U.S. FDA Accepts for Priority Review Pfizer’s Application for TicoVac™ (Tick-borne Encephalitis Vaccine)

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Tick-borne encephalitis (TBE) is a viral infection, endemic to parts of Europe and Asia

If approved, the vaccine may help reduce the risk of TBE for people traveling to endemic areas, potentially including military personnel serving in these locations

NEW YORK – Pfizer Inc. (NYSE:PFE) today announced that the U.S. Food and Drug Administration (FDA) accepted for Priority Review the company’s Biologics License Application (BLA) for TicoVac™, its tick-borne encephalitis (TBE) vaccine for active immunization to prevent TBE in individuals 1 year of age and older.1,2 If approved, TicoVac would be the first vaccine in the U.S. to help protect adults and children who are visiting or living in TBE endemic areas. In line with Priority Review designation, the FDA will target an action within six months of the application submission date,3 with the anticipated Prescription Drug User Fee Act (PDUFA) action date expected for August 2021.

TBE is a viral infection of the brain and spine,4 which is transmitted to humans through the bite of an infected tick.5 To date, ticks infected with the TBE virus have been identified in more than 35 countries across Europe and Asia.5 The European Centre for Disease Prevention and Control (ECDC) currently recommends TBE vaccination for people who live in or are traveling to these risk areas.6

“For many years, our TBE vaccine has helped protect millions of people in Europe from this potentially serious disease. We are proud that today’s U.S. FDA Priority Review acceptance acknowledges the potential value that our vaccine candidate can bring,” said Nanette Cocero, Ph.D., Global President, Vaccines, Pfizer Inc. “If approved in the U.S., we hope this vaccine will help protect those traveling to or residing temporarily in at-risk locations, potentially including military personnel who are serving overseas.”

The BLA is based on results from more than 40 years of experience and evidence outside the U.S.7 In clinical trials, the safety and immunogenicity of TicoVac was assessed across two age groups (1-15 years of age and 16-65 years of age).7 In these studies, pooled seropositivity rates were 99-100% in 1-15 year olds and 94-99% in adults >15 years following three doses.*8,9 Clinical studies demonstrated that TicoVac was well-tolerated with no unexpected adverse events or vaccine-related serious adverse events observed.8,9 Subsequent real-world studies have shown that the vaccine is 96-99% effective in people who have received at least two doses of the vaccine,10,11 and two to three doses of the vaccine were shown to be sufficient to provide a long-lasting immune memory.1,2,12

About TicoVac™ (TBE vaccine, whole virus inactivated)

Pfizer’s TBE vaccine, marketed under the brand names TicoVac and FSME-Immun™ in Europe, is an inactivated whole virus vaccine developed using a master ‘seed’ virus that is similar to the TBE virus found in nature.13 Therefore, it is able to induce neutralizing antibodies against the natural TBE virus, as the sequence and structure of the virus subtype match those found in nature.14 The vaccine helps provide protection against all known subtypes of the TBE virus in both children (from one year of age) and adults,1,2,14 including the European, Siberian and Far Eastern subtypes.15,16

More than 40 years of experience with the Pfizer TBE vaccine exist outside the U.S., and more than 160 million doses of the vaccine have been distributed since 1976.7,17

About TBE

TBE is a viral infection of the brain and spine,4 transmitted to humans through the bite of an infected tick,5 and less frequently by ingestion of unpasteurized milk or milk products from infected animals.4 It may initially be mistaken for summer flu,18,19 but can be a serious condition with possible long-term consequences.4,19 More than 1 in 3 people can have long-term effects that last months or years including cognitive changes, muscle weakness or permanent paralysis,4,19 and in rare cases (0.5-2%; up to 20% in Russia), people may die.20,21 TBE can affect people of all ages who come into contact with ticks whenever they do outdoor activities in countries where ticks infected with TBE are prevalent.4,21

Although TBE is not endemic in the U.S., TBE has been reported in more than 35 countries, ranging from Western Europe to Japan.5 Currently there is no cure or treatment for TBE, only management of symptoms.4 The potential vaccine could help protect people from the U.S. who are traveling to or living in endemic regions.

