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临床试验/EUCTR2006-006319-54-GB
EUCTR2006-006319-54-GB进行中(未招募)1 期

An Open Label Evaluation of the Safety and Efficacy of Basiliximab Maintenance in Ulcerative Colitis - BSX-002

Cerimon Pharmaceuticals, Inc.0 个研究点目标入组 135 人开始时间: 2006年12月7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
135

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

  • Subjects must satisfy all of the following inclusion criteria to be eligible for the study:
  • 1.Previously met eligibility criteria in the previous basiliximab UC study
  • 2.Completed all study visits in previous study, even if they discontinued study drug dosing before the end of the study
  • 3.Must have a total Mayo score at entry to BSX-002 consistent with clinical response or clinical remission as follows:
  • -Clinical remission is defined as a total Mayo score of 2 points or less, with no individual subscore exceeding 1 point.
  • -Clinical response is defined as a decrease in total Mayo score of at least 3 points, with a decrease in rectal bleeding subscore of at least 1 point and/or an absolute rectal bleeding subscore of 0 or 1.
  • 4. Signed a current IRB/IEC-approved informed consent form
  • 5.Females of childbearing potential must use an effective birth control method, and be willing to continue birth control during the study, and for 4 months after the last dose of study drug.
  • 6.Females of non-childbearing potential should be surgically sterile (bilateral tubal ligation with surgery at least 6 months before study entry, hysterectomy, or bilateral oophorectomy at least 2 months before study entry) or post-menopausal for at least 2 years.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Presence of any of the following conditions will exclude the subject from eligibility for the study:
  • 1.Subject discontinued blinded study drug in previous study due to a study-drug related adverse event
  • 2.Subject is severely ill, as evidenced by more than 6 episodes of loose stools, all of them bloody, during a 24-hour period within the prior 7 days, concurrent with any of the following systemic features:
  • -Heart rate > 90 beats/min at rest
  • -Temperature > 37.8 degrees C
  • -Hemoglobin < 10.5 g/dL
  • 3. Subject is currently receiving a restricted/prohibited concomitant medication
  • 4.Subject has undergone colectomy (total, or subtotal)
  • 5.Subject is pregnant or breast-feeding
  • 6.Prior noncompliance with previous study visit schedule and requirements

研究者

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