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Last Updated: January 6, 2025

TICOVAC Drug Profile


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Summary for Tradename: TICOVAC
High Confidence Patents:0
Applicants:1
BLAs:1
Recent Clinical Trials: See clinical trials for TICOVAC
Recent Clinical Trials for TICOVAC

Identify potential brand extensions & biosimilar entrants

SponsorPhase
University of SurreyPhase 4

See all TICOVAC clinical trials

Note on Biologic Patents

Matching patents to biologic drugs is far more complicated than for small-molecule drugs.

DrugPatentWatch employs three methods to identify biologic patents:

  1. Brand-side disclosures in response to biosimilar applications
  2. These patents were identified from disclosures by the brand-side company, in response to a potential biosimilar seeking to launch. They have a high certainty of blocking biosimilar entry. The expiration dates listed are not estimates — they're expiration dates as indicated by the brand-side company.

  3. General brand-side disclosures
  4. These patents were identified from searching drug labels and other general disclosures from the brand-side company. This list may exclude some of the patents which block biosimilar launch, and some of these patents listed may not actually block biosimilar launch. The expiration dates listed for these patents are estimates, based on the grant date of the patent.

  5. Patents from broad patent text search
  6. For completeness, these patents were identified by searching the patent literature for mentions of the branded or ingredient name of the drug. Some of these patents protect the original drug, whereas others may protect follow-on inventions or even inventions casually mentioning the drug. The expiration dates listed for these patents are estimates, based on the grant date of the patent.

1) High Certainty: US Patents for TICOVAC Derived from Brand-Side Litigation

No patents found based on brand-side litigation

2) High Certainty: US Patents for TICOVAC Derived from Company Disclosures

No patents found based on company disclosures

3) Low Certainty: US Patents for TICOVAC Derived from Patent Text Search

No patents found based on company disclosures

TICOVAC Market Analysis and Financial Projection

Market Dynamics and Financial Trajectory for TICOVAC

Introduction to TICOVAC

TICOVAC™, developed by Pfizer, is the first and only FDA-approved vaccine in the United States designed to protect against Tick-Borne Encephalitis (TBE) for adults and children. This vaccine marks a significant milestone in the prevention of TBE, a serious and potentially fatal disease prevalent in certain regions of Europe and Asia.

Market Need and Growth Drivers

Increasing Prevalence of TBE

The global Tick-Borne Encephalitis Vaccine Market is driven by the increasing prevalence of TBE, particularly in Europe and Asia. Several thousand cases are reported annually, with many more likely going unreported. This rising incidence is a key factor driving the demand for TBE vaccines[4].

Geographical Distribution

The market is segmented geographically, with North America and Europe holding significant shares due to well-developed healthcare infrastructure and government support. The European TBE virus accounts for the largest segment by virus type, and this region is expected to maintain its lead during the forecast period[4].

End-User Segmentation

The market is also segmented by end-user, with traveler vaccines being the major segment. High-risk activities such as working or camping in forested areas, adventure travel, or living in TBE-endemic areas for extended periods contribute to the growth of this segment[4].

Regulatory Approval and Commercial Success

FDA Approval

TICOVAC™ received FDA approval in August 2021, marking a crucial step in its commercial journey. This approval is significant for Pfizer, as it expands the company's vaccine portfolio and addresses a critical public health need[1].

Commercial Success Uncertainties

Despite the regulatory approval, there are uncertainties regarding the commercial success of TICOVAC™. Factors such as the ability to meet clinical endpoints, regulatory submissions, and launch dates can impact its market performance. Additionally, the satisfaction of regulatory authorities with clinical study designs and results, as well as the determination of the product’s benefits versus risks, are critical for its commercial viability[1].

Financial Performance and Projections

Pfizer's Overall Financial Context

Pfizer's financial performance in recent years has been significantly influenced by its COVID-19 related products, Comirnaty and Paxlovid. However, with the decline in revenues from these products, the company is focusing on other segments, including vaccines like TICOVAC™. In 2023, Pfizer reported full-year revenues of $58.5 billion, a 42% decrease from 2022, primarily due to the decline in Comirnaty and Paxlovid revenues. Excluding these contributions, Pfizer's revenues grew 7% operationally[2].

