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临床试验/EUCTR2014-003164-21-BE
EUCTR2014-003164-21-BE进行中(未招募)1 期

Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects with Liver Fibrosis - CENTAUR

Tobira Therapeutics, Inc., a subsidiary of Allergan plc0 个研究点目标入组 289 人开始时间: 2014年10月2日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
289

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

  • --Histological evidence of NASH, based on Screening biopsy, with a NAS of = 4 with at least 1 in each component of NAS
  • --Histological evidence of liver fibrosis defined as NASH CRN System Stage 1 to 3, inclusive, based on Screening biopsy
  • --Meeting any of the 3 following major criteria (a, b, c):
  • a. Documented evidence of type 2 diabetes mellitus (T2DM)
  • b. High BMI (> 25 kg/m2) with at least 1 of the following criteria of the metabolic syndrome, as defined by the NCEP:
  • i. Central obesity: waist circumference = 102 cm or 40 inches (male), = 88 cm or 35 inches (female)
  • ii. Dyslipidemia: TG = 1.7 mmol/L (150 mg/dL)
  • iii. Dyslipidemia: HDL-cholesterol < 40 mg/dL (male), < 50 mg/dL (female)
  • iv. Blood pressure = 130/85 mmHg (or treated for hypertension)
  • v. Fasting plasma glucose = 6.1 mmol/L (110 mg/dL)
  • c. Bridging fibrosis (NASH CRN Stage 3) and/or definite NASH (NAS = 5)
  • --Agree to have one liver biopsy at Screening, one at Year 1, and one at the end
  • of study treatment (Year 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 226
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 26

排除标准

  • --Hepatitis B surface antigen (HBsAg) positive
  • --Hepatitis C antibody (HCVAb) positive with the following 2 exceptions:
  • a. Subjects previously treated for viral hepatitis C with at least a 1-year period since documented sustained virologic response at Week 12 (post-treatment) may be eligible if all other eligibility criteria are met
  • b. Subjects with presence of hepatitis C antibody but negative hepatitis C virus RNA without treatment (i.e., spontaneous clearance) may be eligible if all other eligibility criteria are met
  • --Prior or planned liver transplantation
  • --Other known causes of chronic liver disease, including alcoholic liver disease
  • --History of cirrhosis and/or hepatic decompensation including ascites, hepatic encephalopathy or variceal bleeding
  • --Alcohol consumption greater than 21 units/week for males or 14 units/week for females (one unit of alcohol is ½ pint of beer [285 mL], 1 glass of spirits
  • [25 mL] or 1 glass of wine [125 mL])

研究者

发起方
Tobira Therapeutics, Inc., a subsidiary of Allergan plc

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