A Phase 3, randomized, placebo-controlled, observer-blind, multi-country study to demonstrate the efficacy of a single dose and annual revaccination doses of GSK's RSVPreF3 OA investigational vaccine in adults aged 60 years and above.
Latest Information Update: 08 Feb 2026
At a glance
- Drugs Respiratory syncytial virus vaccine adjuvanted (Primary)
- Indications Respiratory syncytial virus infections
- Focus Registrational; Therapeutic Use
- Acronyms AReSVi 006; RSV OA=ADJ-006
- Sponsors GlaxoSmithKline Biologicals; GSK
Most Recent Events
- 26 Jan 2026 According to a GSK plc media release, company has announced that its adjuvanted recombinant respiratory syncytial virus (RSV) vaccine, Arexvy, has been approved by the European Commission (EC) for use in adults aged 18 years and older.
- 08 Oct 2024 Results published in a GSK plc media release
- 08 Oct 2024 According to a GSK plc media release, new data from AReSVi-006 trial will be presented today at the CHEST 2024 Annual Meeting, organised by the American College of Chest Physicians. In addition to the presentation at CHEST, the data will be submitted for scientific peer-reviewed publication and to regulators for review.