此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Typhoid Conjugate Vaccine Introduction in Madagascar (TyMA): Evaluation of the Real-World Effectiveness of the Vi-CRM197 Typhoid Conjugate Vaccine in Madagascar (TyMA)

2026年11月5日 更新者:Rita Soares Barbosa Cardona

This study evaluates the real-world effectiveness, safety, and immunogenicity of a single dose of the Vi-CRM197 typhoid conjugate vaccine (TCV) delivered through a mass vaccination campaign in selected districts of Madagascar. The study targets individuals aged 9 months to 45 years living in defined catchment areas with a high burden of typhoid fever.

The project integrates three components: a population census with geographic mapping, a vaccination campaign using a WHO-prequalified Vi-CRM197 TCV, and prospective surveillance for typhoid fever. Vaccine effectiveness will be assessed by comparing the incidence of blood culture-confirmed Salmonella Typhi infection among vaccinated and unvaccinated individuals during follow-up. Additional outcomes include clinically suspected typhoid fever, severe disease, vaccine safety, immunogenicity, antibiotic use and consumption, and carriage of antimicrobial resistance (AMR) markers.

The study aims to generate real-world evidence to inform public health decision-making regarding typhoid vaccine introduction and its broader impact on disease burden and antimicrobial resistance in endemic settings.

研究概览

详细说明

Typhoid fever, caused by Salmonella enterica serovar Typhi, remains a major public health problem in many low- and middle-income countries, particularly in settings with limited access to safe water and sanitation. The emergence of antimicrobial resistance further complicates treatment and underscores the importance of preventive strategies such as vaccination. Typhoid conjugate vaccines (TCVs) have demonstrated efficacy in clinical trials, but data on their real-world effectiveness and broader population impact in African settings remain limited.

The TyMA study evaluates the impact of a mass vaccination campaign using a WHO-prequalified Vi-CRM197 TCV in selected districts of Madagascar. The study employs a population-based design integrating a baseline census, vaccination activities, and longitudinal surveillance.

Eligible individuals aged 9 months to 45 years will receive a single intramuscular dose of Vi-CRM197 during a community vaccination campaign.

Vaccine effectiveness will be assessed through both active and enhanced facility-based surveillance for typhoid fever over approximately three years Blood culture testing will be performed for suspected cases to identify laboratory-confirmed S. Typhi infection. Effectiveness estimates will be derived by comparing incidence rates between vaccinated individuals and unvaccinated controls within the censused population.

Subgroups of participants will be enrolled in additional cohorts to evaluate specific outcomes:

  • Safety cohort: Active monitoring for adverse events following vaccination
  • Immunogenicity cohort: Measurement of anti-Vi IgG antibody responses over time
  • Active follow-up subpopulation: Regular household visits to identify febrile illness and healthcare utilization
  • AMR cohort: Assessment of antimicrobial use, consumption, and carriage of antimicrobial resistance markers

Passive surveillance in selected healthcare facilities will complement active follow-up to capture cases presenting for care. Data on antibiotic prescribing, hospitalization, and clinical outcomes will also be collected.

The study will assess direct, indirect, and overall vaccine protection at the population level and explore the impact of vaccination on antimicrobial use and resistance patterns. Findings are expected to provide critical evidence to support national and regional policy decisions regarding typhoid vaccine introduction and strategies to mitigate antimicrobial resistance.

研究类型

介入性

注册 (估计的)

60000

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Florian Marks
  • 电话号码:+82 10-8703-3813
  • 邮箱:fmarks@ivi.int

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

9个月 至 45年 (孩子、成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age 9 months to 45 years at the time of vaccination
  • Resident of the defined study catchment area in Madagascar
  • Parent(s), legal guardian, or participant (if adult) able and willing to provide written informed consent (and assent where applicable)
  • Willing to comply with study procedures and follow-up for the duration of the study

Exclusion Criteria:

  • Any medical or social condition that, in the opinion of the investigator, would interfere with participation or study procedures
  • Known allergy or hypersensitivity to any component of the Vi-CRM197 typhoid conjugate vaccine
  • Parent(s), legal guardian, or participant unwilling or unable to provide informed consent/assent

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Vaccination Campaign: Vi-CRM197 Typhoid Conjugate Vaccine

Participants aged 9 months to 45 years residing in the defined catchment area will be offered a single intramuscular dose of the Vi-CRM197 typhoid conjugate vaccine as part of a population-based vaccination campaign. Vaccine effectiveness will be evaluated prospectively through active and facility-based surveillance for typhoid fever.

Single-dose Vi-CRM197 typhoid conjugate vaccine administered intramuscularly to age-eligible individuals during a mass vaccination campaign. The vaccine is WHO-prequalified and intended to prevent infection with Salmonella enterica serovar Typhi.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Incidence of blood culture-confirmed typhoid fever (Salmonella Typhi)
大体时间:From census enrollment up to 52 months

Incidence of typhoid fever defined as isolation of Salmonella enterica serovar Typhi from blood culture among individuals residing in the study catchment area. Vaccine effectiveness will be estimated by comparing incidence between individuals who received a single dose of Vi-CRM197 typhoid conjugate vaccine during the vaccination campaign and unvaccinated individuals within the censused population using active and enhanced facility-based surveillance.

From census enrollment up to 52 months

次要结果测量

结果测量
措施说明
大体时间
Incidence of clinically suspected typhoid fever
大体时间:From census enrollment up to 52 months

Incidence of clinically suspected typhoid fever among residents of the study catchment area identified through active household surveillance and enhanced facility-based surveillance, regardless of laboratory confirmation. Comparisons will be made between vaccinated and unvaccinated individuals.

From census enrollment up to 52 months
Incidence of severe typhoid fever
大体时间:From census enrollment up to 52 months

Incidence of severe typhoid fever, including cases requiring hospitalization or presenting with severe complications, among vaccinated and unvaccinated individuals in the study population

From census enrollment up to 52 months
Solicited and unsolicited adverse events following vaccination
大体时间:Solicited adverse events: Days 0-7 post-vaccination of a subset of participants; Unsolicited adverse evetns : up to 28 days pos vaccination. Aerious adverse events: From vaccination enrollment up to 52 months

Occurrence of solicited local and systemic adverse events within 7 days after vaccination and unsolicited adverse events and serious adverse events during follow-up among participants receiving the Vi-CRM197 vaccine.

Solicited adverse events: Days 0-7 post-vaccination of a subset of participants; Unsolicited adverse evetns : up to 28 days pos vaccination. Aerious adverse events: From vaccination enrollment up to 52 months
Anti-Vi IgG antibody response following vaccination
大体时间:Baseline to 24 months post-vaccination

Immunogenicity assessed by seroconversion (≥4-fold rise in anti-Vi IgG titers from baseline) and geometric mean titers measured in a subset of vaccinated participants at predefined time points after vaccination.

Baseline to 24 months post-vaccination
Carriage of antimicrobial resistance markers
大体时间:Baseline to 12 months

Prevalence and changes in antimicrobial resistance markers in gastrointestinal and respiratory samples among vaccinated and unvaccinated individuals in a subset cohort.

Baseline to 12 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2023年7月23日

初级完成 (估计的)

2026年12月1日

研究完成 (估计的)

2027年6月1日

研究注册日期

首次提交

2026年11月2日

首先提交符合 QC 标准的

2026年11月5日

首次发布 (实际的)

2026年11月12日

研究记录更新

最后更新发布 (实际的)

2026年11月12日

上次提交的符合 QC 标准的更新

2026年11月5日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