시장보고서
상품코드
1820369

생물제제 시장 규모, 점유율, 동향, 예측 : 공급원별, 제품별, 질환별, 제조별, 지역별(2025-2033년)

Biologics Market Size, Share, Trends and Forecast by Source, Product, Disease, Manufacturing, and Region, 2025-2033

발행일: | 리서치사: IMARC | 페이지 정보: 영문 135 Pages | 배송안내 : 2-3일 (영업일 기준)

    
    
    




※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

세계 생물제제 시장 규모는 2024년 3,776억 달러에 달했습니다. IMARC Group은 2033년에는 7,697억 달러에 달하고, 2025-2033년 7.38%의 연평균 복합 성장률(CAGR)을 보일 것으로 예측했습니다. 현재 북미가 시장을 독점하고 있으며, 2024년 시장 점유율은 44.8%를 초과할 것으로 예측됩니다. 보다 효과적인 치료 옵션이 필요한 만성 질환의 유병률 증가, 보다 표적화된 치료법 개발을 촉진하는 지속적인 기술 발전, 첨단 약물 전달 시스템의 출현은 생물제제 시장 점유율을 촉진하는 요인 중 일부입니다.

세계 바이오의약품 시장은 혁신적인 치료법과 바이오테크놀러지의 발전에 대한 수요 증가로 인해 매우 빠른 속도로 성장하고 있습니다. 생물학적제제란 생물체에서 유래한 제품으로, 단일클론항체, 백신, 세포-유전자치료제, 유전자치료제, 재조합단백질 등이 포함됩니다. 이 모든 치료법은 당뇨병, 암, 자가면역질환과 같은 만성질환에 대한 집중적이고 효과적인 치료를 가져와 의료계에 변화를 가져오고 있습니다. 만성질환 유병률 증가는 노인 인구 증가와 함께 생물제제의 보급을 크게 부추기고 있습니다. 또한, 연구개발에 대한 투자로 비용 효율적인 대안이 될 수 있는 바이오시밀러를 포함한 차세대 바이오의약품의 출시가 빠르게 진행되고 있습니다. 규제와 승인에 의한 지원도 생물제제 시장 성장의 길을 열어주고 있습니다.

미국은 생물제제의 주요 지역 시장으로 부상하고 있습니다. 이 시장은 혁신적인 치료법에 대한 수요 증가, 생명공학의 발전, 개인 맞춤형 의료에 대한 관심 증가로 인해 활성화되고 있습니다. 암, 자가면역질환, 당뇨병 등 만성질환의 높은 유병률이 생물학적 치료제 수요를 견인하고 있습니다. 바이오시밀러의 확대와 기존 의약품보다 생물제제를 사용하는 경향은 시장 성장에 더욱 박차를 가하고 있습니다. 생물제제 시장 분석 보고서에 따르면, 제약 기업의 꾸준한 연구개발 투자 확대와 정부의 우호적인 정책이 시장 성장을 가속하고 있습니다. 또한, 의료 인프라 구축과 상환 정책은 생물제제의 가용성을 더욱 높이고 있습니다. 또한, 정밀의료에 대한 관심과 생물제제의 미래가 미국 시장의 안정적 성장을 견인할 것입니다.

