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临床试验/NCT04561466
NCT04561466已完成2 期

Study of Efficacy of Befizal® 200 mg for the Treatment of Leber Hereditary Optic Neuropathy

Hôpital Necker-Enfants Malades1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2019年3月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
14
试验地点
1
主要终点
Evolution of best corrected farsight visual acuity (in LogMAR)

研究概览

简要总结

Study of the efficiency of Béfizal® 200 mg in 14 adult patients with a LHON that occurred for less than 5 years. Patient must have certain specific mutations

详细描述

Study of the efficiency of Béfizal® 200 mg in 14 adult patients in whom the diagnosis of LHON obtained on anamnestic, clinical and ancillary testing / laboratory data. LHON should have occurred for less than 5 years and must be genetically proved with a 3460 or 11778 mitochondrial DNA mutation. Given the mode of transmission, genetic research may have been carried out in a maternal relative

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients in whom the diagnosis of LHON obtained on anamnestic, clinical and ancillary testing / laboratory data. LHON should have occurred for less than 5 years and must be genetically proved with a 3460 or 11778 mitochondrial DNA mutation. Given the mode of transmission, genetic research may have been carried out in a maternal relative

排除标准

  • * Any optic neuropathy for which the diagnosis of LHON is not formally confirmed or genetically proven;
  • LHON that started for more than 5 years;
  • LHON associated with another primary mutation than 3460 or 11778
  • Children or adult patients under guardianship or deprived of liberty by administrative or judicial decision;
  • Women of childbearing age ; pregnant or lactating women;
  • Patients who do not have affiliation to a social protection scheme (national or private insurance / beneficiary or assignee);
  • Patient who did not give its written, informed and signed consent;
  • Allergy to fibrate, bezafibrate and / or BEFIZAL® 200mg (Arrow Generiques) or one of these constituents;
  • Photosensitivity reactions related to fibrates;
  • Patient already receiving treatment with fibrates or HMG Co-A reductase inhibitors or anticoagulants;
  • Hepatic insuffisiency or dysfunction with increased of transaminases (AST and ALT) over 3 times of the normal;
  • Renal insufficiency with serum creatinine> 15 mg / L (> 135 mg / dL) Biliary pathology

研究组 & 干预措施

treatment group

Experimental

14 adult patients in whom the diagnosis of LHON obtained on anamnestic, clinical and ancillary testing / laboratory data. LHON should have occurred for less than 5 years and must be genetically proved with a 3460 or 11778 mitochondrial DNA mutation. Given the mode of transmission, genetic research may have been carried out in a maternal relative.

Befizal® 200 mg will be tested for one year

干预措施: Béfizal (Drug)

结局指标

主要结局

Evolution of best corrected farsight visual acuity (in LogMAR)

时间窗: Month12

Measurement of the best corrected farsight visual acuity by Early Treatment Diabetic Retinopathy Study type scale (range from -0.3 to 2.6) -0.3 is the best vision and 2.6 the worse

次要结局

  • Evolution of Farsight decimal best corrected visual acuity(Month 15)
  • Evolution of retinal nerve fibers layer Optical Coherent Tomography(Month 12)
  • Concentration of serum creatinine(Every three months until Month 15)
  • Rate of Partial thromboplastin time(Every three months until Month 15)
  • Farsight best corrected visual acuity(Month 3)
  • automated visual field(Month 9 of a treatment with BEFIZAL® 200mg (ARROW GENERIQUES) compare to Month 0)
  • Evolution of Farsight best corrected visual acuity(Month 3)
  • Evolution of Nearsight visual acuity(Month 15)
  • Concentration of Alanine aminotransférase(Every three months until Month 15)
  • automated visual field measurement(Month 15)
  • Concentration of lactate deshydrogenase(Every three months until Month 15)
  • Manual visual field measurement(Month 15)
  • National Eye Institute Visual Function Questionnaire 25(Month 12)
  • Concentration of high-density lipoprotein cholesterol(Every three months until Month 15)
  • Concentration of very low-density lipoprotein cholesterol(Every three months until Month 15)
  • Concentration of triglycerides(Every three months until Month 15)
  • Concentration of Aspartate aminotransférase(Every three months until Month 15)
  • Concentration of creatine kinase(Every three months until Month 15)

研究者

发起方
Hôpital Necker-Enfants Malades
申办方类型
Other
责任方
Principal Investigator
主要研究者

Christophe Orssaud

Principal investigator

Hôpital Necker-Enfants Malades

研究点 (1)

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