跳至主要内容
临床试验/EUCTR2006-006219-56-GB
EUCTR2006-006219-56-GB进行中(未招募)1 期

A multicentre, double-blind, randomised, parallel-group study to evaluate the efficacy, safety and tolerability of ezetimibe/simvastatin 10/40mg, atorvastatin 40mg, and rosuvastatin 10mg to achieve an LDL-C level of <2mmol/l in patients with established CVD or at high risk” of developing CVD, currently treated with simvastatin 40mg and with a fasting LDL-C ?2 mmol/l

Merck & Co Inc.,0 个研究点目标入组 800 人开始时间: 2007年2月12日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
800

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

入选标准

  • 1.Patient is male or female and aged over 18
  • 2.Patient provides written informed consent
  • 3.Patient has a fasting LDL-C level ?2mmol/l at both visit 1 and again at visit 2
  • 4.Patient has established CVD, diabetes or at high risk” of CVD (>20 % risk over 10 years, Framingham scale)
  • 5.Patient has taken simvastatin 40mg continuously for the past 6 weeks
  • 6.Patient has a fasting triglyceride level of <3.7mmol/l
  • 7.Patient has HbA1C ?9% at visit 1
  • 8.Patient is 75% compliant with medication between visit 1 and visit 2
  • 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

  • 1.Patient is hypersensitive to any of the study medications or their components
  • 2.Patient has a history of, or active liver disease (persistent elevation of ALT / AST (>3xULN)
  • 3.Patient is pregnant, lactating, or a female patient of childbearing potential not using adequate contraception
  • 4.Patient has severe renal impairment: creatinine clearance <30ml/min (Cockcroft-Gault equation) (in patients with moderate renal impairment: <60ml/min, the dose of rosuvastatin will be 5mg in line with the SPC)
  • 5.Patient has uncontrolled endocrine or metabolic disease known to influence serum lipids or lipoproteins (i.e. secondary causes of hyperlipidaemia such as hypothyroidism or hyperthyroidism)
  • 6.Patient has a recent history of, or current, alcohol abuse
  • 7.Patient has CK >10 x ULN at visit 1 or visit 2
  • 8.Patient has fasting LDL-C >4.2mmol/l
  • 9.Patient has any acute or serious condition, or history suggestive of myopathy or predisposing to the development of renal failure secondary to rhabdomyolysis (e.g. sepsis, hypotension, major surgery, trauma, severe metabolic, severe endocrine and electrolyte disorders or uncontrolled seizures).

研究者

相似试验

进行中(未招募)
1 期
Phase III study to assess efficacy and safety of D9421-C 9 mg with active Crohn’s Disease in Japa
EUCTR2014-004132-20-Outside-EU/EEAAstraZeneca K.K.112
进行中(未招募)
1 期
Study of safety and efficacy of Hercules versus Herceptin® in patients with breast cancerHuman Epidermal Growth Factor Receptor 2 positive (HER2+) metastatic breast cancer (MBC)MedDRA version: 17.0Level: LLTClassification code 10027475Term: Metastatic breast cancerSystem Organ Class: 100000004864
EUCTR2011-001965-42-BGMYLAN GmbH600
进行中(未招募)
1 期
Study to assess the efficacy and safety of investigational product, P-3074 cutaneous spray, solution, in the treatment of male pattern baldness.Androgenetic alopecia
EUCTR2015-002877-40-DEPolichem S.A.458
进行中(未招募)
1 期
Study to assess the efficacy and safety of investigational product, P-3074 cutaneous spray, solution, in the treatment of male pattern baldness.MedDRA version: 19.0Level: PTClassification code 10068168Term: Androgenetic alopeciaSystem Organ Class: 10040785 - Skin and subcutaneous tissue disordersAndrogenetic alopecia
EUCTR2015-002877-40-ESPolichem S.A.450
进行中(未招募)
1 期
A multicentre, randomized, double-blind, parallel-group, placebo-controlled, dose-ranging study to evaluate the efficacy, safety and tolerability of once daily oral dosing of GW501516 (2.5 mg, 5 mg and 10 mg) over 12 weeks in subjects withprimary hypercholesterolemia on background statin therapy.primary hypercholesterolemiaMedDRA version: 8.1Level: LLTClassification code 10020604Term: Hypercholesterolemia
EUCTR2006-002911-28-NLGlaxoSmithKline R&D