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A Study on the Immune Response and Safety of a Combined Vaccine Against Diphtheria, Tetanus and Acellular Pertussis (dTpa) in Healthy Japanese Adolescents Aged 11 Years to <13 Years

2026年9月7日 更新者:GlaxoSmithKline

A Phase 3, Non-randomized, Single-arm, Open-label Study to Assess the Immunogenicity, Safety and Reactogenicity of Combined Reduced-antigen-content Diphtheria, Tetanus and Acellular Pertussis (dTpa) Vaccine, Administered as a Booster Dose in Healthy Japanese Adolescents Aged 11 Years to <13 Years

The purpose of the study is to assess the immune response, reactogenicity and safety of a booster dose of dTpa vaccine 1 month after vaccination in healthy Japanese participants aged 11 to <13 years.

研究概览

研究类型

介入性

注册 (实际的)

90

阶段

  • 第三阶段

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。

学习地点

      • Fukuoka、日本、812-0871
        • GSK Investigational Site
      • Hokkaido、日本、004-0052
        • GSK Investigational Site
      • Hokkaido、日本、006-0814
        • GSK Investigational Site
      • Hokkaido、日本、062-0907
        • GSK Investigational Site
      • Kumamoto、日本、862-0924
        • GSK Investigational Site
      • Mie、日本、511-0865
        • GSK Investigational Site
      • Osaka、日本、554-0014
        • GSK Investigational Site
      • Saitama、日本、360-0812
        • GSK Investigational Site
      • Saitama、日本、337-0042
        • GSK Investigational Site
      • Shizuoka、日本、420-8623
        • GSK Investigational Site

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

  • 孩子

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Participants and/or participants' parent(s)/ Legally acceptable representative(s) [LAR(s)], who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
  • Physical or digital informed assent obtained from the participant prior to performance of any study-specific procedure.
  • Physical or digital informed consent obtained from the parent(s)/LAR(s) of the participant prior to performance of any study-specific procedure.
  • Healthy participants as established by medical history and clinical examination at screening.
  • Male/female participant between and including 11 and <13 years of age at the time of the study intervention administration (Visit 1/Day 1).
  • Previously completed all routine childhood vaccinations to the best knowledge of the participant's parent(s)/LAR(s). Participants with documented previous diphtheria, tetanus and pertussis vaccination (primary series and first booster) as per routine vaccination in Japan prior to study enrolment.
  • Participants did not receive an additional diphtheria, tetanus with or without pertussis vaccination within 5 years prior to enrolment in the study.
  • Japanese ethnic origin.
  • Participants of non-childbearing potential may be enrolled in the clinical study.
  • Participant of childbearing potential may be enrolled in the study if the participant:
  • has practiced adequate contraception for at least 30 days prior to study intervention administration, and
  • has a negative pregnancy test within 24 hours prior to the study intervention administration, and
  • has agreed to continue adequate contraception during the entire treatment period and for 8 weeks after completion of the study intervention administration series.

Exclusion Criteria:

Medical conditions

  • History of physician-diagnosed or laboratory-confirmed diphtheria, tetanus or pertussis diseases within the past 5 years.
  • History of encephalopathy after administration of a previous dose of pertussis vaccine that could not be attributed to another identifiable cause, progressive neurologic disorder, uncontrolled epilepsy or progressive encephalopathy: pertussis vaccine should not be administered to individuals with these conditions until a treatment regimen has been established and the condition has stabilized.
  • History of transient thrombocytopenia or neurological complications following an earlier immunization against diphtheria and/or tetanus.
  • History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s) or having shown signs of hypersensitivity after previous administration of diphtheria, tetanus or pertussis vaccines.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination
  • Acute or unstable chronic conditions clinically significant pulmonary, cardiovascular, hepatic, or renal functional abnormality, as determined by physical examination and/or laboratory screening tests.
  • Any other clinical condition that, in the opinion of the investigator, might pose additional risk to the participant due to participation in the clinical study.
  • Condition that in the judgment of the investigator would make intramuscular injection unsafe.

Prior/Concomitant therapy

  • Use of any investigational or non-registered product other than the study intervention(s) during the period beginning 30 days before the dose of study intervention(s), or their planned use during the study period.
  • Administration of immunoglobulins or other blood products or plasma derivatives during the period starting 90 days before the study intervention or planned administration during the study period.
  • Chronic administration of immune-modifying drugs and/or planned use of long-acting immune-modifying treatments at any time up to the end of the study.

    • Up to 6 months prior to the study intervention administration:

For corticosteroids, this will mean prednisone equivalent ³0.5 mg/kg/day with maximum of 20 mg/day. Inhaled, intra-articular/intra-bursal and topical steroids are allowed.

  • Up to 6 months prior to study intervention administration: long-acting immune-modifying drugs including among others immunotherapy, monoclonal antibodies, antitumoral medication.

    • Planned administration/administration of a vaccine not foreseen by the study protocol in the period starting 30 days before the dose and ending 30 days after the dose of study intervention(s) administration*, with the exception of inactivated influenza vaccine and SARS-CoV-2 vaccine which can be given at any time during the study conduct.

      *If emergency mass vaccination for an unforeseen public health threat (e.g., a pandemic) is recommended and/or organized by public health authorities outside the routine immunization program, the time period described above can be reduced, provided it is used according to the local governmental recommendations and Sponsor is notified.

