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RSVPreF3 OA vaccine
RSVPreF3 OA vaccine is a Recombinant protein vaccine Biologic drug developed by GlaxoSmithKline. It is currently in Phase 3 development for Prevention of respiratory syncytial virus (RSV) disease in older adults (≥60 years), Prevention of RSV disease in infants via maternal immunization (under investigation).
RSVPreF3 OA is a recombinant protein vaccine that presents a stabilized prefusion form of the respiratory syncytial virus (RSV) F glycoprotein to elicit protective immune responses against RSV infection.
RSVPreF3 OA is a recombinant protein vaccine that presents a stabilized prefusion form of the respiratory syncytial virus (RSV) F glycoprotein to elicit protective immune responses against RSV infection. Used for Prevention of respiratory syncytial virus (RSV) disease in older adults (≥60 years), Prevention of RSV disease in infants via maternal immunization (under investigation).
At a glance
| Generic name | RSVPreF3 OA vaccine |
|---|---|
| Sponsor | GlaxoSmithKline |
| Drug class | Recombinant protein vaccine |
| Target | RSV F glycoprotein (prefusion conformation) |
| Modality | Biologic |
| Therapeutic area | Immunology / Infectious Disease |
| Phase | Phase 3 |
Mechanism of action
The vaccine uses a rationally designed prefusion-stabilized RSV F protein (PreF3) formulated with an oil-in-water adjuvant (OA) to enhance immunogenicity. This design aims to induce robust antibody and T-cell responses that neutralize RSV and prevent infection or severe disease. The prefusion conformation is believed to be more immunogenic and closer to the native viral structure than postfusion forms.
Approved indications
- Prevention of respiratory syncytial virus (RSV) disease in older adults (≥60 years)
- Prevention of RSV disease in infants via maternal immunization (under investigation)
Common side effects
- Injection site pain
- Injection site erythema
- Myalgia
- Fatigue
- Headache
Key clinical trials
- Immunogenicity, Safety, Reactogenicity and Persistence of an Investigational Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 60 Years and Above (PHASE3)
- A Study on the Immune Response and Safety of Vaccine Against Respiratory Syncytial Virus Given to Chinese Adults 18 to 59 Years of Age at Increased Risk of Respiratory Syncytial Virus Disease (PHASE3)
- An Extension and Crossover Vaccination Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus Given to Adults 60 Years of Age and Above Who Participated in RSV OA=ADJ-006 Study (PHASE3)
- A Study Evaluating Persistence of the Immune Response of the Adjuvanted Respiratory Syncytial Virus (RSV) Vaccine and the Safety and Immune Response Following Revaccination in Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant (PHASE2)
- A Study on the Immune Response, Safety and the Occurrence of Respiratory Syncytial Virus (RSV)-Associated Respiratory Tract Illness After Administration of RSV OA Vaccine in Adults 60 Years and Older (PHASE3)
- A Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus (RSV) When Given Alone and Together With a COVID-19 mRNA Vaccine in Adults Aged 50 Years and Above (PHASE3)
- A Study in India on the Immune Response and Safety of a Respiratory Syncytial Virus (RSV) Older Adults (OA) Vaccine When Given to Older Adults 60 Years of Age and Above and Adults 50-59 Years of Age at Increased Risk (AIR) of Respiratory Syncytial Virus Lower Respiratory Tract Disease (RSV-LRTD) (PHASE3)
- A Study on the Immune Response and Safety of Vaccine Against Respiratory Syncytial Virus (RSV) Given to Adults 18 to 49 Years of Age at Increased Risk for Respiratory Syncytial Virus Disease, Compared to Older Adults 60 Years of Age and Above (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- RSVPreF3 OA vaccine CI brief — competitive landscape report
- RSVPreF3 OA vaccine updates RSS · CI watch RSS
- GlaxoSmithKline portfolio CI
Frequently asked questions about RSVPreF3 OA vaccine
What is RSVPreF3 OA vaccine?
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What does RSVPreF3 OA vaccine target?
Related
- Drug class: All Recombinant protein vaccine drugs
- Target: All drugs targeting RSV F glycoprotein (prefusion conformation)
- Manufacturer: GlaxoSmithKline — full pipeline
- Therapeutic area: All drugs in Immunology / Infectious Disease
- Indication: Drugs for Prevention of respiratory syncytial virus (RSV) disease in older adults (≥60 years)
- Indication: Drugs for Prevention of RSV disease in infants via maternal immunization (under investigation)
- Compare: RSVPreF3 OA vaccine vs similar drugs
- Pricing: RSVPreF3 OA vaccine cost, discount & access