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RECRUITING
NCT07614958
PHASE3

Phase 3 Clinical Study Evaluating Efficacy, Safety, and Tolerability of Obicetrapib Vs Bempedoic Acid to Treat Dyslipidemia in Adults With Primary Non-familial Hypercholesterolemia or Mixed Dyslipidemia at High to Very High Cardiovascular Risk, During a Treatment Period of Approximately 84 Days

Sponsor: A. Menarini International Licensing S.A.

View on ClinicalTrials.gov

Summary

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

Official title: A Double-Blind, Randomized, Comparative Study of Obicetrapib and Bempedoic Acid on Top of Maximally Tolerated Lipid-Lowering Therapy in Patients With Dyslipidemia at High to Very High Cardiovascular Risk

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

426

Start Date

2026-05-06

Completion Date

2027-01

Last Updated

2026-06-09

Healthy Volunteers

No

Interventions

DRUG

Obicetrapib 10 mg/Bempedoic Acid Placebo

Orally, Once Daily

DRUG

Bempedoic Acid 180mg/Placebo Obicetrapib

Orally, Once Daily

Locations (1)

FutureMeds North Tees

Stockton-on-Tees, United Kingdom