Impact of Obicetrapib and Obicetrapib Plus Repatha on Lp(a) Levels
A Phase 2 Study to Evaluate the Effect of Obicetrapib Alone and in Combination With Evolocumab (Repatha®) on Lipoprotein (a) in Patients With Mild Dyslipidemia: The VINCENT Study
NewAmsterdam Pharma
69 participants
Dec 2, 2024
INTERVENTIONAL
Conditions
Summary
The goal of this open label 16 week trial is to evaluate Lp(a) levels for patients with elevated Lp(a) being treated with obicetrapib and obiceptrapib/evolocumab Patients will: Have baseline Lp(a) tested at randomization Take 10mg/dL obiceptrapib daily for 8 weeks and have Lp(a) tested at Week 8 Take 10 mg/dL obicetrapib daily/evolocumab 140 every other week for 8 weeks and have Lp(a) retested at Week 16
Eligibility
Inclusion Criteria3
- Lp(a): >=50 mg/dL (>=125 nmol/L) for cohort 1 (FILLED) and Lp(a) >= 20 mg/dL (>= 50 nmol/L) to <50 mg/dL (< 125 nmol/L) for cohort 2
- LDL-C >70 mg/dL
- TG < 400mg/dL (<4.52 mmol/L)
Exclusion Criteria2
- HbA1c>=10 or FPG >=270 mg/dL
- CV events within 3 months of screen
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Interventions
10 mg obicetrapib for 8 weeks followed by 10 mg obicetrapib/ 140 mg evolocumab (every 2 weeks) combination for 8 weeks
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06496243