BENITIONSClinical Trial Intelligence

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

3상 진행 중(모집 완료) NCT04732871

대상 질환Respiratory Syncytial Virus Infections
임상 단계3상
스폰서GlaxoSmithKline
상태진행 중(모집 완료)
참여자 수1,720 명
중재(약물)RSVPreF3 OA investigational vaccine
시작일2021년 2월 15일
완료일2022년 6월 6일
결과 공개일2023년 12월 21일

요약

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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