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
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
相似试验
已完成
2 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 controlsPrimary biliary cholangitissmall bile duct injury10019654fatty liver diseasenon-alcoholic steatohepatitisNL-OMON47216Academisch Medisch Centrum33
招募中
4 期
A randomized, open-label, positive drug parallel controlled clinical trial of Kesuting syrup in the treatment of COVID-19 (Light)COVID-19ITMCTR2200005986Shanghai Public Health Clinical Center
进行中(未招募)
不适用
An open-label, non-randomized pharmacokinetic and safety study of repeat doses of fluticasone furoate and GW642444M combination in healthy subjects and in subjects with severe renal impairmentHealthy subjects vs subjects with asthma or COPDMedDRA version: 12.1Level: LLTClassification code 10003553Term: AsthmaMedDRA version: 12.1Level: LLTClassification code 10010952Term: COPDEUCTR2010-020826-17-CZGlaxoSmithKline Research & Development Ltd18
尚未招募
4 期
Pharmacokinetics of twice or once daily DTG (50mg) in children with HIV and TBHIV/AIDSPaediatricsTuberculosisPACTR20200855470520220
进行中(未招募)
不适用
An open-label, non-randomized, pharmacokinetic and safety study of repeat doses of fluticasone furoate and GW642444M combination in healthy subjects and in subjects with mild, moderate or severe hepatic impairmenthealthy subjects and in subjects with mild, moderate or severe hepatic impairmentMedDRA version: 12.1Level: LLTClassification code 10052254Term: Hepatic impairmentEUCTR2010-020157-13-SKGlaxoSmithKline Research & Development Ltd36
