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Table 1 Phase 3 vaccine efficacy data of Arexvy® and Abrysvo® and the efficacy values of an RSV hypothetical vaccine

From: Influential drivers of the cost-effectiveness of respiratory syncytial virus vaccination in European older adults: a multi-country analysis

Arexvy® (GSK)

Abrysvo® (Pfizer)

Endpoints

Season 1 (full season)

Season 2 (full season)

Endpoints

Season 1 (full season)

Season 2 (full season)

   

ARI ≥1 symptom

62.1% (95% CI 37.1–77.9)

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ARI ≥2 symptoms or sign

71.7% (95% CI 56.2–82.3)

40.6% (95% CI 19.0–57.0)

   

LRTD ≥2 symptoms including ≥1 sign or ≥3 symptoms

82.6% (96.95% CI 57.9–94.1)

56.1% (95% CI 28.2–74.4)

LRTD ≥2 symptoms or signs

66.7% (96.66% CI 28.8–85.8)

55.7% (95% CI 34.7–70.4)

LRTD ≥3 symptoms or signs

85.7% (96.66% CI 32.0–98.7)

77.8% (95% CI 51.4–91.1)

Severe LRTD (≥2 signs or defined as severe by investigator)

94.1% (95% CI 62.4–99.9)

64.2% (95% CI 61.6–93.4%)

   

RSV hypothetical vaccine

Vaccine efficacy against

Season 1 (full season)

Season 2 (full season)

Non-MA

65% (35–85%)

35% (15–60%)

Primary care

65% (35–85%)

35% (15–60%)

Hospitalisation

80% (35–95%)

55% (25–80%)

Death

90% (60–100%)

60% (55–95%)

  1. Abbreviations: ARI acute respiratory infection, LRTD lower respiratory tract disease