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临床试验/RPCEC00000393
RPCEC00000393尚未招募2 期

Evaluation of the effect and safety terapeutic of Jusvinza in severe patients with COVID-19

Center for Genetic Engineering and Biotechnology (CIGB), Havana0 个研究点目标入组 108 人开始时间: 2021年10月26日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
108

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. Masking: Open. Control group: Active. Assignment: Parallel. Purpose: Treatment

入排标准

年龄范围
19 years 至 one(—)
性别
All

入选标准

  • 1. Age = 19.
  • 2. Virologial diagnosis by RT-PCR to SARS-Cov-2.
  • 3. Patients with serious status.
  • 4. Willingness of the patient through informed consent

排除标准

  • 1. Patients with kidney disease on hemodialysis.
  • 2. Known hypersensitivity to any of the components of the formulations under study
  • 3. Pregnancy or breastfeeding.

研究者

发起方
Center for Genetic Engineering and Biotechnology (CIGB), Havana

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