생물제제 시장 동향

표적 치료의 끊임없는 혁신

복잡한 분자에 대한 생물제제의 중요한 시장 동향 중 하나는 표적치료제의 끊임없는 혁신입니다. 이는 질병의 원인이 되는 특정 세포나 분자에 특이적으로 작용하도록 설계된 치료법으로, 부작용을 최소화하면서 치료 효과를 높일 수 있습니다. 암이나 자가면역질환과 같은 질병의 심각한 특성을 고려할 때, 표적치료제는 새롭고 효과적인 치료 수단을 제공합니다. 유럽종양학회에 따르면, 2006-2020년 사이 18개 암종에서 36개 유전체 적응증을 타겟으로 하는 51개 약물이 72건 승인되었고, 유전체 표적 치료의 적격성은 5.13%에서 13.60%로 증가했으며, 반응률은 2.73%에서 7.04%로 상승하였습니다. 반면, 유전체 정보 기반 치료법은 적격성을 10.70%에서 27.30%로 증가시켰고, 반응률은 3.33%에서 11.10%로 개선되었습니다. 예를 들어, 2024년 3월 캘리포니아 공대 연구진은 부작용을 최소화한 암 치료에 초점을 맞춘 초음파 활성화 약물 전달 시스템을 개발했습니다. 이 기술은 가스 소포와 메카노포어를 결합하여 약물을 활성화시켜 건강한 조직에 대한 해를 정확하게 감소시키는 기술입니다. 마찬가지로 2024년 3월 Nature Medicine지에는 상피세포성장인자수용체(EGFR)와 인터루킨13수용체α2(IL13Ra2) 두 가지 단백질을 이중 표적으로 하는 2가 키메라 항원수용체 T세포(자가세포)를 재발성 교모세포종(rGBM) 환자에게 피내투여한 결과를 발표하였습니다. 이 표적 T세포는 공격적인 뇌종양의 성장 종말에 대항합니다. 대규모 연구를 통해 분자 수준에서 질병의 메커니즘이 밝혀졌고, 그 결과 기존 접근법보다 훨씬 더 효과적이고 독성이 적은 특수 치료법을 제공하게 되었습니다. 이러한 추세는 맞춤형 의료에 대한 관심 증가와 함께 연구개발에 대한 투자를 증가시킬 것으로 보입니다. 그 도입과 그 이후의 성공은 복잡한 분자에 대한 수요를 크게 증가시켜 시장에 중요한 촉매제 역할을 할 것입니다. 더 높은 효과와 낮은 독성을 제공하는 정밀치료에 대한 관심이 높아짐에 따라 표적 생물제제에 대한 시장 수요가 가속화되고 있습니다.

첨단 약물 전달 시스템의 등장

약물 전달 시스템은 헬스케어에서 점점 더 중요해지고 있으며, 복잡한 분자 치료의 효과와 환자의 순응도를 좌우하기도 합니다. 이 분야의 기술 혁신은 방출 제어 메커니즘부터 나노기술에 기반한 전달 시스템까지 다양한 형태로 이루어지고 있습니다. 보고서에 따르면, 나노기술은 2024년까지 전 세계적으로 1,250억 달러를 넘어설 것으로 예상되며, 표적 약물 전달을 촉진하고, 암 치료를 촉진하고, 생체 분자의 안정성과 효능을 향상시킴으로써 생물제제를 변화시킬 것으로 예측됩니다. 2024년 1월, 노스캐롤라이나 대학의 과학자들이 반창고와 같은 무선 약물 전달 시스템인 'Spatiotemporal On-Demand Patch SOP'를 발표한 것이 그 한 예다. 이 무선 패치는 컴퓨터나 스마트폰에서 지령을 받아 마이크로니들에서 약물 전달을 스케줄링하고 제어할 수 있는 무선 패치입니다. 이를 통해 환자는 보다 쉽게 치료 계획을 따를 수 있으며, 임상 현장에서 더 나은 결과를 얻을 수 있습니다. 새로운 전달 시스템은 궁극적으로 매일 주사를 주 1회 또는월1회 투여로 대체하여 환자의 편의성과 치료 지속 의지를 크게 향상시킬 수 있습니다. 복잡한 분자의 치료 효율을 극대화하기 위해 연구 개발에 많은 투자가 이루어지고 있습니다. 이러한 약물 전달 시스템 연구는 보다 효율적이고 환자 친화적인 대체 치료제에 대한 큰 수요를 충족시키는 데 있어 생물제제 시장 가치와 성장 기회에 크게 기여하고 있습니다. 이러한 혁신 중심의 환경은 환자 중심의 치료 모델에 따른 전달 방식에 대한 수요 증가를 반영하고 있습니다.

