Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**simvastatin + fenofibrate** is a fixed-dose oral combination of two lipid-modifying agents: simvastatin, a statin that inhibits HMG-CoA reductase and lowers LDL cholesterol and overall cardiovascular risk, and fenofibrate, a peroxisome proliferator-activated receptor alpha (PPARα) agonist that lowers triglycerides and increases HDL cholesterol. The combination is primarily indicated for the treatment of mixed dyslipidemia in high cardiovascular risk patients whose lipid levels are not adequately controlled with simvastatin alone. Its mechanism involves synergistic modulation of lipid metabolism pathways, leading to improved control of LDL cholesterol, triglycerides, and HDL cholesterol. The combination, unlike statin plus gemfibrozil, is not associated with a clinically relevant increase in simvastatin plasma concentrations. Clinical trials (e.g., ACCORD, SAFARI) demonstrate significant improvements in triglyceride and HDL levels and confirm safety, with the risk of serious adverse events such as myopathy only minimally increased compared to statin alone.
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 simvastatin + fenofibrate.