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临床试验/NCT01063140
NCT01063140已完成不适用

Rabies Immune Plasma Booster Program - A Clinical Study Conducted as an Investigational New Drug Study

CSL Behring1 个研究点 分布在 1 个国家目标入组 491 人开始时间: 2009年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
CSL Behring
入组人数
491
试验地点
1
主要终点
Geometric mean titer (GMT) for rabies plasma donations received after booster injections

研究概览

简要总结

Rabies immune globulin is a product that is lifesaving to unvaccinated individuals exposed to the rabies virus. Rabies immune globulin is made from plasma from immune donors. Currently the only practical method to obtain this plasma is to immunize normal volunteer Source Plasma donors and collect their plasma while titers are adequate. The use of rabies vaccine for immunization of normal Source Plasma donors is currently limited to a level that, while protective for the individual, is unsuitable for production of rabies immune globulin.

The objective of this study is to obtain efficacy and safety data regarding the rabies boostering program to demonstrate that:

  1. Rabies immune plasma production can be substantially increased by giving booster doses to previously immunized donors whose titers are below 10.0 IU/mL.
  2. It is safe for normal Source Plasma donors to receive booster doses of rabies vaccine on a regular basis.

This study utilizes two rabies vaccines approved by the FDA, Imovax® (Sanofi-Pasteur) and RabAvert® (Novartis).

研究设计

研究类型
Observational
时间视角
Prospective

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

  • Meet requirements for Source Plasma donors
  • Completed initial series of rabies antibody injections with no serious adverse events for at least 90 days prior to enrollment
  • Compliance with program requirements
  • Signed informed consent

排除标准

  • Failure to meet requirements to be Source Plasma donor
  • Non-compliance with the program
  • Experience a serious adverse reaction

结局指标

主要结局

Geometric mean titer (GMT) for rabies plasma donations received after booster injections

时间窗: 30-day intervals for the duration of the study (up to 2 years)

次要结局

  • Adverse Event Reaction Rate(30-35 days after each injection)

研究者

发起方
CSL Behring
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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