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临床试验/2024-518577-34-00
2024-518577-34-00招募中4 期

(A)nalysis of immunological (VA)riables in ex vivo (T)ofacitinib-treated human biopsies from (A)ctive ulcerative colitis patients to predict clinical (R)esponse (the AVATAR study).

Universita' Degli Studi Di Roma Tor Vergata2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年11月19日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
60
试验地点
2
主要终点
Immunological characterization

研究概览

简要总结

Research of predictive factors for response to Tofacitinib therapy in patients with ulcerative rectal colitis

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Provided written informed consent.
  • >18 years of age
  • Confirmed diagnosis of ulcerative colitis according to international guidelines (ECCO).
  • Patients with moderately-to-severely active disease, as defined as a Mayo score of 6-12, with a rectal bleeding subscore of 1 to
  • Endoscopic Mayo subscore of 2-
  • Patients who had failure or intolerant to at least one of the following agents: oral or intravenous glucocorticoids, azathioprine, 6-mercaptopurine, infliximab, golimumab or adalimumab.
  • Because the effects of Tofacitinib on pregnancy are not fully understood, women in childbearing age have to avoid pregnancy. Therefore the above cited patients have to use a suitable contraceptive method such as diaphragm, spiral or contraceptive pill before entering the study, for its entire duration and for 15 weeks after the suspension of the aforementioned drug

排除标准

  • Clinical findings suggestive of Crohn’s disease.
  • Ulcerative colitis limited to the distal 15 cm of colon.
  • Clinical signs of fulminant colitis, toxic megacolon, or indeterminate, microscopic, ischemic, or infectious colitis.
  • Patients at high risk of thromboembolism: 1) Patients with heart failure 2) Patients with inherited coagulation disorders 3) Patients who have history of venous thromboembolism, either deep venous thrombosis or pulmonary embolism. 4) Patients who use combined hormonal contraceptives or hormone replacement therapy. 5) Patients with malignancy 6) Patients undergoing major surgery
  • Known hypersensitivity/intolerance to tofacitinib (Xeljanz).
  • Presence of Child-Pugh class C hepatic impairment or eGFR<30 ml/min.
  • Chronic HIV, HBV, HCV infections (excluding patients with HCV infection treated with anti-viral agents in which serum HCV-RNA is not detectable).
  • Active TB or history of latent TB that has not been adequately treated, history of symptomatic herpes zoster (HZV) or any history of disseminated herpes simples (HSV) infections. Active opportunistic, clinically significant infections.
  • History of malignancy in the last 5 years.
  • Pregnant or lactating females.
  • Females of reproductive potential who are unwilling to abide by protocol specified contraceptive methods 8as defined by Appendix 1 in the Study protocol)

结局指标

主要结局

Immunological characterization

Immunological characterization

次要结局

未报告次要终点

研究者

申办方类型
Educational Institution
责任方
Principal Investigator
主要研究者

Massimo Claudio Fantini

Scientific

Universita' Degli Studi Di Roma Tor Vergata

研究点 (2)

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