Pharmacokinetics Of Active And Passive Tetanus Immunization Given Concurrently In Subjects With No Known Primary Immunization History Or In Subjects With Tetanus Antibody Levels Below Protective Levels
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 6
- 试验地点
- 1
- 主要终点
- Antibody titer serum level at each time point
研究概览
简要总结
The goal of this study is to re-evaluate the tetanus antibody pharmacokinetic profile when Tetanus Immune Globulin (Human)(TIG) and Tetanus vaccine (Tetanus toxoid; TT) are given concurrently with strict control on the anatomical location and timing of administration of TIG and TT. Pharmacokinetic profile of antibody titer including the duration of adequate titer protection provided by TIG and TT given in combination will be assessed using a standardized administration regimen and standardized antibody assay procedure. This study may provide evidence for the recommendations of the World Health Organisation (WHO) whereby dual coverage with both a vaccine and tetanus hyperimmune would ideally provide the best coverage for anyone with the potential of developing tetanus.
详细描述
This is a prospective, open-label, single-center trial including a single group of subjects with no known primary immunization history with TT or >10 years have passed since the last dose of tetanus containing vaccine was received. The study will enroll six subjects who would receive both dT and TIG concurrently on Day 1.
All dosed subjects will be followed for 40 days during which Day 1, 2, 3, 4, 5, 7, 14, 21, 30 and 40 time levels of tetanus antibodies will be measured in order to determine the serum level vs. time curve, Cmax, Tmax, and duration of protective antibody levels.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age between 18 and 90 years.
- •Signed a written informed consent prior to initiation of any study-related procedures.
- •No known primary immunization history with TT/dT or >10 years have passed since the last dose of tetanus containing vaccine was received. Subjects with unknown or uncertain previous vaccination histories are considered to have no previous tetanus and toxoid doses. Subjects who have had military service since 1941 will be considered to have had 1 dose of tetanus vaccine.
- •Subjects must have documented tetanus antibody levels that are non-protective levels (< 0.15 IU/ml).
- •Subjects must be free of any presenting wound or wound infection
排除标准
- •History or suspicion of significant allergic reaction to intravenous immune globulin, and or blood products
- •A history of selective IgA deficiency (serum level <5.0 mg/dL) and known antibodies to IgA
- •Congestive heart failure (New York Association stage greater than Class II)
- •Conditions whose symptoms and effects could alter protein catabolism and/or IgG utilization (e.g. protein-losing enteropathies, nephrotic syndrome)
- •Women of child bearing potential who do not practice adequate contraception (i.e. chemical or mechanical methods) and pregnant or lactating females
- •Subjects who have severe thrombocytopenia or any coagulation disorder that would contraindicate intramuscular injections
- •TIG therapy within the previous six months
- •Investigational drug therapy within the previous three months
- •History of Thromboembolism
研究组 & 干预措施
Entered study
干预措施: Tetanus Immune Globulin (Human) (Drug)
Entered study
干预措施: Diphtheria-Tetanus Toxoids Adsorbed (Biological)
结局指标
主要结局
Antibody titer serum level at each time point
时间窗: 40 days
Cmax
时间窗: 40 days
Tmax
时间窗: 40 days
次要结局
未报告次要终点