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Hyperlipoproteinemia Type II clinical trials

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NCT ID: NCT03694197 Terminated - Clinical trials for Heterozygous Familial Hypercholesterolemia

Long Term Safety Study of PRALUENT

Start date: September 28, 2018
Phase: Phase 4
Study type: Interventional

The primary objective of the study was to evaluate the long term safety of PRALUENT in participants with heterozygous familial hypercholesterolemia (heFH) or non-familial hypercholesterolemia (FH) participants at high or very high cardiovascular risk who completed the neurocognitive function study R727-CL-1532 (NCT02957682). The secondary objectives of the study were: - To evaluate the effect of PRALUENT on low-density lipoprotein cholesterol (LDL-C) - To evaluate the effect of PRALUENT on other lipid parameters - To evaluate the effect of PRALUENT on gonadal steroid hormones

NCT ID: NCT03331666 Terminated - Clinical trials for Familial Hypercholesterolemia

Impact of LDL-cholesterol Lowering on Platelet Activation

Start date: November 16, 2018
Phase: Phase 4
Study type: Interventional

The primary goal is to assess the impact of Evolocumab therapy on platelet function of familial hypercholesterolemia (FH) patients in a randomized, double blind study. Evolocumab is a humanized monoclonal antibody that targets circulating PCSK9, increases hepatic LDL receptor, decreases plasma LDL cholesterol and reduces risk of cardiovascular events. Evolocumab (brand name Rapatha) has been approved by FDA along with diet and maximally tolerated statin therapy in adults with FH or atherosclerotic heart or blood vessel problems, who need additional lowering of LDL cholesterol. The secondary goal is to determine if platelet activation or the response to Evolocumab therapy is modified by rs3184504 polymorphism. The investigators believe that these investigations will complement ongoing studies to demonstrate that Evolocumab reduces athero-thrombotic risk and aid the decision-making as to whether Evolocumab can reduce the atherothrombotic risk in acute coronary syndrome (ACS) patients.

NCT ID: NCT02651675 Terminated - Clinical trials for Homozygous Familial Hypercholesterolemia (HoFH)

A Gene Therapy Study for Homozygous Familial Hypercholesterolemia (HoFH)

Start date: March 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This first-in-human study is intended to evaluate the safety and preliminary effectiveness of AAV (Adeno-associated virus)-based liver-directed gene therapy in the treatment of adults with Homozygous Familial Hypercholesterolemia (HoFH).

NCT ID: NCT02013713 Terminated - Clinical trials for Familial Hypercholesterolemia

French Observatory of Familial Hypercholesterolemia in Cardiology

FH Care
Start date: November 2014
Phase:
Study type: Observational

The Family Hypercholesterolemia remains poorly diagnosed disease with an outlet sometimes suboptimal care. However, the Family Hypercholesterolemia exposes patients concerned at increased cardiovascular risk. The frequency of familial hypercholesterolemia in cardiologic is little studied and remains unknown, and there is little data on the profile of patients, diagnostic methods and management. Main objectives: - Establish a monitoring patients with hypercholesterolemia Family cardiology in France - Characterize the Family hypercholesterolemia in cardiology, including assessing the frequency of the most severe forms, which are at higher cardiovascular risk.

NCT ID: NCT01841684 Terminated - Clinical trials for Homozygous Familial Hypercholesterolemia

Efficacy and Tolerability of Anacetrapib Added to Ongoing Lipid-Lowering Therapy in Adult Participants With Homozygous Familial Hypercholesterolemia (HoFH) (MK-0859-042)

Start date: June 2013
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and effect of anacetrapib on low-density lipoprotein-cholesterol (LDL-C) when added to ongoing lipid-lowering therapy. The primary hypothesis is that treatment with anacetrapib 100 mg for 12 weeks will lower LDL-C to a greater extent than treatment with placebo.

NCT ID: NCT01583647 Terminated - Clinical trials for Heterozygous Familial Hypercholesterolemia

A Study of Extended-release (ER) Niacin/Laropiprant in Adolescents With Heterozygous Familial Hypercholesterolemia (MK-0524A-158)

Start date: June 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the pharmacokinetics of laropiprant following administration of a single dose of 1 (Panel A) and 2 (Panel B) combination tablets of MK-0524A in adolescents with heterozygous familial hypercholesterolemia.

NCT ID: NCT01410383 Terminated - Clinical trials for Heterozygous Familial Hypercholesterolaemia

Efficacy and Safety Study of Eprotirome in HeFH Patients Who Are on Optimal Standard of Care

AKKA
Start date: October 2011
Phase: Phase 3
Study type: Interventional

Eprotirome is a liver selective thyroid hormone that can reduce several independent risk factors for cardiovascular disease, while an euthyroid state is preserved in the extrahepatic tissue. The purpose of this Phase III study is to assess the long-term efficacy and safety of Eprotirome in Patients with heterozygous Familial Hypercholesterolaemia who are on optimal standard of care.

NCT ID: NCT00384293 Terminated - Clinical trials for Hypercholesterolemia, Familial

Carotid IMT (Intima Media Thickening) Study (0524A-041)(TERMINATED)

ACHIEVE
Start date: September 2006
Phase: Phase 3
Study type: Interventional

This is a 105-week clinical study in patients with heterozygous familial hypercholesterolemia on intensive Low Density Lipoprotein-cholesterol (LDL-C) lowering therapy intended to assess the affects of MK0524A on carotid intima media thickening using ultrasound compared to patients taking placebo. There will be 12 scheduled clinic visits involving review of medical history, physical exam, vital signs, laboratory testing, ultrasound imaging, and electrocardiograms.

NCT ID: NCT00263081 Terminated - Clinical trials for Hypercholesterolemia

Efficacy of Lapaquistat Acetate Co-Administered With Current Lipid-Lowering Treatment on Blood Cholesterol Levels in Subjects With Homozygous Familial Hypercholesterolemia

Start date: November 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the efficacy of lapaquistat acetate, once daily (QD), to lower cholesterol in subjects with homozygous familial hypercholesterolemia undergoing lipid-lowering treatment.

NCT ID: NCT00151788 Terminated - Atherosclerosis Clinical Trials

Efficacy and Safety of the ACAT Inhibitor CS-505 (Pactimibe) for Reducing the Progression of Carotid Artery Disease. This Study is Also Known as CAPTIVATE.

Start date: February 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The effects of pactimibe versus placebo on the progression of atherosclerosis in the carotid arteries will be assessed using standard ultrasound techniques.