跳至主要内容
临床试验/EUCTR2020-005513-41-FR
EUCTR2020-005513-41-FR进行中(未招募)1 期

An open-label extension trial to evaluate the long-term safety of apraglutide in short bowel syndrome

VectivBio AG0 个研究点目标入组 154 人开始时间: 2021年5月21日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
VectivBio AG
入组人数
154

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Males and females with a diagnosis of SBS-IF secondary to surgical resection of the small intestine, with CIC or stoma, who have completed parent trials TA799-007 or TA799-013 and:
  • a. Did not meet any stopping criteria.
  • b. Received a minimum of 70% of the planned doses in the trial (unless an AE precluded the subject from meeting this percentage; in this case, the Investigator will decide if the subject will benefit from enrolling in the trial).
  • c. Complete the last two scheduled visits of the parent trial. Subjects who were forced to withdraw from TA799-007 for logistical reasons not related to the efficacy or safety of apraglutide (e.g., hospitalization for a car accident, COVID-19 pandemic, or emergency surgery) which resulted in several consecutive missed doses may be eligible to participate in this trial upon approval by the Medical Monitor.
  • 2. Able to give informed consent and agree to follow the details of participation as outlined in this protocol.
  • 3. Women of childbearing potential must agree to use a highly effective method of contraception during the trial and for 4 weeks after the end of trial (EOT) visit.
  • 4. Male subjects with a female partner of childbearing potential must commit to practice methods of contraception and abstain from sperm donation during the trial and for 2 weeks after the EOT Visit.
  • 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 76
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 62

排除标准

  • 1. Subject not capable of understanding or not willing to adhere to the trial visit schedules and other protocol requirements.
  • 2. Any other reason judged not eligible by the Investigator.

研究者

发起方
VectivBio AG

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