein B, and CRP levels as response variable and relevant baseline level and treatment arm as independent variables.

    Time frame: week 3 and week 6

Other outcomes

  1. Adverse events

    The safety will be evaluated for all subjects who receive at least on dose of investigational product. The number of subjects who report AEs, adverse drug reactions (ADRs), serious adverse events (SAEs), two-sided 95% CIs, incidence rate, and number of events will be provided by treatment arm. The difference between treatment arms will be analyzed using the χ2 test or Fisher's exact test. The incidences and percentages of events by severity, causality, actions taken, and outcome will be provided by treatment arm. All AEs will be coded per SOC and PT using the MedDRA; for each coded AE, the number of subjects, incidence rate, and number of events will be provided by treatment arm. In addition, for coded AEs, the number of subjects, incidence rate, and number of events by severity, causality, actions taken, and outcome will be provided by treatment arm

    Time frame: Baseline, week 3 and week 6

07

Study locations

1 site
  • Bundang Seoul National University Hospital
    Gyeonggi-do, Seongnam-si, Bundang-gu 13620, Korea, Republic of
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 10, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03847506
Lead sponsor
HK inno.N Corporation
Responsible party
Sponsor
First posted
Feb 20, 2019
Start date
Jul 5, 2018
Primary completion
Dec 2, 2020
Completion
Dec 2, 2020
Last update
May 10, 2022

Study contacts

In-Ho Chae, Ph.D
principal investigator · Bundang Seoul National University Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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