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临床试验/ACTRN12616001657415
ACTRN12616001657415招募中1 期

A Phase 1, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability and pharmacokinetics (PK) of escalating single dose of brincidofovir administered intravenously in healthy adult subjects

Chimerix, Inc0 个研究点目标入组 40 人开始时间: 2016年12月1日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
Chimerix, Inc
入组人数
40

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
Randomised controlled trial
主要目的
Treatment

入排标准

年龄范围
18 Years 至 55 Years(—)
性别
All

入选标准

  • non-child bearing potential
  • willing and able to provide written informed consent
  • non-tobacco/non-nicotine user in the past 6 months
  • body weight no greater than 50kg
  • BMI from 18-32 kg/m
  • no significant medical history
  • males cannot donate sperm during participation

排除标准

  • child bearing potential
  • investigational drug or clinical study in the past 30 days
  • had any infection within the past 2 weeks
  • history of history chronic liver disease

研究者

发起方
Chimerix, Inc

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