- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
41 result(s) found for: Cardiovascular Diseases AND Cholesterol, LDL AND ezetimibe.
Displaying page 1 of 3.
| EudraCT Number: 2016-003281-84 | Sponsor Protocol Number: EXCRETE | Start Date*: 2018-03-27 |
| Sponsor Name:Academical Medical Centre, department of internal | ||
| Full Title: The Effect of UrsodeoXyCholicacid (UDCA) and ezetimibe on total faecal steRol ExcreTion and plasma lipid lEvels | ||
| Medical condition: Familial hypercholesterolemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004556-30 | Sponsor Protocol Number: LPS15021 | Start Date*: 2018-08-24 | |||||||||||
| Sponsor Name:Sanofi-Aventis Groupe | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-blind, Active-controlled Clinical Trial to Evaluate the Efficacy and Safety of a New Formulation of Zenon (Ezetimibe/Rosuvastatin Fixed Dose Combination) in Patien... | |||||||||||||
| Medical condition: Patients with Primary Hypercholesterolaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) CZ (Completed) BG (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006550-31 | Sponsor Protocol Number: SEC-ES-BempeDACS-2021 | Start Date*: 2022-04-05 |
| Sponsor Name:SPANISH SOCIETY OF CARDIOLOGY | ||
| Full Title: Efficacy and Security of BempeDoic acid in Acute Coronary Syndrome | ||
| Medical condition: Acute coronary syndrome with poor LDL-cholesterol control | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-005513-35 | Sponsor Protocol Number: MK-0653A Protocol 809-00 | Start Date*: 2007-02-05 | |||||||||||
| Sponsor Name:Laboratoires Merck Sharp & Dohme - Chibret | |||||||||||||
| Full Title: A Randomized, Double-Blind, Active-Controlled, Multicenter Study to Assess the LDL-C Lowering of Switching to a Combination tablet Ezetimibe/Simvastatin (10mg/20mg) compared to Rosuvastatin 10mg in... | |||||||||||||
| Medical condition: Adjunctive therapy to diet for the reduction of elevated total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (Apo B), triglycerides (TG), and non-high-density lipo... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) EE (Completed) LT (Completed) CZ (Completed) PT (Completed) LV (Completed) IT (Completed) GR (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000935-29 | Sponsor Protocol Number: 20120332 | Start Date*: 2014-02-03 | |||||||||||
| Sponsor Name:Amgen Inc. | |||||||||||||
| Full Title: A Double-blind, Randomized, Multicenter Study to Evaluate the Safety and Efficacy of AMG 145, Compared With Ezetimibe, in Hypercholesterolemic Subjects Unable to Tolerate an Effective Dose of a HMG... | |||||||||||||
| Medical condition: Hypercholesterolemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) GB (Completed) IT (Completed) DK (Completed) NL (Completed) NO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004084-39 | Sponsor Protocol Number: 1002-048 | Start Date*: 2017-04-19 | ||||||||||||||||
| Sponsor Name:Esperion Therapeutics Inc., | ||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Bempedoic Acid (ETC-1002) 180 mg/day as Add-on to Ezetimibe Therapy in Patie... | ||||||||||||||||||
| Medical condition: This study is to assess the efficacy of bempedoic acid 180 mg/day versus placebo in decreasing low-density lipoprotein cholesterol (LDL-C) when added to ezetimibe therapy in patients with high LDL-... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) GB (Completed) DE (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-001109-29 | Sponsor Protocol Number: CKJX839D12304 | Start Date*: 2022-12-06 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A Double-blind, Randomized, Placebo- and Active-Comparator Controlled Study to Evaluate the Efficacy of Inclisiran as Monotherapy in Patients with Primary Hypercholesterolemia Not Receiving Lipid-L... | |||||||||||||
| Medical condition: Primary Hypercholesterolemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004130-34 | Sponsor Protocol Number: EFC11569 | Start Date*: 2012-10-17 | |||||||||||
| Sponsor Name:sanofi-aventis Recherche & Développement | |||||||||||||
| Full Title: A Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy and Safety of SAR236553/REGN727 Versus Ezetimibe in High Cardiovascular Risk Patients With Hypercholesterolemia Not Adequat... | |||||||||||||
| Medical condition: Hypercholesterolaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DK (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003526-50 | Sponsor Protocol Number: HACOL-ACS | Start Date*: 2023-05-09 | ||||||||||||||||
| Sponsor Name:Hannover Medical School | ||||||||||||||||||
| Full Title: A prospective, interventional, single-center, single-arm study to assess the effectiveness of Bempedoic acid to achieve LDL-cholesterol targets in patients following ST-elevation or Non-ST-elevatio... | ||||||||||||||||||
| Medical condition: Patients following acute percutaneous coronary intervention for STEMI or NSTEMI insufficiently treated with high-intensity oral lipid lowering therapy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-000622-55 | Sponsor Protocol Number: I5S-MC-EFJE | Start Date*: 2013-07-31 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 2 Efficacy and Safety Dose-Ranging Study of LY3015014 in Patients with Primary Hypercholesterolemia | |||||||||||||
| Medical condition: Primary hypercholesterolaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) NL (Completed) PL (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001934-19 | Sponsor Protocol Number: LPS14354 | Start Date*: 2016-02-15 | |||||||||||
| Sponsor Name:Sanofi-Aventis Groupe | |||||||||||||
