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GSK and CureVac Announce Positive Phase 2 Data for mRNA Seasonal Influenza Vaccine

  • GSK and CureVac's mRNA-based seasonal influenza vaccine program has demonstrated positive Phase 2 results, marking a significant step in novel vaccine development.
  • The vaccine showed an improved immune response compared to existing commercial vaccines, suggesting enhanced protection against influenza strains.
  • This collaboration leverages mRNA technology to potentially offer more effective and adaptable influenza vaccines, addressing a critical public health need.
  • Further clinical trials are planned to assess long-term efficacy and safety, paving the way for potential regulatory submissions.
GSK and CureVac have announced promising Phase 2 clinical trial results for their mRNA-based seasonal influenza vaccine program. The data indicate an improved immune response compared to currently available commercial vaccines, highlighting the potential of mRNA technology in enhancing influenza protection.
The Phase 2 trial assessed the safety and immunogenicity of the mRNA vaccine across various influenza strains. Participants receiving the mRNA vaccine demonstrated a statistically significant increase in neutralizing antibody titers against multiple influenza strains, indicating a broader and more robust immune response. These findings suggest that the mRNA vaccine could offer superior protection against seasonal influenza compared to traditional vaccines.
"These positive Phase 2 results underscore the potential of our mRNA technology to address the ongoing threat of seasonal influenza," said a CureVac spokesperson. "We are committed to advancing this program in collaboration with GSK to deliver more effective influenza vaccines to the public."
Influenza remains a significant global health challenge, with seasonal epidemics causing substantial morbidity and mortality. According to the World Health Organization, influenza epidemics result in an estimated 290,000 to 650,000 respiratory deaths annually worldwide. Current influenza vaccines have limitations in terms of strain coverage and effectiveness, particularly against drifted strains. The mRNA technology offers the advantage of rapid development and adaptation to emerging strains, potentially providing a more effective and timely response to influenza outbreaks.
The GSK and CureVac collaboration aims to leverage these advantages to create a next-generation influenza vaccine that provides broader and more durable protection. The companies are planning to initiate Phase 3 trials to further evaluate the efficacy and safety of the mRNA vaccine in a larger population. These trials will assess the vaccine's ability to reduce influenza infection rates and prevent severe outcomes, such as hospitalization and death.
The development of an effective mRNA influenza vaccine could have a significant impact on public health by reducing the burden of seasonal influenza and improving overall pandemic preparedness. The ongoing clinical trials will provide critical data to support regulatory submissions and potential licensure of the vaccine.
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[1]
CureVac Partner GSK Announces Positive Phase 2 Data from Seasonal Influenza mRNA ...
curevac.com · Sep 12, 2024

CureVac N.V.’s press release includes forward-looking statements about future events and results, such as potential vacc...

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