규제 변화와 조화

헬스케어 업계 기업들은 매우 어렵고 복잡한 규제 환경에 대처해야 했습니다. 그러나 규제 조화로 인해 시나리오는 점점 더 단순화되고 있습니다. 미국 식품의약국(FDA)이 2023년 7월 발표한 '의약품 임상시험 실시기준(GCP) E6(R3)'은 국제임상시험적합성위원회(ICH)의 협력 하에 '보다 혁신적이고 효율적인 임상시험 설계를 강화하기 위해 ICH 회원국 및 지역 간 임상 데이터의 상호 수용을 촉진하는 상호 수용을 촉진하는 통일된 기준을 제공하는 것"을 목적으로 하고 있습니다. 국가 간 통일된 또는 상호 인정된 승인 절차로 인해 시장 진입 장벽이 크게 낮아진 것은 새로운 제품이나 기존 제품이 이전보다 훨씬 더 빨리, 더 많은 환자들에게 더 쉽게 도달할 수 있다는 것을 의미합니다. 혁신적인 치료법을 환자들에게 신속하게 적용하고 그 지리적 범위를 크게 확대하는 것은 중요한 의미를 갖습니다. 승인 획득을 가속화하고 시장 접근성을 확대하는 이러한 약사 규제 정합성은 복잡한 생물제제 분자 세계 시장의 지속적인 성장을 가속하고 생물제제 시장의 긍정적인 전망을 창출하고 있습니다. 이러한 규제 합리화 노력은 전 세계 제조업체들이 국경을 초월한 생물제제 개발에 더 적극적으로 투자하도록 유도하고 있습니다.

목차

제1장 서문

제2장 조사 범위와 조사 방법

  • 조사 목적
  • 이해관계자
  • 데이터 소스
    • 1차 정보
    • 2차 정보
  • 시장 추정
    • 보텀업 접근
    • 톱다운 접근
  • 조사 방법

제3장 주요 요약

제4장 서론

제5장 세계의 생물제제 시장

  • 시장 개요
  • 시장 실적
  • COVID-19의 영향
  • 시장 예측

제6장 시장 분석 : 공급원별

  • 미생물
  • 포유류
  • 기타

제7장 시장 분석 : 제품별

  • 단일클론항체
  • 백신
  • 재조합 단백질
  • 안티센스, RNAi 및 분자 요법
  • 기타

제8장 시장 분석 : 질환별

  • 종양
  • 면역 질환
  • 심혈관 질환
  • 혈액 질환
  • 기타

제9장 시장 분석 : 제조별

  • 아웃소싱
  • 사내

제10장 시장 분석 : 지역별

  • 북미
    • 미국
    • 캐나다
  • 아시아태평양
    • 중국
    • 일본
    • 인도
    • 한국
    • 호주
    • 인도네시아
    • 기타
  • 유럽
    • 독일
    • 프랑스
    • 영국
    • 이탈리아
    • 스페인
    • 러시아
    • 기타
  • 라틴아메리카
    • 브라질
    • 멕시코
    • 기타
  • 중동 및 아프리카

제11장 SWOT 분석

제12장 밸류체인 분석

제13장 Porter의 Five Forces 분석

제14장 가격 분석

제15장 경쟁 구도

  • 시장 구조
  • 주요 기업
  • 주요 기업 개요
    • AbbVie Inc.
    • Amgen Inc.
    • AstraZeneca plc
    • F. Hoffmann-La Roche Ltd
    • GlaxoSmithKline plc
    • Johnson & Johnson
    • Merck KGaA
    • Novartis AG
    • Pfizer Inc.
    • Sanofi
LSH 25.10.13

The global biologics market size was valued at USD 377.6 Billion in 2024. Looking forward, IMARC Group estimates the market to reach USD 769.7 Billion by 2033, exhibiting a CAGR of 7.38% from 2025-2033. North America currently dominates the market, holding a market share of over 44.8% in 2024. The rising prevalence of chronic diseases, which necessitate more effective treatment options, continuous technological advancements facilitating the development of increasingly targeted therapies, and the emergence of advanced drug delivery systems are some of the factors catalyzing the biologics market share.

The global biologics market is expanding at a very fast pace due to the increasing demand for innovative therapies and biotechnology advancement. Biologics are products that derive from living organisms, and such products include monoclonal antibodies, vaccines, cell and gene therapies, and recombinant proteins. All of these therapies are altering health care since they bring focused, effective treatments for chronic diseases such as diabetes, cancer and autoimmune diseases. The increasing incidence of chronic diseases, along with the geriatric population, is highly driving the uptake of biologics. Furthermore, investments in research and development are fast-tracking the launch of next-generation biologics, including biosimilars, which provide cost-effective alternatives. Support from regulations and approvals has also paved the way for the biologics market growth.

