跳至主要内容
临床试验/EUCTR2014-003942-28-BE
EUCTR2014-003942-28-BE进行中(未招募)1 期

Randomized, Global, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Vedolizumab IV for the Treatment of Primary Sclerosing Cholangitis, With Underlying Inflammatory Bowel Disease

Takeda Development Centre Europe, Ltd.0 个研究点目标入组 258 人开始时间: 2016年3月10日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
258

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

  • 1. In the opinion of the investigator, the subject is capable of understanding and complying with protocol requirements.
  • 2. The subject or, when applicable, the subject’s legally acceptable representative signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures.
  • 3. The subject has chronic cholestatic liver disease, of at least 6 months duration, with a subsequent diagnosis of PSC, based on cholangiographic findings of intrahepatic and/or extrahepatic bile duct irregularities consistent with PSC.
  • 4. The subject has a diagnosis of IBD (either UC, CD, or IBDU), established at least 3 months prior to enrollment by clinical and endoscopic evidence and corroborated by a histopathology report.
  • 5. The subject is male or female and aged 18 years and older, inclusive.
  • 6. A male subject who is non-sterilized and sexually active with a female partner of childbearing potential agrees to use adequate contraception from signing of the informed consent throughout the duration of the study and for 18 weeks after last dose.
  • 7. A female subject of childbearing potential* who is sexually active with a non-sterilized male partner agrees to routinely use adequate contraception from signing of the informed consent throughout the duration of the study and for 18 weeks after the last dose.
  • 8. The subject has had a colorectal cancer screen within 12 months of the Screening Visit with no signs of malignancy, dysplasia, or neoplasia.
  • 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 246
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 12

排除标准

  • 1. The subject has had previous exposure to vedolizumab
  • 2. The subject has a history of hypersensitivity or allergies to vedolizumab
  • 3. The subject has had previous exposure to natalizumab, efalizumab, rituximab or any other integrin antagonist
  • 4. The subject has received any investigational or approved biologic or biosimilar agent
  • 5. The subject has received any of the following for the treatment of underlying disease within 30 days of screening:
  • Nonbiologic therapies other than those specifically listed in the protocol Section 7.3.1 Permitted Medications for the Treatment of IBD
  • An approved nonbiologic therapy in an investigational protocol
  • 6. The subject has, in the judgment of the investigator, clinically significant abnormal hematological parameters of hemoglobin, hematocrit, or erythrocytes
  • 7. The subject has any history of malignancy, except for (a) adequately treated nonmetastatic basal cell skin cancer; (b) squamous cell skin cancer that has not recurred for at least 1 year prior to randomization; and (c) history of cervical carcinoma in situ that has not recurred for at least 3 years prior to randomization
  • 8. The subject has a history of any major neurological disorders, including stroke, multiple sclerosis, brain tumor, demylelinating or neurodegenerative disease
  • 9. The subject has a positive response on the PML subjective symptom checklist prior to the administration of study drug

研究者

相似试验

进行中(未招募)
1 期
Efficacy and Safety of Vedolizumab IV in the treatment of PrimarySclerosing Cholangitis in patients with Inflammatory Bowel DiseasePrimary Sclerosing Cholangitis (PSC)Inflammatory Bowel Disease (IBD)MedDRA version: 18.1Level: LLTClassification code 10036732Term: Primary sclerosing cholangitisSystem Organ Class: 100000004871MedDRA version: 18.1Level: PTClassification code 10021972Term: Inflammatory bowel diseaseSystem Organ Class: 10017947 - Gastrointestinal disordersMedDRA version: 18.1Level: LLTClassification code 10021973Term: Inflammatory bowel disease NOSSystem Organ Class: 10017947 - Gastrointestinal disorders
EUCTR2014-003942-28-DETakeda Development Centre Europe, Ltd.258
进行中(未招募)
1 期
Efficacy and Safety of Vedolizumab IV in the treatment of PrimarySclerosing Cholangitis in patients with Inflammatory Bowel DiseasePrimary Sclerosing Cholangitis (PSC)Inflammatory Bowel Disease (IBD)MedDRA version: 19.0Level: LLTClassification code 10036732Term: Primary sclerosing cholangitisSystem Organ Class: 100000004871MedDRA version: 19.0Level: PTClassification code 10021972Term: Inflammatory bowel diseaseSystem Organ Class: 10017947 - Gastrointestinal disordersMedDRA version: 19.0Level: LLTClassification code 10021973Term: Inflammatory bowel disease NOSSystem Organ Class: 10017947 - Gastrointestinal disorders
EUCTR2014-003942-28-FRTakeda Development Centre Europe, Ltd.99,999
进行中(未招募)
1 期
Efficacy and Safety of Vedolizumab IV in the treatment of PrimarySclerosing Cholangitis in patients with Inflammatory Bowel DiseasePrimary Sclerosing Cholangitis (PSC)Inflammatory Bowel Disease (IBD)MedDRA version: 18.1Level: LLTClassification code 10036732Term: Primary sclerosing cholangitisSystem Organ Class: 100000004871MedDRA version: 18.1Level: PTClassification code 10021972Term: Inflammatory bowel diseaseSystem Organ Class: 10017947 - Gastrointestinal disordersMedDRA version: 18.1Level: LLTClassification code 10021973Term: Inflammatory bowel disease NOSSystem Organ Class: 10017947 - Gastrointestinal disorders
EUCTR2014-003942-28-SETakeda Development Centre Europe, Ltd.258
进行中(未招募)
1 期
Efficacy and Safety of Vedolizumab IV in the treatment of PrimarySclerosing Cholangitis in patients with Inflammatory Bowel DiseasePrimary Sclerosing Cholangitis (PSC)Inflammatory Bowel Disease (IBD)MedDRA version: 18.1Level: LLTClassification code 10036732Term: Primary sclerosing cholangitisSystem Organ Class: 100000004871MedDRA version: 18.1Level: PTClassification code 10021972Term: Inflammatory bowel diseaseSystem Organ Class: 10017947 - Gastrointestinal disordersMedDRA version: 18.1Level: LLTClassification code 10021973Term: Inflammatory bowel disease NOSSystem Organ Class: 10017947 - Gastrointestinal disorders
EUCTR2014-003942-28-ATTakeda Development Centre Europe, Ltd.258
进行中(未招募)
1 期
Efficacy and Safety of Vedolizumab IV in the treatment of PrimarySclerosing Cholangitis in patients with Inflammatory Bowel Disease
EUCTR2014-003942-28-PLTakeda Development Centre Europe, Ltd.258