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Active (not recruiting) Phase 3 NCT05202509

Cardiovascular Outcome Study to Evaluate the Effect of Obicetrapib in Patients With Cardiovascular Disease

Phase 3 – large-scale trial before approval
Conditions: Atherosclerotic Cardiovascular Disease

Sponsor: NewAmsterdam Pharma

trial.available_in: БГ
Overview
This study will be a placebo-controlled, double-blind, randomized, phase 3 study in participants with Atherosclerotic Cardiovascular Disease (ASCVD) who are not adequately controlled despite maximally tolerated lipid-lowering therapy.
Description
This study will be a placebo-controlled, double-blind, randomized, phase 3 study to evaluate the effect of 10mg Obicetrapib in participants with Atherosclerotic Cardiovascular Disease (ASCVD) who are not adequately controlled despite maximally tolerated lipid-lowering therapy to reduce the risk of cardiovascular death, myocardial infarction, stroke and non-elective coronary revascularization. The PREVAIL Study
Who can participate
Inclusion Criteria: * Males \& females ≥ 18 years age. * Established ASCVD including: * Coronary artery disease * Cerebrovascular disease * Peripheral Artery disease * On maximally tolerated lipid-modifying therapy * Fasting LDL-C ≥ 55 mg/dL * Fasting triglycerides \< 400 mg/dL * Estimated glomerular filtration rate ≥ 30 mL/min Exclusion Criteria: * New York Heart Association class III or IV heart failure or left ventricular ejection fraction \< 30% * Have been hospitalized for Heart Failure within 5 years prior to screening * Had non-fatal MI, non-fatal stroke, non-elective coronary revascularization and/or hospitalization for unstable angina or chest pain within past 3 months prior to screening * Uncontrolled hypertension * Diagnosis of homozygous familial hypercholesterolemia (HoFH) * Active liver disease * HbA1c ≥10% * Thyroid Stimulating Hormone (TSH) \> 1.5 times upper limit normal * Creatine kinase \> 3 times upper limit normal * History of malignancy with surgery in past 3 years * History of alcohol or drug abuse within past 5 years * Received treatment with investigational product or device within past 30 days excluding Coronavirus treatment or vaccine * Known allergy to study drug * Participated in previous obicetrapib trial * Taking gemfibrozil within 30 days screening
Locations 22
Australia (1)
Royal Adelaide Hospital
Adelaide
Bulgaria (1)
MHAT Aytos EOOD Department of Internal Diseases
Aytos
Canada (1)
Medical Arts Health Research Group - Kamloops
Kamloops , British Columbia
China (1)
Peking University First Hospital
Beijing
Croatia (1)
General Hospital Karlovac
Karlovac
Czech Republic (1)
Hornicka nemocnice s poliklinikou Bilina s.r.o.
Bílina
Denmark (1)
Aalborg University Hospital
Aalborg
Finland (1)
StudyCor Oy
Jyväskylä
Georgia (1)
Health Ltd
Batumi
Hungary (1)
Lausmed Kft
Baja
Israel (1)
Barzilai Medical Center
Ashkelon
Italy (1)
Azienda Ospedaliero-Universitaria di Ferrara-Arcispedale Sant'Anna
Ferrara
Japan (1)
Chiba University Hospital
Chiba
Jordan (1)
Abdali Hospital
Amman
Latvia (1)
Latgales Medical Center
Daugavpils
Netherlands (1)
Academic Medical Center - Department of Vascular Medicine
Amsterdam
Poland (1)
CENTRUM MEDYCZNE INTERCOR Sp. z o.o.
Bydgoszcz
Slovakia (1)
Stredoslovensky ustav srdcovych a cievnych chorob, a.s.
Banská Bystrica
South Africa (1)
Iatros International
Bloemfontein
Spain (1)
Hospital Universitario de A Coruna
A Coruña
United Kingdom (1)
Atlantic Medical Group
Penzance , Cornwall
United States (1)
Advanced Cardiovascular LLC
Alexander City , Alabama
Technical details
Status
Active (not recruiting)
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
07.02.2022
Completion date
01.11.2026
Registry ID
NCT05202509
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.