A Study to Evaluate the Different Doses of VAC52416 (ExPEC10V) in Japanese Adults

Janssen Pharmaceutical K.K.24 enrolled

Overview

The purpose of this study is to evaluate the safety and reactogenicity of different doses of extraintestinal pathogenic Escherichia coli 10 valent (ExPEC10V) in Japanese participants greater than or equal to (\>=) 60 to less than or equal to (\<=) 85 years of age.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

DOUBLE

Enrollment

Conditions

Healthy

Interventions

ExPEC10VBIOLOGICAL

Participants will receive a single IM injection of ExPEC10V.

PlaceboBIOLOGICAL

Participants will receive single IM injection of matching placebo.

Eligibility

Sex: ALLMin age: 60 YearsMax age: 85 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Participant must be Japanese as determined by participant's verbal report * Must be healthy or medically stable, in the investigator's clinical judgment, as confirmed by medical history, physical examination, vital signs, 12-lead electrocardiogram (ECG), and clinical laboratory tests performed at the screening visit * Willing and able to adhere to the lifestyle restrictions * Agrees not to donate blood until 12 weeks after receiving the study intervention * Must be willing to provide verifiable identification, has means to be contacted, and to contact the investigator during the study Exclusion Criteria: * Clinically significant illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature greater than or equal to (\>=) 38.0 degree Celsius (100.4 degree Fahrenheit ) within 24 hours prior to the administration of study intervention; enrollment at a later date is permitted (provided the screening window of 28 days is respected) * History of malignancy within 5 years before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or malignancy, which is considered cured with minimal risk of recurrence) * Known allergies, hypersensitivity, or intolerance to ExPEC10V or its excipients * Known allergy or history of anaphylaxis or other serious adverse reactions to vaccines or vaccine excipients * Contraindication to Intramuscular (IM) injections and blood draws example, bleeding disorders

Locations (1)

SOUSEIKAI PS Clinic

Fukuoka, Japan

Outcomes

Primary Outcomes

Number of Participants with Solicited Local Adverse Events (AEs) Collected for 14 days post-Vaccination

Number of participants with solicited local AEs will be reported. Solicited local AEs (pain/tenderness, erythema, and swelling at the injection site) and will be noted in the participant diary for 14 days post-vaccination.

Time frame: 14 days post-Vaccination (Up to Day 15)

Number of Participants with Solicited Systemic AEs Collected for 14 days post-Vaccination

Number of participants with solicited systemic AEs will be reported. Solicited systemic AEs (oral body temperature, headache, fatigue, nausea, and myalgia) will be noted in the participant diary for 14 days post-vaccination.

Time frame: 14 days post-Vaccination (Up to Day 15)

Number of Participants with Unsolicited AEs From the Administration of Study Vaccine until 29 Days post-Vaccination

Number of participants with unsolicited AEs will be reported. Unsolicited AEs are all AEs for which the participant is not specifically questioned in the participants diary.

Time frame: From the administration of study vaccine until 29 days post-Vaccination (Up to Day 30)

Number of Participants with Serious AEs from the Administration of the Study Vaccine until Day 181

Number of participants with SAEs will be reported. A SAE is any AE that results in: death, persistent or significant disability/incapacity, requires inpatient hospitalization or prolongation of existing hospitalization, is life threatening experience, is a congenital anomaly/birth defect, is suspected transmission of any infectious agent via a medicinal product, is medically important, and may jeopardize participant or may require medical or surgical intervention to prevent one of the outcomes listed above.

Time frame: From the administration of study vaccine until 180 days post-Vaccination (Up to Day 181)

Secondary Outcomes

Data from ClinicalTrials.gov

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