Coronary Artery DiseasePhase 4NCT05910476
Comparative Study of Rosuvastatin/Ezetimib 20/10 mg and Atovastatin/Ezetimib 40/10 mg (TOLERANT Trial)
A Phase 4 study testing a high dose of statin/ezetimib in people with Coronary Artery Disease and Dyslipidemias, run by Yonsei University at 1 site in South Korea.
Trial summary
the investigators would like to compare the differences between roschvastin and atovastatin in patients who require high-dose statin/ejetimib to undergo a new generation of drug elution stent implantation for cardiovascular disease and maintain LDL cholesterol below 55 mg/dL. Read more about this study
- Who is it for?
- Ages 19 years and older
- Conditions the study is for
- Coronary Artery Disease, Dyslipidemias
- What is being tested?
- a high dose of statin/ezetimib
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 1 siteSouth Korea
- Study dates
- 3 May 2023to 22 Sep 2026
- Phase
- Phase 4
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 19 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 19 years of age or older
- Patients who underwent a new generation of drug elution stent implantation for cardiovascular disease
Who cannot join
- LDL cholesterol levels below 55 mg/dL without statin treatment
- Serum AST/ALT with an acute liver disease within a month or a normal upper limit that is not continuously explained
- Allergies or overreactions to statins
- Estimated Dawn of Less than 1 Year
- If it is determined that follow-up is not possible for more than one year
- Pregnancy
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Randomized comparaTive Study Of Rosuvastatin/Ezetimibe 20/10mg and Atorvastatin/Ezetimibe 40/10mg in Patients With Coronary Artery Drug eLuting stEnt Implantation Requiring High-dose stAtin/Ezetimibe combiNaTion Therapy: TOLERANT Trial
the investigators would like to compare the differences between roschvastin and atovastatin in patients who require high-dose statin/ejetimib to undergo a new generation of drug elution stent implantation for cardiovascular disease and maintain LDL cholesterol below 55 mg/dL.
Read the detailed description
Death from vascular disease accounts for about one-third of all causes of death. Important regulatory factors in cardiovascular disease include dyslipidemia, high blood pressure, and diabetes, and keeping LDL cholesterol low among dyslipidemia levels, especially after cardiovascular stent treatment, is an essential factor to prevent another event in the future. Statin is currently the most widely used LDL cholesterol control drug with multifunctional effects such as controlling inflammatory reactions, controlling the movement and proliferation of vascular smooth muscle cells, and inhibiting the production of blood clots in addition to LDL cholesterol control.In addition, in several clinical studies, statins have shown many effects in primary and secondary prevention of cardiovascular disease, and several studies have been published that lower LDL cholesterol results in more benefits. Based on these findings, the 2016 European Heart Association (ESC), 2018 American Heart Association (ACC), and most recently changed 2022 Korean guidelines recommend controlling LDL cholesterol to <55mg/dL for patients with coronary artery disease. However, high-dose statins alone are still difficult to maintain for a long time due to increased liver levels, diabetes, and muscle pain, and recently, a drug that lowers LDL cholesterol has been developed in the small intestine called Ezetimib and is widely used in combination with statins in actual clinical trials. In fact, the RACING trial published in LANCET for domestic patients reported that the combination of moderate-intensity statins (Rosuvastatin 10mg) and ezetimib had fewer side effects for three years and better compliance, resulting in a better rate of maintaining LDL cholesterol at 70mg/dL or less than high-intensity statins alone. However, in this study, the rate at which LDL cholesterol remained below 55 mg/dL after one year was only 42% for moderate statins/esetimibe and 25% for high-intensity statins, and remained similar for three years. Therefore, high-intensity statins and ezetimibes may be essential treatments to reduce LDL cholesterol to less than 55 mg/dL and more than 50% under the current new guidelines. High-strength statins usually refer to more than 40 mg of atovastatin and 20 mg of Rosuvastatin, and drugs that combine ezetimibe with these high-strength statins are currently widely used to lower LDL cholesterol to 55 mg/dL or less if there are no special side effects in clinical practice, but research on compliance is very insufficient. This study aims to observe the rate of discontinuation or intolerance in patients taking Rosuvastatin/Ezetimib 20/10mg and Atovastatin/Ezetimib 40/10mg, with no previous comparison, RACING trial reported a 5% rate of discontinuation at rosuvastain 20mg administered, and atovatin/10mg/10mg. Referring to On the use of a pilot sample for sample size determination. the hospital conducts about 60 PCI cases a month, and about 1/5 of them are expected to be able to enroll 100 patients per group for about two years to conduct a total of 200 patients.
