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临床试验/2023-509035-30-00
2023-509035-30-00已完成1 期

[HIBOU] : A phase I, single-center, randomized, double-blind, single-dose escalation, placebo-controlled clinical study to evaluate the safety, tolerability and pharmacokinetics of IMP21052 administered intravenously in three groups of healthy male and female volunteers

Direction Centrale Du Service De Sante Des Armees1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年1月2日最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
1

研究概览

简要总结

暂无简介。

入排标准

年龄范围
18 years 至 64 years(18-64 Years)
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Chef de bureau

Scientific

Direction Centrale Du Service De Sante Des Armees

研究点 (1)

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