    • Planned administration of any prophylactic medication in the absence of any symptom and in anticipation of a reaction to the study intervention administration.

Prior/Concurrent clinical study participation

• Concurrently participating in another clinical study, at any time during the study period, in which the participant has been or will be exposed to an investigational or a non-investigational intervention vaccine/drug/invasive medical device.

Other exclusion criteria

  • Pregnant or lactating participant.
  • History of /current chronic alcohol consumption and/or drug abuse, based on investigator's judgment.
  • Any study personnel or their immediate dependents, family, or household members.
  • Child in care.

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:非随机化
  • 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:dTpa Group
Participants aged 11 to less than (<) 13 years receive the dTpa vaccine at Day 1.
Combined reduced antigen content diphtheria, tetanus and acellular pertussis (dTpa) vaccine administered at Day 1.

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
Number of seropositive participants for anti-pertussis toxin (anti-PT), anti-filamentous hemagglutinin (FHA) and anti-pertactin (PRN) antibodies
大体时间:1 month after vaccination
Seropositivity is defined as antibody concentrations (anti-PT, anti-FHA and anti-PRN) are greater than or equal to the assessed assay cut-offs. The considered cut-off values are: anti-PT: 2.693 International Units per milliliter (IU/mL), anti-FHA: 2.046 IU/mL, anti-PRN: 2.187 IU/mL, as measured by Enzyme-Linked Immunosorbent assay (ELISA).
1 month after vaccination
Number of seroprotected participants for anti-diphteria and anti-tetanus antibodies
大体时间:1 month after vaccination
Seroprotection is defined as anti-diphtheria and anti- tetanus antibody concentrations being >=0.1 IU/mL as measured by ELISA.
1 month after vaccination

次要结果测量

结果测量
措施说明
大体时间
Number of participants with booster-response to pertussis (PT, FHA and PRN) antigens
大体时间:1 month after vaccination
Booster response to PT, FHA and PRN antigens is defined as: for participants with pre-vaccination antibody concentration below the assay cut-off, post-vaccination antibody concentration >=4 times the assay cut-off; for participants with pre-vaccination antibody concentration between the assay cut-off and below 4 times the assay cut-off, post-vaccination antibody concentration >= 4 times the pre-vaccination antibody concentration; for participants with pre-vaccination antibody concentration >=4 times the assay cut-off, post-vaccination antibody concentration >=2 times the pre-vaccination antibody concentration.
1 month after vaccination
Antibody concentration against pertussis (PT, FHA, PRN) antigens
大体时间:At baseline (Day 1) and 1 month after vaccination
At baseline (Day 1) and 1 month after vaccination
Antibody concentration for anti-diphtheria and anti-tetanus antibodies
大体时间:At baseline (Day 1) and 1 month after vaccination
At baseline (Day 1) and 1 month after vaccination
Number of participants with solicited local adverse events (AEs)
大体时间:From Day 1 (day of vaccination) to Day 7 post-vaccination
Solicited local AEs are pain, redness (erythema) and swelling at administration site.
From Day 1 (day of vaccination) to Day 7 post-vaccination
Number of participants with solicited systemic AEs
大体时间:From Day 1 (day of vaccination) to Day 7 post-vaccination
Solicited systemic AEs are fever, headache, myalgia (muscle pain), arthralgia (joint pain), fatigue (tiredness) and gastrointestinal symptoms.
From Day 1 (day of vaccination) to Day 7 post-vaccination
Number of participants with unsolicited AEs
大体时间:From Day 1 (day of vaccination) to Day 30 post-vaccination
An unsolicited AE is an AE that was either not included in the list of solicited AEs or could be included in the list of solicited AEs but with an onset outside the specified period of follow-up for solicited AEs. Unsolicited AEs include both serious and non-serious AEs.
From Day 1 (day of vaccination) to Day 30 post-vaccination
Number of participants with serious AEs (SAEs)
大体时间:From Day 1 (day of vaccination) to Day 30 post-vaccination
An SAE is defined as any untoward medical occurrence that, at any dose, results in death, is life threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect in the offspring of a study participant, abnormal pregnancy outcomes, is a suspected transmission of any infectious agent via an authorized medicinal product, or other situations as per investigator's judgment.
From Day 1 (day of vaccination) to Day 30 post-vaccination
Number of participants with AEs leading to study withdrawal
大体时间:From Day 1 (day of vaccination) to Day 30 post-vaccination
From Day 1 (day of vaccination) to Day 30 post-vaccination

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)

2026年6月29日

初级完成 (实际的)

2026年9月4日

研究完成 (实际的)

2026年9月4日

研究注册日期

首次提交

2026年5月13日

首先提交符合 QC 标准的

2026年5月13日

首次发布 (实际的)

2026年5月19日

研究记录更新

最后更新发布 (实际的)

2026年9月9日

上次提交的符合 QC 标准的更新

2026年9月7日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Study Sponsor will assess requests from qualified researchers for anonymized individual patient-level data and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf

IPD 共享时间框架

Anonymized IPD will be made available within 6 months of publication of primary, key secondary and safety results for studies in product with approved indication(s) or asset(s) with development terminated across all indications.

IPD 共享访问标准

Anonymized IPD is shared with researchers whose proposals are approved by an Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months, but an extension may be granted, when justified, for up to 6 months.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 企业社会责任

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.

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