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临床试验/NCT04885907
NCT04885907已完成4 期

A Randomised, Blinded, Controlled Trial of a Third Dose of Moderna COVID-19 Vaccine Versus Placebo in Solid Organ Transplant Recipients

University Health Network, Toronto4 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年5月25日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
120
试验地点
4
主要终点
anti-RBD antibody titer

研究概览

简要总结

This study will be a randomized, double-blind, placebo-controlled trial of a third dose of Moderna vaccine versus placebo. Participants will be those that have received two doses of mRNA-1273 COVID vaccine (Moderna) at 0 and 1 months. Participants will be randomized 1:1 to receive either a third dose of the mRNA-1273 vaccine or saline placebo at 3 months post initial vaccination.

详细描述

Solid organ transplant (SOT) recipients are at high risk of COVID-19 complications. The Moderna vaccine (mRNA-1273) has proven highly efficacious and safe in a phase III large, randomized controlled trial of 30,420 persons in the general population, and has been in use in Canada since December 2020. SOT patients show diminished response to mRNA vaccines in several studies with approximately 40-50% positive antibody after the second dose. In positive patients, antibody titers are lower than the general population and adverse events mirror the general population. The current study will recruit 120 SOT recipients who have received both scheduled doses of the Moderna vaccine at 0 and 1 months. The hypothesis is that a third dose of vaccine will significantly increase antibody titers. SOT participants will be recruited and randomized 1:1 to receive an additional dose of Moderna COVID-19 vaccine two months after the last dose vs saline placebo. The outcomes will measure anti-RBD antibody titer, T-cell immunity, local/systemic side effects, and rejection events.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Care Provider)

盲法说明

Participant and vaccinator will be blinded to vaccine vs placebo

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Solid organ transplant recipient who has previously received Moderna vaccine at 0 and 1 months
  • Able to provide informed consent

排除标准

  • Anaphylaxis or allergic reaction to Moderna vaccine

结局指标

主要结局

anti-RBD antibody titer

时间窗: 4-6 weeks after intervention

Percentage of patients that achieve anti-RBD of \>=100 U/mL in each arm

次要结局

  • Adverse events(7 days after intervention)
  • T-cell response(4-6 weeks after intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Deepali Kumar

Clinician-Investigator

University Health Network, Toronto

研究点 (4)

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