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临床试验/NL-OMON34913
NL-OMON34913已完成不适用

*A Phase I, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, pharmacokinetics and T-cell tolerizing effect of DC-TAB in healthy volunteers, after single and multiple dosing* - A phase I trial with DC-TAB

Delta Crystallon BV0 个研究点目标入组 76 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
已完成
入组人数
76

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

年龄范围
18 至 99(—)

入选标准

  • you have given your written consent to take part in this study;
  • you are between 18 and 55 years of age (inclusive);
  • you are in good physical and mental health;
  • your body weight must be appropriate in relation to your height;
  • The use of suitable anti conception in the 3 months before start of the study and you will remain using this until 3 months after the study and/or you can not invoke an pregnancy (males) or you can not get pregnant (females)
  • no abnormalities are diagnosed during the screening.

排除标准

  • If you are pregnant, planning to get pregnant or breastfeeding;
  • If you have relatives (1st degree) who have MS;
  • If you smoke 5 or more cigarettes per day or are not able to stop smoking during the admission period;
  • If you have abused drug (past and present) and or alcohol
  • The use of prescribed medication in the 14 days before start of the study, except for hormone based anticonceptionals, standard vitamines and paracetamol;
  • If you recieved a vaccination within the 4 weeks before the start of the study;
  • you have taken part in another clinical drug study during the last 3 months prior to the study;
  • you have donated blood in the three months before admission;
  • you have donated plasma in the 7 days before admission;
  • if you have recieved bloodproducts in the 6 month before start of start of the study;
  • you are Hepatitis B, C or HIV positive;
  • If no immune response can be achieved by DC-TAB in your blood;
  • you are not suitable to participate in this study according to the investigator.

研究者

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