Evaluate the Efficacy and Safety of SPC1001 and Monotherapy in Patients With Essential Hypertension

NCT ID: NCT06212648

Last Updated: 2024-01-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

253 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-25

Study Completion Date

2023-01-27

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study purpose is to determine the appropriate combination drug dose by comparing safety and efficacy with placebo, candesartan, and amlodipine monotherapy after 8 weeks of administration of SPC1001 to patients with essential hypertension.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This clinical trial is a randomized, double-blind, parallel design, placebo and active drug comparison, and multicenter clinical trial to evaluate the safety and efficacy of investigational drugs after 8 weeks of administration.

Subjects who meet the selection and exclusion criteria should take a placebo for 2 weeks during the run-in period and run a lifestyle improvement program in parallel.

However, if you are already taking antihypertensive drugs at the time of screening, you should stop taking your existing antihypertensive drugs for at least 4 weeks from before the run-in period to the time of randomization to avoid affecting the clinical trial results.

Subjects who meet the final selection and exclusion criteria at the end of the run-in period are randomly assigned 1:1:1:1:1:1:1:1 to each administration group, receive a prescription for clinical trial drugs, and administer for 8 weeks in a double-blind manner.

Encourage the subjects to continuously perform the lifestyle improvement program for 8 weeks during the administration of the clinical investigational drug and visit the testing institution at 4 and 8 weeks during the 8-week trial period, excluding randomized visits, to check the efficacy and safety.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hypertension Essential Hypertension

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This clinical trial is a randomized, double-blind, parallel design, placebo and active drug comparison, and multicenter clinical trial to evaluate the safety and efficacy of investigational drugs after 8 weeks of administration.
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators
double blind

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

SPC1001 High

SPC1001 High (Candesartan/Amlodipine/Indapamide)

Group Type EXPERIMENTAL

SPC1001 High

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

SPC1001 Mid1

SPC1001 Mid1 (Candesartan/Amlodipine/Indapamide)

Group Type EXPERIMENTAL

SPC1001 Mid1

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

SPC1001 Mid2

SPC1001 Mid1 (Candesartan/Amlodipine/Indapamide)

Group Type EXPERIMENTAL

SPC1001 Mid2

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

SPC1001 Low

SPC1001 Low (Candesartan/Amlodipine/Indapamide)

Group Type EXPERIMENTAL

SPC1001 Low

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

SPC3001

SPC3001 (Candesartan 8mg)

Group Type ACTIVE_COMPARATOR

SPC3001

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

SPC4001

SPC4001 (Amlodipine 5mg)

Group Type ACTIVE_COMPARATOR

SPC4001

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

SPC4002

SPC4002 (Amlodipine 10mg)

Group Type ACTIVE_COMPARATOR

SPC4002

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Placebo

SPC1001(High, Mid1, Mid2, Low) placebo, SPC3001 placebo, SPC4001 placebo, SPC4002 placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

SPC1001 High

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

SPC1001 Mid1

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

SPC1001 Mid2

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

SPC1001 Low

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

SPC3001

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

SPC4001

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

SPC4002

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

Placebo

Drugs for clinical trials are orally administered once a day after breakfast.

After randomization, the drug for clinical trials is taken once a day (total of 4 tablets) for 8 weeks.

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Candesartan 8mg Amlodipine 5mg Amlodipine 10mg

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Men and women between the ages of 19 and 75
2. Those whose blood pressure measured at the time of screening meets the following criteria 2.1 Not taking antihypertensive drugs (Naïve): 140 mmHg ≤ MSSBP (mean sitting SBP) \< 180 mmHg 2.2 If you are taking antihypertensive drugs or have diabetes or chronic kidney disease: 130 mmHg ≤ MSSBP \< 180 mmHg
3. Those whose blood pressure measured at the time of randomization meets the following criteria 3.1. 140 mmHg ≤ MSSBP \< 180 mmHg 3.2. Or patients with diabetes or chronic kidney disease 130 mmHg ≤ MSSBP \< 180 mmHg (However, patients with chronic kidney disease who have clinically significant albuminuria or proteinuria within 6 months)
4. Those who voluntarily agreed to participate in this clinical trial and signed the consent form