Revenue Potential of TICOVAC

While specific revenue figures for TICOVAC™ are not detailed in Pfizer's financial reports, the vaccine is part of the broader biopharmaceutical segment that has shown operational growth. The launch of new products and indications, including TICOVAC™, contributes to this growth. For instance, other new products like Abrysvo have contributed significantly to Pfizer's revenues, indicating potential for similar contributions from TICOVAC™[2].

Market Size and Forecast

Global TBE Vaccine Market

The global Tick-Borne Encephalitis Vaccine Market was valued at USD 3272.5 million in 2021 and is projected to reach USD 5018.9 million by 2030, growing at a CAGR of 6.3% from 2023 to 2030. This growth is driven by increasing awareness, emerging healthcare infrastructure, and government funding in various regions[4].

Challenges and Restraints

High Cost of Vaccines

One of the major restraints for the TBE vaccine market is the high cost of vaccines, which makes them unaffordable for many in emerging economies. This cost barrier can limit the market's potential growth and penetration in these regions[4].

Competitive Landscape

The competitive landscape of the TBE vaccine market involves several key players, with Pfizer being a significant entrant. The market attractiveness and competitive positioning of these players are influenced by factors such as service features, innovations, scalability, and industry reach. Companies are ranked into categories like Active, Cutting Edge, Emerging, and Innovators based on these factors[4].

Strategic Implications

Research and Development

Pfizer's investment in research and development is crucial for the success of TICOVAC™. The company's R&D expenses have increased significantly, driven by investments in late-stage clinical programs and collaborations with other companies. This ongoing R&D effort is essential for addressing any emerging challenges and ensuring the vaccine's efficacy and safety[3].

Government and Public Health Support

Government funding and public health recommendations play a vital role in the adoption and commercial success of vaccines like TICOVAC™. Pfizer faces uncertainties regarding the recommendations from vaccine technical committees and other public health authorities, which can impact the vaccine's market potential[1].

Key Takeaways

  • Regulatory Milestone: TICOVAC™ is the first FDA-approved vaccine for TBE in the U.S., marking a significant regulatory achievement.
  • Market Growth: The global TBE vaccine market is projected to grow at a CAGR of 6.3% from 2023 to 2030, driven by increasing prevalence and awareness.
  • Financial Potential: While specific revenue figures for TICOVAC™ are not detailed, it contributes to Pfizer's operational revenue growth in the biopharmaceutical segment.
  • Challenges: High vaccine costs and regulatory uncertainties are key challenges that need to be addressed.
  • Strategic Focus: Continued investment in R&D and support from government and public health authorities are crucial for the vaccine's success.

FAQs

What is TICOVAC™?

TICOVAC™ is the first FDA-approved vaccine in the U.S. designed to protect against Tick-Borne Encephalitis (TBE) for adults and children.

What are the key drivers of the TBE vaccine market?

The key drivers include the increasing prevalence of TBE, especially in Europe and Asia, and the growing awareness and healthcare infrastructure in these regions.

What are the main challenges facing the TBE vaccine market?

The high cost of vaccines and regulatory uncertainties are significant challenges that could hinder market growth.

How does TICOVAC™ fit into Pfizer's financial strategy?

TICOVAC™ is part of Pfizer's broader strategy to diversify its product portfolio beyond COVID-19 related products and to drive operational revenue growth in the biopharmaceutical segment.

What is the projected market size for the TBE vaccine market by 2030?

The global TBE vaccine market is projected to reach USD 5018.9 million by 2030, growing at a CAGR of 6.3% from 2023 to 2030.

Cited Sources

  1. U.S. FDA Approves TICOVAC™, Pfizer's Tick-Borne Encephalitis Vaccine - Pfizer Press Release.
  2. Pfizer Reports Full-Year 2023 Results and Reaffirms Full-Year 2024 Guidance - Pfizer Earnings Release.
  3. Pfizer Reports Fourth-Quarter and Full-Year 2021 Results - Pfizer Earnings Release.
  4. Tick-borne Encephalitis Vaccine Market Size, Share, Trends and Forecast - Verified Market Research.

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