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A Phase III Study to Assess the Effect of FDC Laroprovstat/Rosuvastatin Compared With Laroprovstat, Rosuvastatin and Placebo on LDL-C in LLT-naïve Patients.

We're studying a new medication's impact on cholesterol levels in patients.

Recruiting
18-130 years
All
Phase 3

This study tests a new combination pill (FDC laroprovstat/rosuvastatin) to lower LDL-C, a type of bad cholesterol, in people who haven't tried cholesterol-lowering treatments (LLT) before. **Laroprovstat** is a drug that helps reduce LDL-C in the blood. **Rosuvastatin** is a commonly used medicine to lower cholesterol. **FDC** stands for Fixed-Dose Combination, meaning both drugs are in one pill. The study checks if this combination works better than taking each medicine separately or taking a placebo (a pill with no active medicine).

  • Study Length: This is a Phase III study, indicating it's in the final stages before approval.
  • Eligibility: Participants must be 18 or older, have low estimated heart disease risk, and not have used LLT recently.
  • Exclusion: People of Asian origin, those with severe uncontrolled health issues, or who can't tolerate statins cannot join.
Study details
    Hypercholesterolaemia

NCT07619131

AstraZeneca

11 October 2026

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Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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