Three cholesterol drugs better than two for diabetics?
NCT ID NCT07255820
First seen Jun 26, 2026 · Last updated Jul 22, 2026 · Updated 2 times
Summary
This study tests whether taking three cholesterol-lowering drugs together works better than taking two in people with type 2 diabetes and high LDL cholesterol. 126 adults aged 35-60 will be split into three groups: one gets rosuvastatin plus ezetimibe, another gets bempedoic acid plus ezetimibe, and the third gets all three drugs. The goal is to see which combination lowers LDL cholesterol most safely over 12 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Rosuvastatin, Ezetimibe, Bempedoic Acid
- What this could lead to
- If triple therapy works better, it could offer a more effective way to lower cholesterol in people with diabetes, reducing heart disease risk.
- What could go wrong
- This is a small, short-term study (12 weeks) with only 126 participants. Results may not apply to everyone, and adding a third drug could increase side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
126 people
The number who actually took part.
- Started
-
Jan 2026
- Finished
-
Jun 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
35 to 60 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Males and females * Age 35-60 years * HbA1c ≥ 7.0 (≥ 48 mmol/mol) * On stable anti-diabetic therapy for at least 3 months * LDL-C \> 100 mg/dL on at least two occasions * Diagnosed with hypercholesterolemia * Establish high cardiovascular risk (e.g, previous MI, stroke or atherosclerosis) or * ≥2 cardiovascular risk factors (hypertension, smoking, obesity, family history) * BMI \>23 - \<32(WHO Asian Criteria) * No prior statin side effects Exclusion Criteria: * HbA1c \>10 % (86 mmol/mol) * BMI \> 32 * Type 1 Diabetes, gestational diabetes * Pregnancy or lactation * Acute liver disease or ALT/AST levels \> 3× the upper limit of normal * Renal failure (GFR \< 30 mL/min) * Uncontrolled hypothyroidism or nephrotic syndrome * Recent cancer diagnosis (last 6 months) * Current use of other lipid-lowering agents (e.g., fibrates or PCSK9 inhibitors) * Known allergy to any component * Statin intolerance with severe adverse effects (e.g., rhabdomyolysis)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
National Medical Center
Karachi, Sindh, 75500, Pakistan
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