Biosimilar Market Growth Revenue, Developments, Size, Share, and Forecast 2030

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Biosimilar Market size was valued at USD 24.86 Billion in 2023 and the total Biosimilars revenue is expected to grow at a CAGR of 17.02 % from 2024 to 2030, reaching nearly USD 74.70 Billion by 2030.

Biosimilar Market Poised to Reach USD 74.70 Billion by 2030

Patent expirations, rising healthcare costs, and demand for affordable treatments drive robust market growth.

Market Overview

The Biosimilar Market Growth, encompassing biologic drugs that are highly similar to approved reference biologics, was valued at USD 24.86 billion in 2023. Projections indicate a compound annual growth rate (CAGR) of 17.02%, with the market expected to reach approximately USD 74.70 billion by 2030.

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Market Dynamics

Several key factors contribute to this anticipated growth:

  • Patent Expirations: The expiration of patents for major biologic drugs has opened avenues for biosimilar entry. For instance, the patent expiry of Humira facilitated the introduction of biosimilars like Amgen's Amjevita and Pfizer's Abrilada, offering cost-effective alternatives for autoimmune conditions. 

  • Rising Healthcare Costs: Escalating healthcare expenses have intensified the demand for affordable treatment options. Biosimilars, such as Amgen's Kanjinti (trastuzumab) for breast cancer, provide lower-cost alternatives without compromising efficacy, thereby alleviating financial burdens on healthcare systems.

  • Increasing Incidence of Chronic Diseases: The growing prevalence of chronic conditions necessitates accessible and affordable therapies. Biosimilars address this need by offering comparable therapeutic benefits at reduced costs, enhancing patient access to essential treatments.

Market Challenges

Despite the positive outlook, the biosimilar market faces certain challenges:

  • Regulatory Hurdles: Navigating complex regulatory pathways for biosimilar approval can be time-consuming and costly, potentially delaying market entry.

  • Market Acceptance: Achieving acceptance among healthcare providers and patients requires demonstrating equivalence in efficacy and safety compared to reference biologics.

  • Intellectual Property Issues: Legal disputes over patents and exclusivity rights can impede the timely introduction of biosimilars.

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Market Segmentation

The biosimilar market is segmented based on product type and application:

  • By Product Type:

    • Monoclonal Antibodies: These biosimilars are widely used in treating various cancers and autoimmune diseases.

    • Erythropoietin: Utilized for anemia associated with chronic kidney disease and chemotherapy.

    • Granulocyte Colony-Stimulating Factor (G-CSF): Employed to prevent infections in patients undergoing chemotherapy.

    • Insulin: Biosimilar insulins provide affordable options for diabetes management.

    • Others: Including growth hormones and fertility hormones.

  • By Application:

    • Oncology: Biosimilars play a crucial role in cancer treatment by offering cost-effective therapeutic options.

    • Autoimmune Diseases: Conditions like rheumatoid arthritis and psoriasis benefit from biosimilar therapies.

    • Diabetes: Biosimilar insulins contribute to affordable diabetes care.

    • Blood Disorders: Treatments for anemia and neutropenia often involve biosimilars.

    • Others: Including growth hormone deficiencies and fertility issues.

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Regional Insights

  • North America: The United States leads the biosimilar market, driven by patent expirations of key biologics, supportive regulatory frameworks, and increasing adoption among healthcare providers.

  • Europe: Europe has been at the forefront of biosimilar approvals and adoption, with countries like Germany, France, and the UK exhibiting significant market shares due to well-established regulatory pathways and acceptance.

  • Asia-Pacific: Countries such as China, India, and South Korea are witnessing rapid market growth, attributed to increasing healthcare expenditures, a large patient population, and government initiatives promoting biosimilars.

Key Market Players

Prominent companies contributing to the biosimilar market include:

  • Pfizer Inc.: Offers a diverse biosimilar portfolio, including Ruxience (rituximab), expanding patient access to essential therapies.

  • Amgen Inc.: Developed Kanjinti (trastuzumab), addressing critical needs in breast cancer treatment.

  • Sandoz (Novartis): A leader in biosimilar development, providing a range of therapies across various indications.

  • Biocon Ltd.: Engages in strategic alliances, such as the partnership with Mylan, to advance biosimilar developments and expand market reach.

  • Celltrion Healthcare: Known for its biosimilar offerings in autoimmune diseases and oncology.

Conclusion

The global biosimilar market is on a robust growth trajectory, fueled by patent expirations, escalating healthcare costs, and the increasing prevalence of chronic diseases. While challenges like regulatory complexities and market acceptance persist, ongoing innovations, strategic collaborations, and supportive policies are expected to enhance patient access to affordable and effective treatments. Stakeholders, including healthcare providers, policymakers, and industry players, must collaborate to navigate these challenges and harness the full potential of biosimilars in improving global health outcomes.

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