- Conditions
- Coronary Artery Disease, Dyslipidemias
- Being tested
- a high dose of statin/ezetimib
- Medical subject headings
- Coronary Artery Disease, Dyslipidemias
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
a high dose of statin/ezetimibDrug
In randomization, 100 patients will proceed with Rosuvastatin/Ezetimib 20/10 mg and 100 patients will proceed with Atovastatin/Ezetimib 40/10 mg.
A new generation of drug elution stents can be inserted and later registered, and if the patient agrees to participate in the study, they are randomly assigned after stent implantation.
| Study group | Role | What they receive |
|---|---|---|
| rosuvastatin/ezetimibe 20/10mg | Active comparator | rosuzet 10/20mg Receives: Drug: a high dose of statin/ezetimib |
| atorvastatin/ezetimibe 40/10mg | Active comparator | NB zet 10/40mg Receives: Drug: a high dose of statin/ezetimib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of statins changed
Percentage of statins changed to discontinuation or intolerance (muscle pain, muscle efficiency, elevated liver level, etc.) within a year
Measured: 12 months
Rate at which LDL cholesterol remains below 55 mg/dL
Rate at which LDL cholesterol remains below 55 mg/dL in all 1-year blood tests
Measured: 12 months
Secondary outcomes (12)
The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
Measured: 1 months
Cardiovascular death
Cardiovascular death
Measured: 12 months
number of non-fatal myocardial infarction
number of non-fatal myocardial infarction
Measured: 12 months
number of non-fatal stroke
number of non-fatal stroke
Measured: 12 months
number of coronary artery re-perfusion
number of coronary artery re-perfusion
Measured: 12 months
number of Newly developed diabetes or difficulty in controlling sugar
number of Newly developed diabetes or difficulty in controlling sugar
Measured: 12 months
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
Measured: 12 months
Increased muscle enzyme aberration
Increased muscle enzyme aberration (CPK > 4 x normal upper limit)
Measured: 12 months
Elevated liver enzyme levels
Elevated liver enzyme levels (AST, ALT, or both ≥ 3 x normal upper bound)
Measured: 12 months
Elevated serum creatine levels
Elevated serum creatine levels (from >50% baseline)
Measured: 12 months
number of Major bleeding
number of Major bleeding
Measured: 12 months
number of people who stopped taking the drug
number of people who stopped taking the drug
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Jun 2023
- Study start3 May 2023
- Primary completion22 Sep 2026 (estimated)
- Study completion22 Sep 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Coronary Artery DiseaseStudies of the same condition, open and under way.
- More trials run by Yonsei UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Yonsei University
- Sponsor type
- University, hospital or other
- Collaborators
- dotter
- Responsible party
- Principal investigator, Deok-Kyu Cho, Yonsei University
- Investigators
- Yongcheol Kim, MD, Study director, Yonsei University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05910476
- Sponsor's protocol ID
- 9-2023-0008
- Status last verified
- Nov 2025
- First submitted
- 31 Mar 2023
- Last updated
- 25 Nov 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 25 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized comparaTive Study Of Rosuvastatin/Ezetimibe 20/10mg and Atorvastatin/Ezetimibe 40/10mg in Patients With Coronary Artery Drug eLuting stEnt Implantation Requiring High-dose stAtin/Ezetimibe combiNaTion Therapy: TOLERANT Trial
- ClinicalTrials.gov ID
- NCT05910476
- Acronym / sponsor ID
- 9-2023-0008
- Conditions
- Coronary Artery Disease, Dyslipidemias
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Yonsei UniversityUniversity, hospital or other
- Collaborators
- dotter
- Study start
- 3 May 2023 (actual)
- Primary completion
- 22 Sep 2026 (estimated)
- Study completion
- 22 Sep 2026 (estimated)
- First posted
- 18 Jun 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
the investigators would like to compare the differences between roschvastin and atovastatin in patients who require high-dose statin/ejetimib to undergo a new generation of drug elution stent implantation for cardiovascular disease and maintain LDL cholesterol below 55 mg/dL.
