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AREXVY phase 3 efficacy and annual revaccination study in adults aged 60 years and older

jRCT2031210109Phase 3Completed

Sponsor
GSK
Start
Jun 2021
Modality
Vaccines & Immunotherapeutics, Recombinant Proteins and Enzymes
01

Overview

Phase 3, randomised, single-blind trial in respiratory syncytial virus disease (RSV) comparing AREXVY with Placebo (2 arms). Primary endpoints: Primary efficacy endpoint and Reported vaccine efficacy against RSV-associated LRTD. Started Jun 2021; status: completed.

02

Drugs

GSK3003899A
03

Conditions

respiratory syncytial virus disease (RSV)

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