United States Toxoid Vaccine Market Demand & Supply Dynamics | Access Detailed Market Data - Serum Institute of India Pvt. Ltd., Bio Farma, Biological E, Panacea Biotec, Walvax Biotechnology Co., Ltd

global toxoid vaccine market reached US$ 5,634.84 Million in 2024 and is expected to reach US$ 8,850.18 Million by 2033, growing at a CAGR of 5.8 % during the forecast period of 2025-2033.

United States Toxoid Vaccine Market size in 2024: USD 2.1 B and projection to USD 3.3 B by 2032 with a CAGR 5.8% (2025-2032)

Japan Toxoid Vaccine Market size in 2024: USD 0.46 B and projection to USD 0.62 B by 2032 with a CAGR 3.7% (2025-2032)

DataM Intelligence has published a new research report on "Toxoid Vaccine Market Size 2025". The report explores comprehensive and insightful Information about various key factors like Regional Growth, Segmentation, CAGR, Business Revenue Status of Top Key Players and Drivers. The purpose of this report is to provide a telescopic view of the current market size by value and volume, opportunities, and development status.

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Latest M&A Activity

The toxoid vaccine sector remains concentrated with key players like GlaxoSmithKline, Sanofi Pasteur, Pfizer, and Merck leading vaccine development and distribution. There has been moderate M&A activity as companies aim to expand geographic reach and vaccine portfolios, particularly in emerging markets.​

Bharat Biotech and Shenzhen Kangtai Biological Products are emerging regional players challenging established multinationals in vaccine production and distribution, particularly targeting toxoid vaccines for diphtheria, tetanus, and pertussis

Key Players:

Sanofi, GSK plc, Merck/Sanofi Pasteur (MSP), Serum Institute of India Pvt. Ltd., Bio Farma, Biological E, Panacea Biotec, Walvax Biotechnology Co., Ltd., Bharat Biotech., MassBiologics, and Mitsubishi Tanabe Pharma Corporation

Key Development:

In December 2024, LimmaTech Biologics AG, a clinical-stage biotechnology company, announced that the U.S. FDA had granted Fast Track designation to its multivalent toxoid vaccine candidate, LBT-SA7. The vaccine is designed to prevent skin and soft tissue infections (SSTIs) caused by the bacterium Staphylococcus aureus (S. aureus).

Growth Forecast Projected:

The Global Toxoid Vaccine Market is anticipated to rise at a considerable rate during the forecast period, between 2025 and 2032. In 2024, the market is growing at a steady rate, and with the rising adoption of strategies by key players, the market is expected to rise over the projected horizon.

Research Process:

Both primary and secondary data sources have been used in the global Toxoid Vaccine Market research report. During the research process, a wide range of industry-affecting factors are examined, including governmental regulations, market conditions, competitive levels, historical data, market situation, technological advancements, upcoming developments, in related businesses, as well as market volatility, prospects, potential barriers, and challenges.

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Key Segments:

By Disease Type: (Tetanus, Diphtheria, Pertussis, Botulism)

By Vaccine Type: (Diphtheria, Tetanus, and Pertussis (DtaP), Diphtheria and Tetanus (DT), Tetanus, Diphtheria, and Pertussis (Tdap), Monovalent Tetanus Toxoid (TT), Tetanus and Diphtheria (Td), Others)

By Age Group: (Neonates, Children, Adults, Others)

By End-User: (Hospitals and Clinics, Government Organizations, Others)

Recent Product Launches and Approvals

The U.S. FDA further endorsed existing toxoid vaccines such as BOOSTRIX® (GSK) and Adacel® (Sanofi) for booster immunization and maternal vaccination programs to protect infants against pertussis.​

Serum Institute of India launched SIIPL Tdap, a new tetanus toxoid vaccine approved in late 2024, with strong safety and immunogenicity profile demonstrated in Phase 1/III clinical trials, positioning it to support expanded immunization efforts in Asia.​

Combination vaccines such as pentavalent and hexavalent vaccines incorporating tetanus toxoid remain a focus for immunization programs aiming for broad pediatric protection covering multiple pathogens

Regional Analysis for Market:

⇥ North America (U.S., Canada, Mexico)

⇥ Europe (U.K., Italy, Germany, Russia, France, Spain, The Netherlands and Rest of Europe)

⇥ Asia-Pacific (India, Japan, China, South Korea, Australia, Indonesia Rest of Asia Pacific)

⇥ South America (Colombia, Brazil, Argentina, Rest of South America)

⇥ Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of Middle East & Africa)

Benefits of the Report:

Chapter 1: Sets the stage by outlining the report's coverage, summarizing key market segments by region, product type, and application. Presents a snapshot of market sizes, growth potential across segments, and anticipated industry evolution both short and long term.

Chapter 2: Highlights pivotal market insights and uncovers the most significant emerging trends driving change within the industry.

Chapter 3: Offers an in-depth look at the competitive landscape among Toxoid Vaccine producers, including revenue shares, strategic moves, and recent mergers and acquisitions.

Chapter 4: Presents comprehensive profiles of the market's key players, delving into details such as revenue, profit margins, product portfolios, and company milestones.

Chapters 5 & 6: Analyze Toxoid Vaccine revenue at both regional and country levels, providing quantitative breakdowns of market sizes, growth opportunities, and development prospects worldwide.

Chapter 7: Focuses on different market segments by type, examining their individual sizes and potential, guiding readers toward high-impact, untapped market areas.

Chapter 8: Explores segmentation by application, evaluating industry growth potential in various downstream markets and pinpointing promising sectors for expansion.

Chapter 9: Provides a thorough review of the industry's supply chain mapping out both upstream and downstream activities.

Chapter 10: Concludes with a summary of the report's key findings and highlights the most critical takeaways for industry stakeholders.

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Latest Clinical Trials

LimmaTech Biologics AG received FDA Fast Track designation for LBT-SA7, a multivalent toxoid vaccine candidate to prevent skin and soft tissue infections caused by multidrug-resistant Staphylococcus aureus, reflecting novel toxin-based vaccine development efforts.​

Multiple clinical trials continue apace to evaluate new formulations and boosting strategies to address pertussis resurgence and optimize immunity duration in adults and children

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