The United States has emerged as a key regional market for biologics. The market is fueled by growing demand for innovative therapies, advancements in biotechnology, and increasingly interested in personalized medicine. The high incidence of chronic conditions, such as cancer, autoimmunity disorders, and diabetes, is driving the demand for biological treatments. The further expansion of biosimilars and the trend toward more use of biologic medicines over traditional pharmaceuticals is fueling further market growth. As per the biologics market analysis report, steadily growing investment research and development by pharmaceutical companies in support of favorable government policies promote growth in the market. Moreover, improvement in infrastructure for healthcare and reimbursement policy further enhances the availability of biological drugs. Further, a focus on precision medicine and the future of biologics is going to help the U.S. market grow steadily.

Biologics Market Trends:

Continuous innovations in targeted therapies

One of the significant biologics market trends for complex molecules is the continuous innovation in targeted therapies. These are therapies designed to specifically act on certain cells or molecules responsible for disease, thus increasing treatment effectiveness while minimizing side effects. Given the critical nature of diseases like cancer and autoimmune disorders, targeted therapies offer a novel and effective avenue for treatment. According to the European Society for Medical Oncology, between 2006 and 2020, there were 72 approvals for 51 drugs targeting 36 genomic indications across 18 types of cancer, which increased eligibility for genome-targeted therapies from 5. 13% to 13. 60% and increased response rates from 2. 73% to 7. 04%. Meanwhile, genome-informed therapies increased eligibility from 10. 70% to 27. 30% and response rates improved from 3. 33% to 11. 10%. For example, in March 2024, Caltech researchers created an ultrasound-activated drug-delivery system that focused on cancer treatment with minimum side effects. This technique combines gas vesicles and mechanophores to activate drugs, thereby reducing harm to healthy tissues precisely. Similarly, Nature Medicine released its report in March 2024 on the results of patients with recurrent glioblastoma (rGBM) treated intrathecally with bivalent chimeric antigen receptor T-cells, being autologous, with dual targeting of two proteins: epidermal growth factor receptor (EGFR), interleukin-13 receptor alpha 2 (IL13Ra2). These targeted T-cells against aggressive brain tumor growth end. Science research in large scales has been able to reveal mechanisms of diseases at the molecular level, and thus a treatment approach has been provided with specialized therapies that are much more effective and less toxic than traditional approaches. This trend is likely to see increased investments in research and development, along with a heightened focus on personalized medicine. Their introduction and subsequent success can significantly increase the demand for complex molecules, thereby acting as a critical catalyst for the market. The rising preference for precision treatments that offer higher efficacy and lower toxicity is accelerating market demand for targeted biologics.

Emergence of advanced drug delivery systems

Drug delivery systems have become increasingly important in healthcare, often determining the efficacy and patient compliance for complex molecular treatments. Innovation in this field takes many forms, from controlled-release mechanisms to nanotechnology-based delivery systems. According to reports, nanotechnology is expected to cross USD 125 Billion worldwide by 2024, which transforms biologics by facilitating targeted drug delivery, boosting cancer therapies, and increasing the stability and effectiveness of biomolecules. An example includes scientists from the University of North Carolina, who, in January 2024, launched the Spatiotemporal On-Demand Patch SOP, a wireless drug delivery system that resembles a band-aid. The wireless patch can receive commands from the computer or smartphone, where its delivery can be scheduled and controlled on the microneedle. This will allow a patient to follow the plan for their treatment much easier, leading to better outcomes in clinical practice. New delivery systems might eventually replace daily injections with a weekly or even a monthly dose, significantly increasing patient convenience and willingness to stay on treatment. Major investments are pouring into their research and development with the intention of maximizing the therapeutic efficiency of complex molecules. Such research in drug delivery systems advances significantly contribute to the biologics market value and opportunities for growth in satisfying a huge demand for more efficient, patient-friendly therapeutic alternatives. This innovation-driven environment reflects growing demand for delivery methods that align with patient-centric care models.

