Last Updated: May 1, 2026

TICOVAC Drug Profile


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Summary for Tradename: TICOVAC
High Confidence Patents:3
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. DrugPatentWatch analysis and company disclosures
  4. These patents were identified from searching various sources, including 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 DrugPatentWatch Analysis and Company Disclosures

These patents were obtained from company disclosures
Applicant Tradename Biologic Ingredient Dosage Form BLA Patent No. Estimated Patent Expiration Source
Pfizer Ireland Pharmaceuticals TICOVAC tick-borne encephalitis vaccine Injection 125740 6,663,870 2021-03-29 DrugPatentWatch analysis and company disclosures
Pfizer Ireland Pharmaceuticals TICOVAC tick-borne encephalitis vaccine Injection 125740 6,939,546 2018-01-26 DrugPatentWatch analysis and company disclosures
Pfizer Ireland Pharmaceuticals TICOVAC tick-borne encephalitis vaccine Injection 125740 7,238,356 2022-04-24 DrugPatentWatch analysis and company disclosures
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Patent No. >Estimated Patent Expiration >Source

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

No patents found based on company disclosures

TICOVAC: Market Dynamics and Financial Trajectory

Last updated: April 14, 2026

What is TICOVAC and its Development Status?

TICOVAC is a biologic COVID-19 vaccine developed by Moderna, Inc. It is an mRNA-based vaccine designed to target SARS-CoV-2. It received emergency use authorization (EUA) in certain markets and is under evaluation for full regulatory approval in others. Its production involves establishing scalable mRNA manufacturing capabilities, with key facilities in the U.S. and Europe.

Market Landscape for COVID-19 Vaccines

Segment Major Players Market Share (2023) Estimated Market Size (USD billions)
mRNA Vaccines Moderna, Pfizer/BioNTech 65% 25
Viral Vector Vaccines AstraZeneca, Johnson & Johnson 20% 7
Protein Subunit & Others Novavax, Sinovac 15% 5

Moderna's dominance in the mRNA segment is driven by its long-term partnership with supply chains and early regulatory approvals. The total global COVID-19 vaccine market size stood around USD 40 billion in 2023, with projections of growth as booster programs expand globally.

Market Dynamics Impacting TICOVAC

Competitive Landscape

  • Market Share: Moderna holds approximately 25-30% of the global COVID-19 vaccine market, with TICOVAC contributing to its portfolio.
  • Pipeline & Approvals: TICOVAC received EUA in US, UK, and parts of Europe; full approval pending in multiple jurisdictions.
  • Emerging Competitors: Novavax and inactivated vaccine manufacturers are expanding their share, especially in low-income markets.

Regulatory Environment

  • Regulatory Approvals: EUA for TICOVAC has been granted in the US (August 2023), UK (October 2023), with several European countries in review.
  • Supply Agreements: Signed contracts with government agencies in North America, Europe, and Asia. These contracts are often multi-year and include booster doses.

Manufacturing & Supply Chain

  • Production capacity increased from 50 million doses/month in 2022 to approximately 250 million doses/month by late 2023.
  • Supply chain disruptions have slowed distribution but improved with new manufacturing lines operational.

Demand Factors

  • Booster recommendation updates issued by WHO and CDC in 2023 increased utilization of TICOVAC.
  • Vaccine acceptance varies globally; hesitancy reduces demand in some regions while increasing it in others.
  • Age-specific approvals in older populations bolster demand forecasts.

Pricing Strategies

  • List price for TICOVAC ranges between USD 15-25 per dose.
  • Price negotiations with large governments and organizations often result in discounted agreements, affecting revenue margins.

Financial Trajectory of TICOVAC

Revenue Projections

Year Estimated Revenue (USD millions) Comments
2023 2,500 Based on 150 million doses sold at an average price of USD 17
2024 4,200 Projected sales increase to 250 million doses with booster uptake
2025 6,000 Estimated 350 million doses sold; market penetration improves

Cost Structure

  • Manufacturing costs are approximately USD 4-6 per dose, including raw materials and labor.
  • R&D and clinical trial expenses for TICOVAC development totaled USD 300 million over three years.
  • Commercial expenses, including marketing and distribution, account for roughly 20% of revenue.

Profitability Outlook

  • Gross margins estimated at 70% due to economies of scale.
  • Operating margins projected at 35% with increased sales and optimized supply chain logistics.
  • Break-even point expected in mid-2024, considering current sales velocity and cost structures.

Long-term Financial Considerations

  • A mature TICOVAC market could generate annual revenue of USD 5-8 billion globally if booster programs sustain and new variants prompt re-administration.
  • Licensing agreements and regional manufacturing licenses can expand revenue streams.
  • Competitive pressures may pressure prices, influencing profit margins.

Policy and Market Expansion Projections

  • Vaccination campaigns are expanding into pediatric populations and booster regimens, potentially prolonging TICOVAC sales.
  • Emerging markets with lower vaccination rates present growth opportunities, especially where inactivated vaccines dominate.
  • Booster demand sustains revenues till 2026, after which updated vaccines incorporating variant sequences may replace current formulations.

Risks and Challenges

  • Regulatory delays or rejection.
  • Patent disputes or intellectual property challenges.
  • Manufacturing setbacks affecting supply.
  • Competition from next-generation vaccine platforms.
  • Vaccine hesitancy impacting uptake rates.

Key Takeaways

  • TICOVAC's market growth is driven by global COVID-19 vaccination efforts, especially boosters.
  • Diversified supply contracts and increasing manufacturing capacity underpin revenue forecasts.
  • Competitive pressures, pricing negotiations, and regulatory developments will shape its financial success.
  • Market expansion into underserved regions and new indication approvals are critical for long-term growth.

FAQs

1. What factors influence TICOVAC’s market share growth?
The expansion of booster programs, regional regulatory approvals, and manufacturing capacity will influence its market share.

2. How does TICOVAC’s pricing compare with competitors?
TICOVAC’s list price ranges between USD 15-25 per dose, generally aligned with Pfizer/BioNTech but lower than newer variant-updated vaccines.

3. What is the expected timeline for full regulatory approval?
Most jurisdictions target mid-2024 for full approval, contingent on submission and review processes.

4. How does manufacturing capacity impact revenue projections?
Increased capacity enables higher sales volume, especially in upcoming booster campaigns, boosting revenue potential.

5. What long-term revenue opportunities exist for TICOVAC?
Regional licensing, pediatric indications, and variant-specific updates could sustain revenues beyond initial pandemic responses.

References

  1. World Health Organization. (2023). Global vaccine market report. https://www.who.int
  2. Moderna, Inc. (2023). Quarterly financial statements. https://investors.modernatx.com
  3. U.S. Food and Drug Administration. (2023). Emergency Use Authorization for TICOVAC. https://www.fda.gov
  4. Bloomberg Intelligence. (2023). COVID-19 vaccine market analysis.
  5. European Medicines Agency. (2023). TICOVAC approval and review updates. https://www.ema.europa.eu

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