Detailed description
Death from vascular disease accounts for about one-third of all causes of death. Important regulatory factors in cardiovascular disease include dyslipidemia, high blood pressure, and diabetes, and keeping LDL cholesterol low among dyslipidemia levels, especially after cardiovascular stent treatment, is an essential factor to prevent another event in the future. Statin is currently the most widely used LDL cholesterol control drug with multifunctional effects such as controlling inflammatory reactions, controlling the movement and proliferation of vascular smooth muscle cells, and inhibiting the production of blood clots in addition to LDL cholesterol control.In addition, in several clinical studies, statins have shown many effects in primary and secondary prevention of cardiovascular disease, and several studies have been published that lower LDL cholesterol results in more benefits. Based on these findings, the 2016 European Heart Association (ESC), 2018 American Heart Association (ACC), and most recently changed 2022 Korean guidelines recommend controlling LDL cholesterol to <55mg/dL for patients with coronary artery disease. However, high-dose statins alone are still difficult to maintain for a long time due to increased liver levels, diabetes, and muscle pain, and recently, a drug that lowers LDL cholesterol has been developed in the small intestine called Ezetimib and is widely used in combination with statins in actual clinical trials. In fact, the RACING trial published in LANCET for domestic patients reported that the combination of moderate-intensity statins (Rosuvastatin 10mg) and ezetimib had fewer side effects for three years and better compliance, resulting in a better rate of maintaining LDL cholesterol at 70mg/dL or less than high-intensity statins alone. However, in this study, the rate at which LDL cholesterol remained below 55 mg/dL after one year was only 42% for moderate statins/esetimibe and 25% for high-intensity statins, and remained similar for three years. Therefore, high-intensity statins and ezetimibes may be essential treatments to reduce LDL cholesterol to less than 55 mg/dL and more than 50% under the current new guidelines. High-strength statins usually refer to more than 40 mg of atovastatin and 20 mg of Rosuvastatin, and drugs that combine ezetimibe with these high-strength statins are currently widely used to lower LDL cholesterol to 55 mg/dL or less if there are no special side effects in clinical practice, but research on compliance is very insufficient. This study aims to observe the rate of discontinuation or intolerance in patients taking Rosuvastatin/Ezetimib 20/10mg and Atovastatin/Ezetimib 40/10mg, with no previous comparison, RACING trial reported a 5% rate of discontinuation at rosuvastain 20mg administered, and atovatin/10mg/10mg. Referring to On the use of a pilot sample for sample size determination. the hospital conducts about 60 PCI cases a month, and about 1/5 of them are expected to be able to enroll 100 patients per group for about two years to conduct a total of 200 patients.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| rosuvastatin/ezetimibe 20/10mg | Active comparator | Drug: a high dose of statin/ezetimibrosuzet 10/20mg |
| atorvastatin/ezetimibe 40/10mg | Active comparator | Drug: a high dose of statin/ezetimibNB zet 10/40mg |
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- 19 years of age or older
- Patients who underwent a new generation of drug elution stent implantation for cardiovascular disease
Key exclusion criteria (6 listed)
- LDL cholesterol levels below 55 mg/dL without statin treatment
- Serum AST/ALT with an acute liver disease within a month or a normal upper limit that is not continuously explained
- Allergies or overreactions to statins
- Estimated Dawn of Less than 1 Year
- If it is determined that follow-up is not possible for more than one year
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| a high dose of statin/ezetimibIn randomization, 100 patients will proceed with Rosuvastatin/Ezetimib 20/10 mg and 100 patients will proceed with Atovastatin/Ezetimib 40/10 mg. A new generation of drug elution stents can be inserted and later registered, and if the patient agrees to participate in the study, they are randomly assigned after stent implantation. | Drug | atorvastatin/ezetimibe 40/10mg, rosuvastatin/ezetimibe 20/10mg |
Primary outcome
Percentage of statins changed
Time frame: 12 months
Percentage of statins changed to discontinuation or intolerance (muscle pain, muscle efficiency, elevated liver level, etc.) within a year
Rate at which LDL cholesterol remains below 55 mg/dL
Time frame: 12 months
Rate at which LDL cholesterol remains below 55 mg/dL in all 1-year blood tests
12 secondary outcomes
The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
Time frame: 1 months
Cardiovascular death
Time frame: 12 months
number of non-fatal myocardial infarction
Time frame: 12 months
number of non-fatal stroke
Time frame: 12 months
number of coronary artery re-perfusion
Time frame: 12 months
number of Newly developed diabetes or difficulty in controlling sugar
Time frame: 12 months
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
Time frame: 12 months
Increased muscle enzyme aberration
Time frame: 12 months
Elevated liver enzyme levels
Time frame: 12 months
Elevated serum creatine levels
Time frame: 12 months
number of Major bleeding
Time frame: 12 months
number of people who stopped taking the drug
Time frame: 12 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Nov 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Yongcheol Kim, MD study director
Yonsei University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing a high dose of statin/ezetimib in people with Coronary Artery Disease and Dyslipidemias, run by Yonsei University at 1 site in South Korea.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 25 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of statins changed (time frame: 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Nov 2025.