EUCTR2017-004208-24-ES进行中（未招募）1 期
A randomized, double-blind, multicenter study to assess the safety, tolerability, and efficacy of a combination treatment of tropifexor (LJN452) and cenicriviroc (CVC) in adult patients with nonalcoholic steatohepatitis (NASH) and liver fibrosis (TANDEM)
ovartis Farmacéutica S.A.0 个研究点目标入组 200 人开始时间: 2018年7月30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
- 200
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
- •Written informed consent must be obtained before any assessment is
- •Male and female patients 18 years or older (at the time of the screening
- •visit). Patients must weigh at least 50 kg (110 lb) and no more than 200
- •kg (440 lb) to participate in the study.
- •Adequate liver biopsy sample for evaluation by a central reader.
- •Presence of NASH as demonstrated by histologic evidence based on liver
- •biopsy - NASH with fibrosis stage F2/F3, demonstrated on liver biopsy
- •with evaluation by central reading during the screening period.
- •Alternatively, a historical biopsy can be used if performed within 6
- •months prior to screening and evaluated by a central reader, if:
- •- the patient has been receiving any of the therapies listed in Table 5-4,
- •the dose must have been stable (since 1 month before the biopsy up to
- •and including screening)
- •- the patient's weight has been stable (maximum weight loss of 10%
- •since biopsy up to and including screening)
- •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 110
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 90
排除标准
- •Previous exposure to elafibranor, CVC, tropifexor, obeticholic acid
- •(OCA), LMB763 or any other FXR agonist.
- •Participated in a clinical trial and treated with any investigational
- •product being evaluated for the treatment of liver fibrosis or NASH in the
- •6 months before screening.
- •Patients taking medications prohibited by the protocol.
- •Current or history of significant alcohol consumption for a period of more
- •than 3 consecutive months within 1 year prior to screening (significant
- •alcohol consumption is defined as more than 20 g/day in females and
- •more than 30 g/day in males, on average) and/or a score on the
- •modified AUDIT questionnaire = 8
- •Uncontrolled diabetes defined as HbA1c = 9% at screening
- •Patients who are not candidates for liver biopsy
- •Presence of cirrhosis on liver biopsy or medical history
研究者
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