Regulatory changes and harmonization

Companies in the healthcare industry have had to grapple with a very difficult, labyrinthine regulatory environment. However, regulatory harmonization is making the scenario increasingly straightforward. The draft guidance of July 2023 from the US Food and Drug Administration, titled "Good Clinical Practice (GCP) E6(R3)", in cooperation with the International Council for Harmonisation (ICH), says it has been put in place "to provide a unified standard to facilitate mutual acceptance of clinical data between ICH member countries and regions in order to enhance more innovative and efficient design of clinical trials.". Reduced substantially, market entry barriers through unified or mutually recognized approval processes across different countries mean new and existing products can now easily reach a much wider patient base much sooner than they previously could. The rapid rollout of innovative therapies to patients and their significant geographic expansion has significant implications. This favorable alignment of regulatory practices, which expedites approval and expands market access, is driving ongoing growth in the global market for complex biologics molecules, thereby creating a positive biologics market outlook. These regulatory streamlining efforts are also encouraging global manufacturers to invest more aggressively in cross-border biologics development.

Biologics Industry Segmentation:

Analysis by Source:

  • Microbial
  • Mammalian
  • Others

The microbial sources account for a majority share of 58.5% driven mainly by their cost-effectiveness, scalability, and high productivity in biologics manufacture. Microorganisms such as E. coli and yeast are very widespread to produce recombinant proteins, enzymes, and vaccines because they produce at very fast growth rates and because of simpler genetic manipulation. The manufacture of biologics involving minimal post-translational modification is very good with the system, and therefore, they dominate insulin, growth hormones, and certain therapeutic enzymes. Advances in the technological aspects of fermentation systems and bioprocessing techniques have further increased yield and efficiency, thus making microbial platforms even more attractive. Increasing demand for biosimilars and the trend of precision medicine continue to fuel investment in microbial technologies. Pharmaceutical companies also prefer microbial systems as they help them meet regulatory compliance while lowering production costs. These factors will ensure the continued dominance of microbial platforms in biologics manufacturing.

Analysis by Product:

  • Monoclonal Antibodies
  • Vaccines
  • Recombinant Proteins
  • Antisense, RNAi, and Molecular Therapy
  • Others

Monoclonal antibodies represent the largest segment with a share of 66.7% due to their crucial role in cancer, autoimmune diseases, and infectious disorders. The accuracy in the specificity of targeting antigens has placed them in a position as indispensable in personalized medicine. New areas of improvement in antibody engineering include bispecific antibodies and antibody-drug conjugates, which improve the efficacy of the therapeutic products. More investments in R&D have accelerated the regulatory approvals of these products, and they are increasingly being applied in clinical practice. The growing adoption of biosimilar monoclonal antibodies offers cost-effective solutions, widening their accessibility and further fueling market expansion. With ongoing innovation and the rising prevalence of chronic diseases, monoclonal antibodies remain a cornerstone of biologics development and commercialization, ensuring sustained growth.

Analysis by Disease:

  • Oncology
  • Immunological Disorders
  • Cardiovascular Disorders
  • Hematological Disorders
  • Others

The oncology segment holds the largest share of 28.7%, supported by a global rise in cancer prevalence and the increasing adoption of targeted therapies. Advances in biologic products such as monoclonal antibodies, checkpoint inhibitors, and cell-based therapies offer improved survival advantages and quality of life as a part of cancer care. Investment in precision medicines and innovative developments in immuno-therapies also augment growth in this space. Further regulatory approval of new biologic products for varied types of cancers drives demand and supports growth in this market. As biologics demonstrate efficacy in managing and perhaps even curing cancers, their application within oncology remains on track, making it the most profitable segment in the market for biologics.

Analysis by Manufacturing:

  • Outsourced
  • In-House

In-house manufacturing leads the market with an 84.8% share, driven by the need to have greater control over production processes, intellectual property protection, and regulatory standards that are quite stringent. Companies using the in-house capacity can directly control quality assurance, respond quicker to production problems, and maintain integration with internal R&D teams. This also contributes to cost optimization in the long run by eliminating dependency on other partners. Such capability to streamline operations with proprietary knowledge, especially about high-value biologics, gives the advantage to in-house manufacturing. More importantly, modular and continuous manufacturing technologies have advanced with which companies have developed means to enhance scalability as well as efficiency, where different production demands can be met accordingly, but they do not have any external dependence on partners.

