BENITIONSClinical Trial Intelligence

A Study on the Immunogenicity and Safety of 3 Different Dose Concentrations of a Respiratory Syncytial Virus Vaccine in Infants and Toddlers

Фаза 3 Прекращено NCT06705140

ЗаболеваниеRSV Immunisation, Healthy Volunteers
ФазаФаза 3
СпонсорSanofi Pasteur, a Sanofi Company
СтатусПрекращено
Участники42 участн.
ВмешательствоLow Dose (LD) RSVt vaccine, Standard Dose (SD) RSVt vaccine, High Dose (HD) RSVt vaccine
Дата начала25.11.2024
Дата завершения11.06.2025
Публикация результатов3.08.2026

Кратко

This study was a Phase III, parallel group, randomized, observer blind, placebo controlled, multi-national, multi-center, multi-arm study conducted in 42 healthy children enrolled at 6 months to \<22 months of age. The purpose of the study was to evaluate the non-inferiority of the immune response of the lower dose (LD) when compared to the standard dose (SD) respiratory syncytial virus infant and toddler (RSVt) vaccine and the safety of the LD, SD and high dose (HD) vaccine in preterm born children and of the HD vaccine in full term born children administered by intranasal route and compared to placebo.

Cohort 2: Geometric Mean Titers (GMT) of RSV A Serum Neutralizing Antibodies at Day 85 (Post-Dose 2)

Day 85 (28 days post-vaccination 2)

Cohort 2: Geometric Mean Titers of RSV B Serum Neutralizing Antibodies at Day 85 (Post-Dose 2)

Day 85 (28 days post-vaccination 2)

Cohorts 1 and 2: Number of Participants With Immediate Unsolicited Systemic Adverse Events (AEs)

Up to 30 minutes after each vaccination (post-dose on Day 1) · Participants

Cohort 1: Group 1: Standard Dose RSVt0 Participants
Cohort 1: Group 2: Placebo0 Participants
Cohort 2: Group 1: Low Dose RSVt0 Participants
Cohort 2: Group 2: Standard Dose RSVt0 Participants
Cohort 2: Group 3: High Dose RSVt0 Participants
Cohort 2: Group 4: Placebo0 Participants

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