GSK's Arexvy RSV Vaccine: Three-Year Efficacy and CDC Recommendations Challenges

GSK's Arexvy vaccine represents a significant advancement as the first market entrant for RSV, targeting older adults 60 and above. The vaccine demonstrated a cumulative efficacy of 62.9% against RSV-associated lower respiratory tract disease (LRTD) across three seasons, with an efficacy of 67.4% against severe cases[1][2]. However, effectiveness declined to 48% during the third season, highlighting the potential need for revaccination, though currently, a second dose is not recommended by the CDC[2]. Despite the vaccine's success, the CDC's narrower recommendations, due to potential links to Guillain-Barré syndrome, pose challenges, affecting projected market values[1].
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Explore Further
How does GSK plan to address the efficacy decline of the Arexvy vaccine in its third season?
What specific safety concerns led the CDC to narrow its recommendations for the Arexvy vaccine?
In what ways is GSK responding to competition from Pfizer and Moderna in the RSV vaccine market?
What are the potential implications for GSK's market share if revaccination becomes necessary for Arexvy?
How might the CDC's advisory concerning Guillain-Barré syndrome impact the future development of similar vaccines?