BENITIONSClinical Trial Intelligence

Immunogenicity, Safety, Reactogenicity and Persistence of an Investigational Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 60 Years and Above

Фаза 3 Идёт, набор закрыт NCT04732871

ЗаболеваниеRespiratory Syncytial Virus Infections
ФазаФаза 3
СпонсорGlaxoSmithKline
СтатусИдёт, набор закрыт
Участники1,720 участн.
ВмешательствоRSVPreF3 OA investigational vaccine
Дата начала15.02.2021
Дата завершения6.06.2022
Публикация результатов21.12.2023

Кратко

The purpose of this study is to assess the safety, reactogenicity, immunogenicity and long-term persistence of immune response up to 5 years following a single dose vaccination of GSK's investigational vaccine RSVPreF3 OA, in adults aged 60 years and above. The study will also evaluate the immunogenicity, safety and reactogenicity of additional vaccine doses given according to different revaccination schedules.

Humoral Immune Response in Terms of Respiratory Syncytial Virus (RSV)-A Neutralizing Antibody Geometric Mean Titers (GMTs) at Day 1

At Day 1 · Titers (ED60)

RSV_annual832.4 Titers (ED60)
RSV_flexible Revaccination864.9 Titers (ED60)
RSV_1dose896.8 Titers (ED60)

Humoral Immune Response in Terms of RSV-A Neutralizing Antibody GMTs at Day 31

At Day 31 · Titers (ED60)

RSV_annual8827.2 Titers (ED60)
RSV_flexible Revaccination8906.6 Titers (ED60)
RSV_1dose9585.6 Titers (ED60)

Humoral Immune Response in Terms of RSV-A Neutralizing Antibody GMTs at Month 6

At Month 6 · Titers (ED60)

RSV_annual3465.2 Titers (ED60)
RSV_flexible Revaccination3600.1 Titers (ED60)
RSV_1dose4223.1 Titers (ED60)

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