| Full Title: A Randomized, Open-Label, Parallel Group Study to Evaluate the Efficacy and Safety of Alirocumab Versus Usual Care in Patients with Type 2 Diabetes and Mixed Dyslipidemia at High Cardiovascular Ris... | |||||||||||||
| Medical condition: Dyslipidemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DE (Completed) GB (Completed) SE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001846-90 | Sponsor Protocol Number: MDCO-PCS-17-08 | Start Date*: 2017-12-12 | |||||||||||
| Sponsor Name:The Medicines Company | |||||||||||||
| Full Title: A PLACEBO-CONTROLLED, DOUBLE-BLIND, RANDOMIZED TRIAL TO EVALUATE THE EFFECT OF 300 MG OF INCLISIRAN SODIUM GIVEN AS SUBCUTANEOUS INJECTIONS IN SUBJECTS WITH ATHEROSCLEROTIC CARDIOVASCULAR DISEASE (... | |||||||||||||
| Medical condition: Hypercholesterolemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) GB (Completed) CZ (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004393-22 | Sponsor Protocol Number: LIB003-006 | Start Date*: 2022-01-13 | |||||||||||
| Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
| Full Title: Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Long-Term Efficacy and Safety of LIB003 in Patients With Cardiovascular Disease, or at High Risk for Cardiovascular Disea... | |||||||||||||
| Medical condition: Patients With Cardiovascular Disease or at High Risk for Cardiovascular Disease, on Stable Lipid-Lowering Therapy Requiring Additional Low-Density Lipoprotein Cholesterol Reduction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NO (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002472-30 | Sponsor Protocol Number: MDCO-PCS-17-03 | Start Date*: 2018-01-04 | |||||||||||
| Sponsor Name:The Medicines Company | |||||||||||||
| Full Title: A PLACEBO-CONTROLLED, DOUBLE-BLIND, RANDOMIZED TRIAL TO EVALUATE THE EFFECT OF 300 MG OF INCLISIRAN SODIUM GIVEN AS SUBCUTANEOUS INJECTIONS IN SUBJECTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEM... | |||||||||||||
| Medical condition: Hypercholesterolemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) CZ (Completed) SE (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005065-40 | Sponsor Protocol Number: TA-8995-302 | Start Date*: 2022-05-13 | ||||||||||||||||||||||||||
| Sponsor Name:NewAmsterdam Pharma B.V. | ||||||||||||||||||||||||||||
| Full Title: Obicetrapib on Top of Maximum Tolerated Lipid-Modifying Therapies (BROADWAY): A Placebo-Controlled, Double-Blind, Randomized Phase 3 Study to Evaluate the Effect of 10 mg Obicetrapib in Participant... | ||||||||||||||||||||||||||||
| Medical condition: dyslipidemia heterozygous familial hypercholesterolemia (HeFH) atherosclerotic cardiovascular disease (ASCVD) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Completed) DK (Completed) CZ (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-004392-40 | Sponsor Protocol Number: LIB003-005 | Start Date*: 2021-12-21 | |||||||||||
| Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
| Full Title: Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Long-Term Efficacy and Safety of LIB003 in Patients With Cardiovascular Disease on Stable Lipid-Lowering Therapy Requirin... | |||||||||||||
| Medical condition: Patients With Cardiovascular Disease on Stable Lipid-Lowering Therapy Requiring Additional Low-Density Lipoprotein Cholesterol Reduction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NO (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001221-27 | Sponsor Protocol Number: R727-CL-1119 | Start Date*: 2013-03-20 | |||||||||||
| Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Double-Dummy, Active-Controlled Study to Evaluate the Efficacy and Safety of REGN727/SAR236553 in Patients with Primary Hypercholesterolemia Who are Intolerant to Statins | |||||||||||||
| Medical condition: Patients with primary hypercholesterolemia and moderate, high or very high cardiovascular (CV) risk who are intolerant to statins | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) IT (Completed) GB (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002871-20 | Sponsor Protocol Number: LIB003-012 | Start Date*: 2022-04-21 | |||||||||||
| Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
| Full Title: Randomized, Open Label, Phase 3 Study to Evaluate the Efficacy and Safety of Lerodalcibep (LIB003) compared to Inclisiran in Patients With Cardiovascular Disease, or at High Risk for Cardiovascula... | |||||||||||||
| Medical condition: Patients with atherosclerotic cardiovascular (CV) disease (ASCVD) or high risk of ASCVD who need additional LDL-C reduction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) NO (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001446-25 | Sponsor Protocol Number: FHGT002 | Start Date*: 2017-09-20 |
| Sponsor Name:University of Pennsylvania | ||
| Full Title: AAV8-mediated Low Density Lipoprotein Receptor (LDLR) Gene Replacement in Subjects with Homozygous Familial Hypercholesterolemia (HoFH) | ||
| Medical condition: Adults with homozygous familial hypercholesterolemia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003092-55 | Sponsor Protocol Number: MDCO-PCS-17-05 | Start Date*: 2019-02-05 | |||||||||||
| Sponsor Name:The Medicines Company | |||||||||||||
| Full Title: A long term extension trial of the Phase III lipid-lowering trials to assess the effect of long term dosing of inclisiran given as subcutaneous injections in subjects with high cardiovascular risk ... | |||||||||||||
| Medical condition: Hypercholesterolemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) DE (Completed) SE (Completed) DK (Completed) HU (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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