Regional Analysis:

  • North America
    • United States
    • Canada
  • Asia Pacific
    • China
    • Japan
    • India
    • South Korea
    • Australia
    • Indonesia
    • Others
  • Europe
    • Germany
    • France
    • United Kingdom
    • Italy
    • Spain
    • Russia
    • Others
  • Latin America
    • Brazil
    • Mexico
    • Others
  • Middle East and Africa

North America held the highest share in 2024, with over 44.8%. North America dominates the market due to its developed healthcare infrastructure and increased investments in biopharmaceutical research. It contains numerous top biopharmaceutical companies and research organizations. Such innovation by various entities in the region creates an optimistic outlook for the market. Favorable regulatory support in the form of fast-track approvals for biologics and various financial incentives for extensive research and development activities are also contributing to the market growth. Furthermore, increasing patient awareness and willingness to adopt new therapies are further fueling the demand for biologics in North America. The U.S. also constitutes the biggest market in the region, primarily due to high healthcare spending, broad insurance coverage, and increasing chronic and lifestyle-related diseases.

Advanced demand for biologic therapies, accelerating healthcare, and improving infrastructure for healthcare drive the Asia Pacific biologics market. The increasing prevalence of chronic diseases coupled with an increased awareness about, and affordability of, biologics is promoting growth in the market. Government incentives to develop biosimilars are also driving market growth and have surged healthcare expenditure in the nations of China and India. A huge patient population and increasing research and development are two of the primary drivers of this market growth in the region.

In Europe, a well-developed healthcare system with higher accessibility toward advanced biologic treatment enhances the market growth for biologics. A high rate of incidence of autoimmune diseases, cancer, and other chronic conditions stimulates the need for biologics. Governments' support with positive regulation sets an impetus to accept biosimilars. The region's focus on research and innovation with a strong healthcare infrastructure provides the right environment to grow in biologics. In addition, increased expenditure on healthcare, as well as collaborative efforts between the public and private sectors, contribute to the momentum of this market.

In Latin America, better access to healthcare is fueling the growth of biologics. The region is also witnessing increased investments in the healthcare sector and a greater prevalence of chronic diseases. Affordability and access to biologics are improving through the efforts of governments, thereby increasing demand. Biosimilar adoption is also increasing along with regional initiatives that help cut drug costs. Brazil, Mexico, and Argentina are some of the major contributors to this growth due to increasing awareness about biologics and the expansion of healthcare markets, which attracts investments from multinational pharmaceutical companies.

The biologics market of the Middle East and Africa is expanding due to increasing health investments in the region, development in healthcare facilities, and greater demand for advanced therapies. More chronic diseases are being noticed in the region, including diabetic conditions, cardiovascular disease, and cancer, which is making the demand for these biologic drugs rise. The government is also investing in healthcare reforms to make access to biologics better, especially in countries like the UAE, Saudi Arabia, and South Africa. The use of biosimilars and health awareness among patients is also increasing market growth.

Key Regional Takeaways:

United States Biologics Market Analysis

In 2024, the United Sates accounts for 88.70% of the biologics market in North America. The adoption of advanced treatments is transforming medicine by offering more personalized treatment options in the US. Advanced therapies are now tailored to specific disease mechanisms and have resulted in outcomes that traditional methods often cannot achieve. According to HIPAA Journal, the average private healthcare spending in the U. S. is USD 11,197 per person annually (CMS, 2024), which reflects this growing trend toward personalized medicine. This movement opens high-technology avenues for biologics to satisfy a diversity of medical needs. Shifting focus toward personalized medicine has significantly improved the condition of people with chronic diseases. Innovation in R&D is bringing safer and more efficient next-generation therapies. The tie-up between service providers, who are the healthcare operators, and the biotech organizations is accelerating non-stop new technology interventions into treatment modules while ensuring an effective governance architecture that will ensure and continue to drive safety coupled with innovation. Furthermore, better support for patients is bridging the access gaps to advanced therapies and leads to better management of disease. These collaborations are sowing a rich healthcare future that continually pushes the limits of medical advancement.

