Seqirus, a global leader in influenza prevention and a division of CSL Limited (ASX: CSL), today announced that the company co-authored the first study to demonstrate the safety, immunogenicity and efficacy profile of a COVID-19 vaccine when co-administered with a seasonal influenza vaccine
SUMMIT, N.J., June 14, 2021 /PRNewswire/ -- Seqirus, a global leader in influenza prevention and a division of CSL Limited (ASX: CSL), today announced that the company co-authored the first study to demonstrate the safety, immunogenicity and efficacy profile of a COVID-19 vaccine when co-administered with a seasonal influenza vaccine.1 The data is now available on medRxiv ahead of peer-review publication.1 The study was conducted by Novavax, Inc. as part of a Phase 3 clinical trial of NVX-CoV2373, its recombinant protein COVID-19 vaccine candidate, in the United Kingdom.1 The co-administration sub-study enrolled 431 volunteers, all of whom received either an adjuvanted, trivalent seasonal influenza vaccine (aTIV) or a cell-based, quadrivalent seasonal influenza vaccine (QIVc) provided by Seqirus.1 Approximately half of the volunteers also received NVX-CoV2373 while the remainder received the placebo. The study results suggest that efficacy of both the influenza vaccine and the COVID-19 vaccine candidate appeared to be preserved.1 No additional safety concerns were found with co-administration and adverse events were similar to the incidence and severity for each vaccine when administered separately.1 “These data could be used to help inform guidance or recommendations on the co-administration of influenza and COVID-19 vaccines, overcoming challenges and contributing towards a new normal to protect at-risk populations from both infections,” said Raja Rajaram, M.D., Medical Affairs Lead, EMEA, Seqirus, a co-author of the study. “Seqirus is committed to advancing the science underpinning influenza and taking our place on the front line, alongside our public health partners, as a reliable influenza vaccine supplier.” Seqirus’ seasonal influenza vaccines have a well-established safety profile, and although additional research is needed, results of this study suggest that concomitant vaccination may be a viable immunization strategy.1 Participation in this co-administration study demonstrates the company’s commitment to supporting informed, science-based decisions regarding vaccinations for patients. Study limitations include the small size of the sub-study, lack of formal pre-specified non-inferiority statistical assessment of immunogenicity, and the lack of randomization in recruiting the influenza sub-study, immunogenicity and reactogenicity cohorts.1 “With large scale COVID-19 vaccination campaigns underway in many countries across the globe, and as mitigation tactics like social distancing become more relaxed, we need to be prepared for the resurgence of influenza activity,” said Gregg Sylvester, M.D., Chief Medical Officer at Seqirus. “As a company on the front line of influenza prevention, we’re committed to helping protect our communities with our differentiated portfolio of safe and effective influenza vaccines.” Seqirus appreciates the opportunity to partner with Novavax on this important study. “As the next influenza season approaches and people still need a primary COVID-19 vaccine series or a booster, separate healthcare visits to cover both COVID-19 and influenza vaccinations will be burdensome,” said Gregory M. Glenn, M.D., President of Research and Development, Novavax. “As the first clinical study to evaluate safety, immunogenicity, and efficacy of a COVID-19 vaccine when co-administered with a seasonal influenza vaccine, these results demonstrate the promising opportunity for concomitant vaccination, which may improve the uptake of both vaccines.” Seqirus produces influenza vaccines across its global manufacturing network, which includes facilities in the U.S., U.K. and Australia. Since the start of the COVID-19 pandemic, the company has experienced record demand for influenza vaccines across all markets and has extended production across its three manufacturing sites. About Seasonal Influenza About Seqirus About CSL For more information visit www.seqirus.com and www.csl.com. Intended Audience Forward-Looking Statements USA-CRP-21-0038 Media Contact REFERENCES 1 Safety, Immunogenicity, and Efficacy of a COVID-19 Vaccine (NVX-CoV2373) Co-administered 2 CDC. (2019). Key Facts about Influenza (Flu). Retrieved from: https://www.cdc.gov/flu/about/keyfacts.htm. Accessed June 2021. 3 CDC. (2020). Key Facts About Seasonal Flu Vaccine. Retrieved from: https://www.cdc.gov/flu/prevent/keyfacts.htm. Accessed June 2021. 4 CDC. (2020). 2019-2020 U.S. Flu season: Preliminary burden estimates. Retrieved from: https://www.cdc.gov/flu/about/burden/preliminary-in-season-estimates.htm. Accessed June 2021. 5 CDC. (2020). Who Needs a Flu Vaccine and When. Retrieved from: https://www.cdc.gov/flu/prevent/vaccinations.htm. Accessed June 2021. View original content:http://www.prnewswire.com/news-releases/seqirus-co-authors-first-study-to-assess-simultaneous-administration-of-seasonal-influenza-vaccine-and-covid-19-vaccine-candidate-301311885.html SOURCE Seqirus | ||
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