About Pfizer: Breakthroughs That Change Patients’ Lives

At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world’s premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 170 years, we have worked to make a difference for all who rely on us. We routinely post information that may be important to investors on our website at www.Pfizer.com. In addition, to learn more, please visit us on www.Pfizer.com and follow us on Twitter at @Pfizer and @Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook.com/Pfizer.

References

  1. TicoVac® Summary of Product Characteristics. Last updated: November 2018.
  2. TicoVac® Junior Summary of Product Characteristics. Last updated: November 2018.
  3. U.S Food & Drug Administration. Priority Review. Available from: https://www.fda.gov/patients/fast-track-breakthrough-therapy-accelerated-approval-priority-review/priority-review. Accessed: February 2021.
  4. Lindquist L, et al. Tick-borne encephalitis. The Lancet. 2008;371(9627):1861-71.
  5. Dobler G, Erber W, Bröker M, Schmitt HJ, eds. The TBE Book. 3rd ed. Singapore: Global Health Press; 2020. doi:10.33442/26613980_1-3. Available from: https://tbenews.com/tbe/. Accessed: May 2020.
  6. European Centre for Disease Prevention and Control. Key messages about tick-borne encephalitis and tick-borne diseases. Available from: https://ecdc.europa.eu/en/tick-borne-encephalitis/facts/key-messages. Accessed: February 2021.
  7. Loew-Baselli A, et al. Prevention of tick-borne encephalitis by FSME-IMMUN vaccines: review of a clinical development programme. Vaccine. 2011;29(43):7307-19.
  8. Ehrlich HJ, et al. Randomized, phase II dose-finding studies of a modified tick-borne encephalitis vaccine: evaluation of safety and immunogenicity. Vaccine. 2003 Dec 12;22(2):217-23.
  9. Pöllabauer EM, et al. Clinical evaluation to determine the appropriate paediatric formulation of a tick-borne encephalitis vaccine. Vaccine. 2010 Jun 23;28(29):4558-65.
  10. Heinz FX, et al. Field effectiveness of vaccination against tick-borne encephalitis. Vaccine. 2007;25(43):7559-67.
  11. Heinz FX, et al. Vaccination and tick-borne encephalitis, central Europe. Emerg Infect Dis. 2013;19(1):69-76.
  12. Schosser R, et al. Irregular tick-borne encephalitis vaccination schedules: the effect of a single catch-up vaccination with FSME-IMMUN®. A prospective non-interventional study. Vaccine. 2014;32(20):2375-81.
  13. Barrett PN. Tick-borne encephalitis virus vaccines, p 773–88. In: Plotkin SA, Orenstein WA, PA O, (ed). Vaccines Sixth edition.
  14. Elsevier Saunders; 2013, Philadelphia, PA.
  15. Orlinger KK, et al. A tick-borne encephalitis virus vaccine based on the European prototype strain induces broadly reactive cross-neutralizing antibodies in humans. J Infect Dis. 2011;203(11):1556-64.
  16. Adelshin RV, et al. Complete Genome Sequences of Four European Subtype Strains of Tick-Borne Encephalitis Virus from Eastern Siberia, Russia. Genome Announc. 2015;3(3).
  17. Tonteri E, et al. Tick-borne encephalitis virus in wild rodents in winter, Finland, 2008-2009. Emerg Infect Dis. 2011;17(1):72-5.
    Pfizer. Data on file. 2020 FSME-IMMUN doses.
  18. Travel Health Pro. Country information. Tick borne encephalitis. Available from: https://travelhealthpro.org.uk/disease/173/tick-borne-encephalitis. Accessed: February 2021.
  19. Kaiser R. Tick-borne encephalitis. Infect Dis Clin North Am. 2008;22(3):561-75.
  20. Santos R., Monteiro S. Epidemiology, control, and prevention of emerging zoonotic viruses. Viruses in Food and Water. 2013:442-457.
  21. European Centre for Disease Prevention and Control. Factsheet about tick-borne encephalitis. Available from: https://www.ecdc.europa.eu/en/tick-borne-encephalitis/facts/factsheet. Accessed: February 2021.
    * Seropositivity measured by neutralising antibody titers (NT) and enzyme-linked immunosorbent assay (ELISA) responses.

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