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临床试验/EUCTR2016-002965-67-NL
EUCTR2016-002965-67-NL进行中(未招募)1 期

An open, non-randomized, parallel-group pharmokinetic and -dynamic, investigator-initiated study on effects of obeticholic acid (OCA) in bile of patients with primary biliary cholangitis (PBC) and non-alcoholic steatohepatitis (NASH) in comparison to healthy controls - OCABILE

AMC0 个研究点开始时间: 2017年3月29日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
AMC

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

  • -Male or female patients / volunteers of 18 to 75 years of age.
  • -Body mass index within 18 to 40 kg/m2
  • -Positive AMA (anti-mitochondrial antibody) testing (for PBC patients).
  • -Proven non-cirrhotic liver disease compatible with PBC stage I, II, III or NASH, no reliable signs of portal hypertension such as esophageal varices or ascites and/or pylephlebectasia > 15 mm, and a fibroscan < 15 kPa.
  • -The diagnosis of NASH must be confirmed by a liver biopsy (e.g. according Brunt criteria) in the last 24 months
  • 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 33
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Existing cardiac / hematological / renal / gastrointestinal diseases which might interfere with the drugs' safety, tolerability, absorption, pharmacokinetics and / or endoscopy.
  • -Other acute or chronic diseases which might affect absorption or metabolism of OCA
  • -Existing disorders of the coagulation system or treatment with anticoagulants or agents inhibiting thrombocyte aggregation
  • -Positive anti-HIV-test, HBsAg-test or anti-HCV-test.
  • -Acute inflammation of the gallbladder.
  • -Cholecystectomy
  • -Histologically proven cirrhotic liver disease or total bilirubin > 2 mg/dl or reliable signs of portal hypertension such as esophageal varices or ascites and/or pylephlebectasia > 15 mm and / or fibroscan > 15 kPa.

研究者

发起方
AMC

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