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临床试验/EUCTR2019-002324-32-SK
EUCTR2019-002324-32-SK进行中(未招募)1 期

A randomized, double-blind, parallel-group, multicenter study to assess efficacy, safety, and tolerability of oral tropifexor (LJN452) & licogliflozin (LIK066) combination therapy and each monotherapy, compared with placebo for treatment of adult participants with nonalcoholic steatohepatitis (NASH) and liver fibrosis (ELIVATE)

ovartis Pharma AG0 个研究点目标入组 380 人开始时间: 2020年12月28日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
380

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

  • Presence of NASH with fibrosis as confirmed by central reader's evaluation of liver biopsy obtained no more than 6 months before randomization. demonstrated by the following:
  • - NASH using NAFLD Activity Score (NAS) >= 4 with at least 1 point each in inflammation and ballooning
  • - Fibrosis stage 2 or 3 using NASH CRN fibrosis criteria
  • 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 325
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 55

排除标准

  • Type 1 diabetes mellitus
  • Uncontrolled type 2 diabetes defined as glycated hemoglobin (HbA1c) = 9% at screening
  • HbA1c < 6.5% at screening in Type 2 diabetics currently treated with insulin or sulfonylureas
  • Clinical evidence of liver impairment as defined by the presence of any of the following abnormalities:
  • ?Abnormal platelet count
  • ?Serum albumin < LLN (see central lab manual)
  • ?International Normalized Radio (INR) > ULN
  • ?ALT or AST > 5xULN (in either of the 2 values)
  • ?Total bilirubin > ULN (see central lab manual) (including Gilbert's syndrome)
  • ?Alkaline phosphatase > 300 IU/L (in either of the 2 values during screening)
  • ?History of esophageal varices, ascites or hepatic encephalopathy
  • ?Splenomegaly

研究者

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