Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This drug is a **fixed-dose combination** of two small-molecule agents: varespladib methyl and atorvastatin. **Varespladib methyl** is an orally bioavailable prodrug rapidly converted in vivo to varespladib, which acts as a potent, selective inhibitor of secretory phospholipase A2 (sPLA2), targeting particularly the IIA, V, and X isoforms. By blocking sPLA2, varespladib methyl reduces inflammation, modulates lipid metabolism, and may have secondary antithrombotic effects. **Atorvastatin** is a well-established HMG-CoA reductase inhibitor (statin), decreasing cholesterol biosynthesis in the liver and leading to reduced LDL-cholesterol and total cholesterol. This combination was investigated primarily for **acute coronary syndrome** (ACS), aiming to address cardiovascular events by targeting both cholesterol biosynthesis and the inflammatory cascade. Large clinical trials (including VISTA-16) evaluated its effect on cardiovascular biomarkers and events, demonstrating significant reduction in LDL-C and inflammatory markers compared to atorvastatin monotherapy, but no improvement in clinical cardiovascular outcomes. Development for ACS has been discontinued[1][3][5][7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on varespladib methyl + atorvastatin.