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A Study of Investigational RSV/hMPV Combination and Investigational hMPV Vaccines in Younger and Older Adults

2026年8月19日 更新者:GlaxoSmithKline

A Phase 1/2, Randomized, Controlled, Observer-blind, Multicentre Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of GSK Biologicals' Investigational Respiratory Syncytial Virus (RSV)/Human Metapneumovirus (hMPV) Combination and Investigational hMPV Vaccines When Administered Intramuscularly According to a Single Dose Schedule in Younger Adults ≥18 to ≤49 Years and Older Adults Aged ≥60 to ≤80 Years

The aim of this study is to evaluate the safety, reactogenicity, and immune response of the different formulations of the investigational RSV/hMPV combination vaccine and investigational hMPV vaccine in younger and older adults.

研究概览

研究类型

介入性

注册 (估计的)

1456

阶段

  • 阶段2
  • 阶段1

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

研究联系人备份

学习地点

    • New South Wales
      • Botany、New South Wales、澳大利亚、2019
        • 招聘中
        • GSK Investigational Site
        • 接触:
        • 接触:
        • 首席研究员:
          • Ronald Mak
    • Victoria
      • Camberwell、Victoria、澳大利亚、3124
        • 招聘中
        • GSK Investigational Site
        • 接触:
        • 接触:
        • 首席研究员:
          • Rishi Shah
    • Kansas
      • Lenexa、Kansas、美国、66219
        • 招聘中
        • GSK Investigational Site
        • 接触:
        • 接触:
        • 首席研究员:
          • Thomas Kreamer
    • Washington
      • Seattle、Washington、美国、98104
        • 招聘中
        • GSK Investigational Site
        • 接触:
        • 接触:
        • 首席研究员:
          • Nicole Ehrhardt

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

  • 成人
  • 年长者

接受健康志愿者

是的

描述

Inclusion criteria:

Participants are eligible to be included in the study only if all of the following criteria apply:

  • Written informed consent obtained from the participant prior to performance of any study-specific procedure.
  • Participants who can and will comply with the requirements of the protocol (e.g., completion of the eDiary, return for follow-up visits, ability to access and utilize a phone or other electronic communications).
  • Body Mass Index (BMI) between 18 kg/m^2 and 33 kg/m^2, inclusive.

Specific inclusion criteria for OA

  • A male or female between and including, 60 to 80 YOA at the time of the study intervention administration.
  • Healthy participants or medically stable patients as established by medical history and physical examination.

Specific inclusion criteria for YA

  • A male or female participant between and including 18 to 49 YOA at the time of the study intervention administration.
  • Healthy participants as established by medical history, clinical examination and laboratory assessment at screening.
  • 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 used two methods of contraception, at-least one of which must be a highly effective method, and the other being male condom for male sexual partners of POCBP to be used during sexual intercourse (with the exception of sexual abstinence, vasectomized partner and male partner who has been sterilized, in which case contraception is not required), at-least 30 days prior to study intervention administration, and has agreed to continue using above contraception requirements for 8 weeks after study intervention administration.
    • has a negative serum pregnancy test at screening and negative urine pregnancy test prior to study intervention administration on Day 1.

Exclusion criteria:

Participants are excluded from participating in the study if any of the following criteria apply:

  • History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s).
  • Any medical condition that in the judgment of the investigator would make IM injection unsafe.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease (e.g., current malignancy, HIV) or immunosuppressive/cytotoxic therapy (e.g., medication used during cancer chemotherapy, organ transplantation, or to treat autoimmune disorders), based on medical history and physical examination (no laboratory testing required).
  • Acute or unstable chronic pulmonary, cardiovascular, hepatic, or renal functional abnormality, as determined by physical examination and medical history.
  • Documented history of HIV, HBV, HCV infection.
  • History of RSV and /or hMPV-associated illness, diagnosed serologically or microbiologically in the last 12 months.
  • Recurrent history or uncontrolled neurological disorders or seizures, or history of demyelinating conditions (including GBS).
  • Any history of dementia or any medical condition that moderately or severely impairs cognition.
  • 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.
  • Significant underlying illness that in the opinion of the investigator would be expected to prevent completion of the study (e.g., life-threatening disease).
  • Use of any investigational or non-registered product (drug, vaccine, or invasive medical device) other than the study intervention during the period beginning 30 days before study intervention administration (Day -29 to Day 1), or within 5 half-lives, whichever is longer, or their planned use during the study period.
  • Has previously received an investigational or approved vaccine or antibody for prevention of hMPV and/or RSV-associated diseases.
  • Chronic administration of immune-modifying drugs (defined as more than 14 consecutive days in total) and/or planned use of long-acting immune-modifying treatments at any time up to the end of the study.

