跳至主要内容
临床试验/jRCT2031210637
jRCT2031210637已完成不适用

An Open-label, Multi-center Extension Study to Evaluate the Long-term Safety and Efficacy of Deucravacitinib in Participants with Moderate to Severe Crohn's Disease or Moderate to Severe Ulcerative Colitis

Bristol-Myers Squibb0 个研究点目标入组 15 人开始时间: 2022年3月22日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
15
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • Previously completed OLE treatment in 1 of the parent CD or UC studies

排除标准

  • Any disease or medical condition that, in the opinion of the investigator, would make the participant unsuitable for this study, would interfere with the interpretation of participant safety or study results, or is considered unsuitable by the investigator for any other reason.

结局指标

主要结局

-

To assess the safety and tolerability of long-term use of BMS-986165(Deucravacitinib)

次要结局

未报告次要终点

研究者

发起方
Bristol-Myers Squibb

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