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临床试验/EUCTR2017-002297-39-IT
EUCTR2017-002297-39-IT进行中(未招募)1 期

An Open-Label Study to Evaluate the Efficacy and Safety of Alirocumab in Children and Adolescents with Homozygous Familial Hypercholesterolemia

Sanofi-Aventis Recherche & Développement0 个研究点目标入组 18 人开始时间: 2018年5月23日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
18

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

  • -Patients genetically diagnosed with homozygous familial hypercholesterolemia (hoFH).
  • -Patients treated with optimal dose of statin +/- other lipid modifying therapies (LMTs), or non-statin LMTs if statin-intolerant at stable dose(s) for at least 4 weeks prior to screening lipid sample.
  • -A signed informed consent indicating parental permission with or without patient assent.
  • -For patients on apheresis, currently undergoing stable low-density lipoprotein (LDL) apheresis therapy prior to the screening and have initiated apheresis treatment for at least 6 months.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 50
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Patients with low-density lipoprotein - cholesterol (LDL-C) less than 130 mg/dL (3.37 mmol/L) obtained during the screening period after the patient has been on stable apheresis procedure or lipid modifying therapy (LMT) (i.e., stable optimal dose of statin ± other stable LMTs, or stable non statin LMTs in statin-intolerant patients) treatment for at least 4 weeks.
  • -Patients with body weight less than 25 kg.
  • -Patients aged 8 to 9 years not at Tanner Stage 1 and patients aged of 10 to 17 years not at least at Tanner Stage 2 in their development.
  • -Patients with uncontrolled Type 1 or 2 diabetes mellitus.
  • -Patients with known uncontrolled thyroid disease.
  • -Patients with uncontrolled hypertension.
  • -Fasting triglycerides >350 mg/dL.
  • -Severe renal impairment (i.e., estimated glomerular filtration rate [eGFR] <30 mL/min/1.73m^2) at the screening visit.
  • -Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >2 x upper limit of normal (ULN).
  • -Creatine phosphokinase (CPK) >3 x ULN.

研究者

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