    • Up to 3 months prior to the study intervention administration:

      • For corticosteroids, this will mean prednisone equivalent >=20 mg/day for adult participants. Inhaled, topical and intra-articular steroids are allowed.
      • Administration of immunoglobulins and/or any blood products or plasma derivatives.
    • Up to 6 months prior to study intervention administration: long-acting immune-modifying drugs including among others immunotherapy (e.g., TNF-inhibitors), monoclonal antibodies, antitumoral medication.
  • 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.
  • History of chronic alcohol consumption and/or drug abuse as deemed by the investigator to render the potential participant unable/unlikely to provide accurate safety reports or comply with study procedures.
  • Participation of any study personnel or their immediate dependents, family, or household members.
  • Planned move during the study period that will prohibit participating in the study until study end.
  • Bedridden participants.

Specific exclusion criteria for OA population

  • Planned or actual administration of a vaccine not foreseen by the study protocol in the period beginning 30 days before study intervention administration (Day - 29 to Day 1), or their planned use 30 days after study intervention administration, with the exception of inactivated, subunit and split influenza vaccines or COVID-19 vaccines which can be administered up to 14 days before or from 14 days after the study intervention administration.
  • At screening (Phase 1 only), participants with:

    • >=Grade 2 abnormalities for the following parameters, regardless of clinical significance, should be excluded:

      • Hematologic: hemoglobin (Hb), white blood cells (WBC), platelets, absolute cell counts of lymphocytes, neutrophils, eosinophils,
      • Biochemical: alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), bilirubin, creatinine, blood urea nitrogen (BUN).
    • Grade 1/mild hematologic and/ or biochemical laboratory abnormalities that are not clinically significant in the clinical judgment of the investigator, may be included.

Specific exclusion criteria for YA population

  • Pregnant or lactating participant.
  • Female planning to become pregnant or planning to discontinue contraceptive precautions for 8 weeks after study intervention administration.
  • Planned or actual administration of a vaccine not foreseen by the study protocol in the period beginning 30 days before study intervention administration (Day - 29 to Day 1), or their planned use 30 days after study intervention administration.
  • At screening, participants with:

    • >=Grade 2 abnormalities for the following parameters, regardless of clinical significance, should be excluded:

      • Hematologic: Hb, WBC, platelets, absolute cell counts of lymphocytes, neutrophils, eosinophils,
      • Biochemical: ALT, AST, ALP, bilirubin, creatinine, BUN.
    • Grade 1/mild hematologic and/ or biochemical laboratory abnormalities that are not clinically significant in the clinical judgment of the investigator, may be included.
  • Use of any medication, including prescription and non-prescription drugs or herbal remedies (such as St. John's wort) beginning 14 days (or 5 half-lives) prior to study intervention administration and/or planned administration during the study period. Certain medications may be permitted (Eg: contraceptives for POCBP).

