跳至主要内容
临床试验/EUCTR2005-005093-70-DE
EUCTR2005-005093-70-DE进行中(未招募)不适用

A Worldwide, Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the Lipid-Altering Efficacy, Safety and Tolerability of MK-0524A in Patients With Primary Hypercholesterolemia or Mixed Hyperlipidemia - MK-0524A Lipid/Flushing Study

MSD SHARP & DOHME GMBH0 个研究点目标入组 1,620 人开始时间: 2005年11月25日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,620

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patient has a history of primary hypercholesterolemia or mixed hyperlipidemia.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patient has a history or current evidence of any condition, therapy, or lab abnormality that might confound the results of the study, interfere with the patient’s participation for the full duration of the study, or is not in the best interest of the patient to participate.

研究者

相似试验

进行中(未招募)
不适用
A Worldwide, Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the Lipid-Altering Efficacy, Safety and Tolerability of MK-0524A in Patients With Primary Hypercholesterolemia or Mixed Hyperlipidemia - MK-0524A Lipid/Flushing StudyHypercholesterolaemiaMedDRA version: 8.0Level: LLTClassification code 10020603
EUCTR2005-005093-70-ATMerck Sharp & Dohme GesmbH1,620
已完成
不适用
A Worldwide, Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the Long-term Efficacy, Safety and Tolerability of ERN/LRPT in Patients With Dyslipidemia-E78 Disorders of lipoprotein metabolism and other lipidaemiasDisorders of lipoprotein metabolism and other lipidaemiasE78
PER-108-09MERCK SHARP & DOHME PERU S.R.L.,
进行中(未招募)
不适用
A Worldwide, Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the Long-term Efficacy, Safety and Tolerability of Extended-Release (ER) Niacin and Laropiprant (ERN/LRPT) in Patients with DyslipidemiaDyslipidemiaMedDRA version: 12.0Level: LLTClassification code 10058108Term: Dyslipidaemia
EUCTR2009-012772-27-DKMerck & Co., Inc.1,125
进行中(未招募)
不适用
A worldwide placebo-controlled study to evaluate the additional lipid benefits of extended release (ER) niacin/laropiprant when taken with current lipid-modifying therapy in individuals with abnormal lipidsPrimary Hypercholesterolemia or Mixed DyslipidemiaMedDRA version: 14.1Level: LLTClassification code 10020604Term: HypercholesterolemiaSystem Organ Class: 100000004861MedDRA version: 14.1Level: LLTClassification code 10058110Term: DyslipidemiaSystem Organ Class: 100000004861
EUCTR2010-021627-27-DEMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.1,224
进行中(未招募)
不适用
A Worldwide, Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the Long-term Efficacy, Safety and Tolerability of Extended-Release (ER) Niacin and Laropiprant (ERN/LRPT) in Patients with DyslipidemiaDyslipidemiaMedDRA version: 12.0Level: LLTClassification code 10058108Term: Dyslipidaemia
EUCTR2009-012772-27-FIMSD Finland Oy1,125