跳至主要内容
临床试验/jRCT2071230085
jRCT2071230085招募中不适用

Phase I Study of AK1910 in Healthy Japanese Subjects, Healthy Caucasian Subjects, Patients with Systemic Lupus Erythematosus (Single Dose and Multiple Dose Study)

Asahi Kasei Pharma Corporation0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
120
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
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Double Blind

入排标准

年龄范围
18age old over 至 75age old not(—)
性别
All

入选标准

  • [1] Japanese healthy men and women or Caucasian healthy men
  • [2] Individuals >=18 to <45 years of age at the time of informed consent
  • [3] Individuals who fully understand the details of the study and who are capable of providing written informed consent
  • [1] Patients who meet the EULAR/ACR 2019 SLE classification criteria and have a diagnosis of SLE
  • [2] Individuals >=18 years to < 75 years at the time of informed consent
  • [3] Individuals who fully understand the details of the study and who are capable of providing written informed consent

排除标准

  • [1] Past history of disease in organsystems considered unsuitable for this study
  • [2] Past history of allergy or anaphylaxis to drugs or other substances
  • [3] Other protocol defined exclusion criteria could apply
  • [1] Patients with active central nervouslupus or systemic autoimmune diseases other than systemic lupus erythematosus
  • [2] Patients with history or complications of serious diseases considered unsuitable for this study
  • [3] Patients with history or complications of infections that may affect safety and efficacy evaluation

结局指标

主要结局

-

*Plasma concentration of compound(s) *Number of participants with adverse events

次要结局

未报告次要终点

研究者

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