Study of Obicetrapib & Ezetimibe Fixed Dose Combination on Top of Maximum Tolerated Lipid-Modifying Therapies
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- NewAmsterdam Pharma
- Study ID
- NCT06005597
- Phase
- PHASE3
- Status
- Completed
Conditions
- ASCVD
- Dyslipidemias
- Familial Hypercholesterolemia
- High Cholesterol
- Hypercholesterolemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Combination Therapy — COMBINATION_PRODUCTtablet; 10mg obicetrapib and 10mg ezetimibe fixed does combination
- Monotherapy obicetrapib — DRUGtablet; 10mg obicetrapib
- Monotherapy ezetimibe — DRUGcapsule; 10mg ezetimibe
- Combination Therapy placebo — OTHERtablet; no active ingredient
- Obicetrapib Placebo — OTHERtablet; no active ingredient
- Ezetimibe Placebo — OTHERcapsule; no active ingredient
Study Details
The study is a placebo-controlled, double-blind, randomized, phase 3 study in participants with heterozygous familial hypercholesterolemia (HeFH) and/or atherosclerotic cardiovascular disease (ASCVD) or multiple ASCVD risk factors to evaluate the efficacy, safety and tolerability of obicetrapib 10mg and ezetimibe 10mg fixed dose combination as an adjunct to diet and maximally tolerated lipid-lowering therapy.
Key Dates
- Start date
- Mar 1, 2024
- Status verified
- Sep 2025
- Primary completion
- Sep 25, 2024
- Completion
- Oct 16, 2024
Study Design
- Enrollment
- 407 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Combination Therapyonce-daily obicetrapib 10 mg and ezetimibe 10 mg fixed dose combination tablet, placebo tablet, placebo capsule
- Experimental: Monotherapy obicetrapibonce-daily obicetrapib 10 mg, placebo tablet, placebo capsule
- Active Comparator: Monotherapy ezetimibeonce-daily ezetimibe 10 mg capsule, 2 placebo tablets
- Placebo Comparator: Placeboonce-daily placebo tablets (2), placebo capsule
Primary Outcome Measure
Effect of Fixed-Dose Combination (FDC) Compared to Placebo on LDL-C [ Time Frame: 84 Days ]
Locations (45)
Related coverage on Hipa.ai
- Obicetrapib/Ezetimibe Combo Reduces LDL-C by 45.58% in Dyslipidemia TrialObicetrapib · Oct 8, 2025 · ClinicalTrials.gov
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