Condition: Mixed Dyslipidemia · Hypercholesterolaemia · Sponsor: A. Menarini International Licensing S.A.
This Phase 3, randomized, double-blind, active-controlled study evaluates the efficacy and safety of obicetrapib (OBI) compared to bempedoic acid (BPA) in participants with dyslipidemia at high or very high cardiovascular risk. Participants must have elevated low density lipoprotein cholesterol (LDL-C) levels despite receiving maximally tolerated lipid lowering therapy. The primary objective is to compare the LDL-C lowering effect of OBI (a CETP inhibitor) against BPA at 12 weeks
This description comes directly from the study's public registry record.
Andrea Conte, Medical Doctor · +352 26497650 · aconte@menarini.lu
Always discuss trial participation with your own doctor first.
| FutureMeds North Tees | Stockton-on-Tees, United Kingdom | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07614958