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:随机化
  • 介入模型:顺序分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:RSV/hMPV_X_low dose_Ph1_Younger Adults (YA) Group
YA participants receive a single dose of RSV/hMPV_X low dose vaccine in Phase 1, at Day 1.
RSV/hMPV_X low dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_X_medium dose_Ph1_YA Group
YA participants receive a single dose of RSV/hMPV_X medium dose vaccine in Phase 1, at Day 1.
RSV/hMPV_X medium dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_X_high dose_Ph1_YA Group
YA participants receive a single dose of RSV/hMPV_X high dose vaccine in Phase 1, at Day 1.
RSV/hMPV_X high dose vaccine administered intramuscularly.
实验性的:hMPV_Y_high dose_Ph1_YA Group
YA participants receive a single dose of hMPV_Y high dose vaccine in Phase 1, at Day 1.
hMPV_Y high dose vaccine administered intramuscularly.
实验性的:hMPV_Z_low dose_Ph1_YA Group
YA participants receive a single dose of hMPV_Z low dose vaccine in Phase 1, at Day 1.
hMPV_Z low dose vaccine administered intramuscularly.
实验性的:hMPV_Z_medium dose_Ph1_YA Group
YA participants receive a single dose of hMPV_Z medium dose vaccine in Phase 1, at Day 1.
hMPV_Z medium dose vaccine administered intramuscularly.
实验性的:hMPV_Z_high dose_Ph1_YA Group
YA participants receive a single dose of hMPV_Z high dose vaccine in Phase 1, at Day 1.
hMPV_Z high dose vaccine administered intramuscularly.
有源比较器:Control Vaccine_Ph1_YA Group
YA participants receive a single dose of control vaccine in Phase 1, at Day 1.
Control vaccine administered intramuscularly.
安慰剂比较:Placebo_Ph1_YA Group
YA participants receive a single dose of placebo in Phase 1, at Day 1.
Placebo administered intramuscularly.
实验性的:hMPV_Y_low dose_Ph1_OA Group
OA participants receive a single dose of hMPV_Y low dose vaccine in Phase 1, at Day 1.
hMPV_Y low dose vaccine administered intramuscularly.
实验性的:hMPV_Z_low dose_Ph1_OA Group
OA participants receive a single dose of hMPV_Z low dose vaccine in Phase 1, at Day 1.
hMPV_Z low dose vaccine administered intramuscularly.
实验性的:hMPV_Z_medium dose_Ph1_OA Group
OA participants receive a single dose of hMPV_Z medium dose vaccine in Phase 1, at Day 1.
hMPV_Z medium dose vaccine administered intramuscularly.
实验性的:hMPV_Z_high dose_Ph1_OA Group
OA participants receive a single dose of hMPV_Z high dose vaccine in Phase 1, at Day 1.
hMPV_Z high dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_V_low dose_Ph1 and Ph2_Older Adults (OA) Group
OA participants receive a single dose of RSV/hMPV_V low dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_V low dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_V_medium dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_V medium dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_V medium dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_V_high dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_V high dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_V high dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_W_low dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_W low dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_W low dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_W_medium dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_W medium dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_W medium dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_W_high dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_W high dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_W high dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_X_low dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_X low dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_X low dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_X_medium dose_Ph1 and Ph2_OA Group
OA participants received a single dose of RSV/hMPV_X medium dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_X medium dose vaccine administered intramuscularly.
实验性的:RSV/hMPV_X_high dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of RSV/hMPV_X high dose vaccine in both Phase 1 and Phase 2, at Day 1.
RSV/hMPV_X high dose vaccine administered intramuscularly.
实验性的:hMPV_Y_medium dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of hMPV_Y medium dose vaccine in both Phase 1 and Phase 2, at Day 1.
hMPV_Y medium dose vaccine administered intramuscularly.
实验性的:hMPV_Y_high dose_Ph1 and Ph2_OA Group
OA participants receive a single dose of hMPV_Y high dose vaccine in both Phase 1 and Phase 2, at Day 1.
hMPV_Y high dose vaccine administered intramuscularly.
有源比较器:Control Vaccine_Ph1 and Ph2_OA Group
OA participants receive a single dose of control vaccine in both Phase 1 and Phase 2, at Day 1.
Control vaccine administered intramuscularly.
安慰剂比较:Placebo_Ph1 and Ph2_OA Group
OA participants receive a single dose of placebo in both Phase 1 and Phase 2, at Day 1.
Placebo administered intramuscularly.