Exclusion Criteria

1. Those whose blood pressure measured at screening and randomization is MSDBP (Mean Sitting DBP) ≥ 110 mmHg
2. Patients who showed a difference of SBP 20 mmHg or more and DBP 10 mmHg or more in blood pressure measured 3 times in both arms at screening
3. Patients with a history of secondary hypertension or any history of suspected secondary hypertension (aortic stenosis, primary hyperaldosteronemia, renal artery stenosis, Cushing's disease, pheochromocytoma, polycystic kidney disease, etc.)
4. Patients with symptomatic orthostatic hypotension
5. Patients requiring concomitant administration of other antihypertensive drugs in addition to investigational drugs during clinical trial participation (Diuretics, β-blockers, ACE inhibitors, Angiotensin II Receptor Blocker, Calcium Channel Blockers, α-blockers, Renin Inhibitors, Vasodilators, etc.)
6. Patients with the following past medical history/comorbidities at the screening visit 6.1. Uncontrolled diabetic patients with HbA1c ≥ 9% 6.2. Patients with severe heart disease (heart failure (NYHA class 3 and 4)), ischemic heart disease (unstable angina, acute myocardial infarction) within 6 months of screening, peripheral vascular disease, percutaneous coronary angioplasty or coronary artery bypass surgery ruler) 6.3. Patients with clinically significant ventricular tachycardia, atrial fibrillation, atrial flutter, or other arrhythmias determined by the investigator to be clinically significant 6.4. Patients with hypertrophic obstructive cardiomyopathy, severe obstructive coronary artery disease, hemodynamically significant aortic stenosis, stenosis on the aortic or mitral valve 6.5. Patients with the severe cerebrovascular disorder (stroke, cerebral infarction, cerebral hemorrhage, etc. within 6 months of screening) 6.6. Patients with known moderate or malignant retinopathy (retinal hemorrhage within 6 months of screening, visual impairment, retinal microaneurysm) 6.7. Patients with wasting disease, autoimmune disease, connective tissue disease 6.8. Patients with gastrointestinal diseases and surgeries that may affect drug absorption, distribution, metabolism, and excretion, current active gastritis, gastrointestinal/rectal bleeding, gastric ulcer, pancreatic dysfunction such as pancreatitis, active inflammatory bowel syndrome within 12 months of screening Back (However, simple appendectomy and hernia surgery are excluded) 6.9. Patients with hereditary angioedema or with a history of angioedema when treated with ACE inhibitors, renin inhibitors, or angiotensin II receptor antagonists 6.10. cholestatic disease patient 6.11. shock patient 6.12. Patients with anuria 6.13. Patients with symptomatic hyperuricemia (history of gout or uric acid stones) 6.14. Patients with a history of malignant tumors including leukemia and lymphoma within 5 years of screening (however, those who have been evaluated as having complete response after treatment and have not relapsed within 2 years of screening, or malignant tumors that have occurred are the only Those with basal cell carcinoma or squamous cell carcinoma of the skin can participate in this test) 6.15. Patients with any chronic inflammatory condition requiring chronic anti-inflammatory treatment
7. Persons whose laboratory test results at the screening visit fall under the following 7.1. Those whose ALT or AST levels are more than 3 times the upper limit of normal organ 7.2. Those whose serum creatinine level is 1.5 times or more of the upper limit of normal organ 7.3. Patients with renal impairment with severe renal failure with Creatinine Clearance (CrCl) \< 30 mL/min or eGFR \< 30 ml/min/1.73 m2 7.4. Hypokalemia (Serum K \< 3.5 mmol/L) 7.5. Persons with hyperkalemia (Serum K \> 5.5 mmol/L) 7.6. Those with hyponatremia (Serum Na \< 135.0 mmol/L) 7.7. Those with hypercalcemia (Serum Ca \> 2.75 mmol/L or 11 mg/dL)
8. Those with genetic problems such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption
9. Persons with or suspected of drug or alcohol abuse
10. Pregnant or lactating women
11. Women and men of childbearing potential who do not agree to use a combination of effective or medically acceptable contraceptive methods\* for the duration of the clinical trial and 4 weeks after administration of the last investigational drug

\* Taking birth control pills or implanting hormones, implanting intrauterine devices or intrauterine systems, double-blocking methods (both male (condom) and female (contraceptive diaphragm, vaginal sponge or cervical cap) using a contraceptive device), sterilization ( vasectomy, tubal ligation, etc.)
12. Persons with a history of hypersensitivity to clinical investigational drug components and other dihydropyridine drugs, thiazide drugs, or sulfonamide derivatives
13. Those who participated in another clinical trial within 4 weeks before the screening visit and received the investigational drug
14. Others who are judged to be unable to participate in clinical trials cording to the judgment of the investigator
Minimum Eligible Age

19 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Shin Poong Pharmaceutical Co. Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

CHA Gangnam Medical Center, CHA University

Seoul, Gangnam, South Korea

Site Status

Countries

Review the countries where the study has at least one active or historical site.

South Korea

References

Explore related publications, articles, or registry entries linked to this study.

Shin J, Kim S, Han K, Kim M, Ahn Y, Sohn I, Kim K, Cha D, Hong S, Cho E, Lee H, Pyun W, Youn H, Kim W, Rhee M, Lee J, Ha J, Choi J, Yoo B, Jeong J, Chung W, Jeong Y, Kim C. Multicenter, Randomized, Double-Blind, Parallel, Phase 2 Clinical Trial to Compare and Evaluate the Efficacy and Safety of SPC1001 and Monotherapy in Patients With Essential Hypertension. Clin Ther. 2025 Oct 28:S0149-2918(25)00347-9. doi: 10.1016/j.clinthera.2025.10.001. Online ahead of print.

Reference Type DERIVED
PMID: 41162308 (View on PubMed)

Related Links

Access external resources that provide additional context or updates about the study.

https://www.semanticscholar.org/paper/From-epidemiological-transition-to-modern-in-the-Blacher-L%C3%A9vy/30ae7ff48d49b03b7ba4a4c4533e52d187ab0dc3

From epidemiological transition to modern cardiovascular epidemiology: hypertension in the 21st century

https://journals.lww.com/jhypertension/Abstract/2009/05000/When_should_antihypertensive_drug_treatment_be.3.aspx

When should antihypertensive drug treatment be initiated and to what levels should systolic blood pressure be lowered? A critical reappraisal

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

SP-CAP-002

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.