跳至主要内容
临床试验/EUCTR2016-000203-82-GB
EUCTR2016-000203-82-GB进行中(未招募)1 期

A Phase 2 Double-Blind, Randomized, Placebo-controlled, Dose-finding Study to Evaluate the Safety, Tolerability and Efficacy of Volixibat Potassium, an Apical Sodium-Dependent Bile Acid Transporter Inhibitor (ASBTi) in Adults with Nonalcoholic Steatohepatitis (NASH)

Shire Human Genetic Therapies, Inc.0 个研究点目标入组 197 人开始时间: 2016年5月27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
197

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

入选标准

  • 1. Age 18-80 years inclusive.
  • 2. Males and females
  • 3. Presence of = 5% steatosis on screening MRI from a centrally read radiologist performed either during the Screening period or within 6 months prior to the first visit.
  • 4. Histologic confirmation of NASH without cirrhosis (F0-F3) from a centrally read liver biopsy performed either during the Screening period or within 6 months prior to the first visit with a NAS of = 4 with a score of at least 1 in each component (steatosis, lobular inflammation, and hepatocyte ballooning).
  • 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 36
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1

排除标准

  • 1. Presence of or history of cirrhosis or evidence of decompensated liver disease (ie, ascites, variceal bleeding, etc.) or hepatocellular carcinoma.
  • 2. History or presence of other concomitant liver disease as assessed by the investigator or determined by laboratory findings
  • 3. Weight change = 5% after qualifying liver biopsy performed.
  • 4. Treatment with Vitamin E, thiazolidinediones, or glucagon-like peptide-1 receptors agonists (GLP1 RA) unless subject on a stable dose for 6 months prior to qualifying liver biopsy and not initiated after qualifying liver biopsy and will continue the same dosing regimen throughout study participation
  • 5. Uncontrolled diabetes defined as HbA1c of = 9.5% within 60 days prior to enrollment.
  • 6. Serum AST > 7 times upper limit of normal (ULN) at Screening.
  • 7. Serum ALT > 7 times ULN at Screening.
  • 8. Elevated serum creatinine = 2.0 mg/dL.
  • 9. International normalized ratio (INR) >1.3
  • 10. TB = 2.0 x ULN at Screening (Except for documented Gilbert’s syndrome]
  • 11. Platelet count < 130 × 10E9/L
  • 12. Uncontrolled thyroid disease.
  • 13. Type 1 diabetes mellitus.
  • 14. Known history of alcohol or other substance abuse within the last year or at any time during the study based on investigator’s discretion

研究者

相似试验

进行中(未招募)
1 期
A study to evaluate the saftey and efficacy of KZR-616 for the tretament of patients with active inflammations of the muscle and the skin (rheumatic disease)
EUCTR2019-002605-22-CZKezar Life Sciences, Inc.24
进行中(未招募)
1 期
Phase 2 Randomized, Double-blind, Placebo-controlled Study of the Effect of EDG-5506 on Biomarkers in Adults with Neuromuscular DiseaseBecker Muscular Dystrophy, McArdle Disease, Limb-Girdle Muscular DystrophyMedDRA version: 20.0Level: PTClassification code: 10059117Term: Becker's muscular dystrophy Class: 100000004850MedDRA version: 20.0Level: LLTClassification code: 10026970Term: McArdles disease Class: 10010331MedDRA version: 20.0Level: PTClassification code: 10028356Term: Muscular dystrophy Class: 100000004850
CTIS2022-500215-39-00Edgewise Therapeutics Inc.21
进行中(未招募)
1 期
A clinical trial to investigate the effects of MEDI9929, a drug used in clinical research, in adults with uncontrolled, severe asthma, a disease that causes variable and recurring inflammation of the airways leading to difficulty in breathing.Asthma
EUCTR2013-003269-33-HUMedImmune LLC(a wholly owned subsidiary of AstraZeneca PLC, One MedImmune Way, Gaithersburg, Maryland, 20878, USA )552
进行中(未招募)
1 期
A study to evaluate the safety and efficacy of KZR-616 for the tretament of patients with active inflammations of the muscle and the skin (rheumatic disease)Autoimmune Disorders Polymyositis and DermatomyositisMedDRA version: 20.0Level: HLGTClassification code 10003816Term: Autoimmune disordersSystem Organ Class: 10021428 - Immune system disorders
EUCTR2019-002605-22-DEKezar Life Sciences, Inc.24
进行中(未招募)
1 期
A clinical trial to investigate the effects of MEDI9929, a drug used in clinical research, in adults with uncontrolled, severe asthma, a disease that causes variable and recurring inflammation of the airways leading to difficulty in breathing.Asthma
EUCTR2013-003269-33-BGMedImmune LLC552