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 Participants Reporting Solicited Administration Site Events
大体时间:Day 1 to Day 7
Solicited administration site events include pain, redness (erythema) and swelling at administration site.
Day 1 to Day 7
Number of Participants Reporting Solicited Systemic Events
大体时间:Day 1 to Day 7
Solicited systemic events include fever [defined as oral or axillary temperature greater than or equal to (>=) 38.0°C/100.4°F], headache, myalgia (muscle pain), arthralgia (joint pain) and fatigue (tiredness).
Day 1 to Day 7
Number of Participants Reporting Unsolicited Adverse Events (AEs)
大体时间:Day 1 to Day 30
An unsolicited AE is defined as an AE that was either not included in the list of solicited events or could be included in the list of solicited events but with an onset outside the specified period of follow up for solicited events. Unsolicited AEs include both serious and non-serious AEs.
Day 1 to Day 30
Number of Participants Reporting Medically Attended Adverse Events (MAAEs)
大体时间:Day 1 to Month 12
MAAE is defined as unscheduled visit to or from healthcare professional for any reason, including emergency room visits.
Day 1 to Month 12
Number of Participants Reporting Potential immune-mediated disorders (pIMDs)
大体时间:Day 1 to Month 12
pIMDs are a subset of AEs of Special Interest (AESIs) that include autoimmune disorders and other inflammatory and/or neurologic disorders of interest which may or may not have an autoimmune etiology.
Day 1 to Month 12
Number of Participants Reporting Hematological and Biochemical Laboratory Abnormalities
大体时间:At Day 1 (pre-vaccination) in Phase 1 groups
At Day 1 (pre-vaccination) in Phase 1 groups
Number of Participants Reporting Hematological and Biochemical Laboratory Abnormalities
大体时间:At Day 8 (post-vaccination) in Phase 1 groups
At Day 8 (post-vaccination) in Phase 1 groups
Number of Participants Reporting Serious Adverse Events (SAEs)
大体时间:Day 1 to study end [Month 24 for OA groups (only the selected formulation group & its comparators) and Month 12 for all other YA groups & OA groups]
An SAE is any untoward medical occurrence that results in death, is life-threatening, requires 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, is an abnormal pregnancy outcome, or is a suspected transmission of any infectious agent via an authorized medicinal product.
Day 1 to study end [Month 24 for OA groups (only the selected formulation group & its comparators) and Month 12 for all other YA groups & OA groups]

次要结果测量

结果测量
措施说明
大体时间
Number of participants with hMPV neutralization titers equal to or above (>=) the assay cut-off value
大体时间:At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
Geometric mean titers (GMTs) of hMPV neutralization titers
大体时间:At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
Mean geometric increase (MGI) of hMPV neutralization titers
大体时间:At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
Seroresponse rate (SRR) against hMPV
大体时间:At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
SRR is defined as the number of participants having >=4-fold increase post-vaccination in neutralization titers against hMPV.
At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
Number of participants with RSV-A neutralization titers >= assay cut-off value
大体时间:At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
GMTs of RSV-A neutralization titers
大体时间:At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
MGI of RSV-A neutralization titers
大体时间:At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
SRR against RSV-A
大体时间:At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
SRR is defined as number of participants having >=4-fold-increase post-vaccination in neutralization titers against RSV-A.
At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
Number of participants with RSV-B neutralization titers >= assay cut-off value
大体时间:At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
GMTs of RSV-B neutralization titers
大体时间:At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
At Day 1 (pre-vaccination), Day 8 and Day 31 in OA groups included in both Phase 1 and Phase 2
MGI of RSV-B neutralization titers
大体时间:At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
SRR against RSV-B
大体时间:At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2
SRR is defined as number of participants having >=4-fold-increase post-vaccination in neutralization titers against RSV-B.
At Day 8 and Day 31 compared to Day 1 (pre-vaccination) in OA groups included in both Phase 1 and Phase 2

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5日

初级完成 (估计的)

2029年4月5日

研究完成 (估计的)

2029年4月5日

研究注册日期

首次提交

2026年5月26日

首先提交符合 QC 标准的

2026年5月26日

首次发布 (实际的)

2026年6月4日

研究记录更新

最后更新发布 (实际的)

2026年8月20日

上次提交的符合 QC 标准的更新

2026年8月19日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 223960
  • 2025-524456-58 (其他标识符:EU CT Number)

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

是的

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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