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临床试验/jRCT2031260334
jRCT2031260334招募中不适用

A phase 3 randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of secutrelvir in participants with COVID-19 (COVID-19)

未提供0 个研究点目标入组 1,200 人开始时间: 待定
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,200

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

入排标准

年龄范围
12age old over 至 75age old not(—)
性别
All

入选标准

  • Must be 12 to < 18 years of age with a body weight >= 40 kg, or >= 18 and < 75 years of age regardless of body weight.
  • Must have >= 1 of the following COVID-19 symptoms, present within 24 hours prior to randomization.
  • Confirmed SARS-CoV-2 infection as determined by any SARS-CoV-2 test from any respiratory tract specimen, collected <= 48 hours prior to randomization.
  • Must be randomized within 48 hours of COVID-19 symptom onset.

排除标准

  • Documented respiratory infection (eg, influenza, respiratory syncytial virus infection) other than COVID-19 within 14 days prior to the screening visit.
  • Known history of cirrhosis or liver decompensation (including ascites, variceal bleeding, or hepatic encephalopathy).
  • Suspected or confirmed COVID-19 outside of the current episode within 3 months of randomization.

研究者

发起方
未提供

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