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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.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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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.

South Korea1 site
  • Yongin Severance Hospital

    Yongin, Gyeonggi-do, 16995

Other trials in South Korea

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.

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 groups in NCT05910476
Study groupRoleWhat they receive
rosuvastatin/ezetimibe 20/10mgActive comparatorrosuzet 10/20mg
Receives: Drug: a high dose of statin/ezetimib
atorvastatin/ezetimibe 40/10mgActive comparatorNB 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.

  1. 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

  2. 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)
  1. 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

  2. Cardiovascular death

    Cardiovascular death

    Measured: 12 months

  3. number of non-fatal myocardial infarction

    number of non-fatal myocardial infarction

    Measured: 12 months

  4. number of non-fatal stroke

    number of non-fatal stroke

    Measured: 12 months

  5. number of coronary artery re-perfusion

    number of coronary artery re-perfusion

    Measured: 12 months

  6. number of Newly developed diabetes or difficulty in controlling sugar

    number of Newly developed diabetes or difficulty in controlling sugar

    Measured: 12 months

  7. 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

  8. Increased muscle enzyme aberration

    Increased muscle enzyme aberration (CPK > 4 x normal upper limit)

    Measured: 12 months

  9. Elevated liver enzyme levels

    Elevated liver enzyme levels (AST, ALT, or both ≥ 3 x normal upper bound)

    Measured: 12 months

  10. Elevated serum creatine levels

    Elevated serum creatine levels (from >50% baseline)

    Measured: 12 months

  11. number of Major bleeding

    number of Major bleeding

    Measured: 12 months

  12. 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.

  1. First posted18 Jun 2023
  2. Study start3 May 2023
  3. Primary completion22 Sep 2026 (estimated)
  4. Study completion22 Sep 2026 (estimated)

Resources

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)
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

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.

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