US FDA Approval Expands Arexvy Prescription Demographics to 50-59 Age Bracket

Monday, 10 June 2024, 21:02

The US FDA approval of Arexvy for use in the 50-59 age group signals a significant advancement for GSK. The expansion of the prescription demographic opens up new opportunities for the respiratory jab, potentially enhancing GSK's market performance and driving growth in the coming quarters.
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US FDA Approval Expands Arexvy Prescription Demographics to 50-59 Age Bracket

US FDA Approves Arexvy for 50-59 Age Group

The recent approval by the US FDA to allow Arexvy's prescription for patients aged between 50 and 59 marks a pivotal moment for GSK.

Key Highlights:

  • Expansion: Arexvy's approval for a wider age group signifies increased market potential.
  • Opportunities: GSK stands to benefit from the extended prescription demographic.
  • Impact: This move is expected to positively influence GSK's growth trajectory in the future.

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