Asia Pacific Biologics Market Analysis

Fast innovations in advanced medical technologies are altering the treatment paradigms and providing tailored strategies that are meeting unmet clinical needs. Initiatives in the expansion of capacity for production are making access more widespread, thus facilitating the reduction of barriers to healthcare services. Collaboration between local research institutes and international companies promotes knowledge sharing and, thus, the pace of innovation. Sensitization and training programs are significantly increasing the patient's understanding and embracing of new therapeutic interventions. Investment in the healthcare structure is opening opportunities for many, especially those in the urban areas, to have access to complex treatment modalities. According to the Ministry of Health and Family Welfare, the healthcare structure of India is aided by an increase in government health spending, reaching about USD 51 Billion in 2021-22, and an aim for public investment to increase to 2.5% of GDP by 2025, builds support for the biologics ecosystem by enhancing the ease of access to superior health facilities through initiatives like National Health Mission and Ayushman Bharat Health Infrastructure Mission. The introduction of low-cost biosimilars plays a vital role in ensuring the extension of innovative medicines, thereby ensuring diverse population groups benefit from medical innovation.

Europe Biologics Market Analysis

European countries are emerging as leaders in healthcare innovation, focusing on cutting-edge research and novel medical breakthroughs. With more financial investment in biotechnology and clinical trials, the way is now becoming smooth for effective treatment options for complex health problems. Accelerations in the pace of disease management research and development resulting from collaborations between academic institutes and pharmaceutical companies have paved the way for better services to patients. Huge coverage of insurance systems and reimbursement structures make specialist care accessible as well as affordable for most of the population. This is seen in Germany; according to Germany Visa, Germany has allocated approximately $521.5 Billion toward healthcare in 2021, with over 90% of its population falling under statutory health insurance. This extensive coverage leads to a higher life expectancy and allows for significant investments in biologics focused on conditions like cancer and cardiovascular diseases. Moreover, sustainability is also becoming a priority, with green manufacturing approaches on the rise. The cross-border sharing of clinical data also supports the adoption of more advanced medical practices, leading to better healthcare delivery throughout the region.

Latin America Biologics Market Analysis

Advances in therapy in the field have been based on meeting local needs with specific tailored solutions, ensuring wider suitability. A greater emphasis on research and development in specific therapeutic areas helps to bring about cost-effective breakthroughs without compromising efficacy. According to the International Trade Administration, U. S. Department of Commerce, Brazil is the largest healthcare market in Latin America, with 9.47% of its GDP allocated to healthcare (USD161 Billion), which strengthens strong research and development programs that improve biologics innovation. With 427,097 hospital beds and public-private partnerships, its focus on innovation, including vaccine manufacturing and therapeutic developments, provides extensive opportunities for biologics to address chronic illnesses and prepare for pandemics. Using the latest emerging technologies, the region is able to show excellent local production capabilities, which is necessary to increase availability. Moreover, cross-industry efforts directed toward increasing knowledge-sharing and skill development create an environment that fosters transformational improvements.

Middle East and Africa Biologics Market Analysis

Biologics are transforming the treatment landscapes as they have precision in targeting the disease mechanisms. These therapies allow for more effective and tailored interventions, particularly with complex conditions, as they focus on root causes rather than merely addressing symptoms. Their capacity to provide individualized treatments promotes better results and lower probabilities of adverse side effects, thus instilling trust among patients and health professionals. At the same time, the growing prevalence of cancer has created a demand for innovative therapies. According to the WHO, the surging cancer rates in the Arab World, with an anticipated 1.8-fold increase in incidence by 2030, underscore the escalating burden of disease. This surge presents a significant opportunity for biologics, offering advanced therapeutic solutions to confront the rising public health challenge. This shift is driven by increased awareness about early diagnosis and improved access to advanced medical treatments. With the emphasis on improving outcomes, the uptake of innovative therapies is gaining pace steadily, making it a very lively environment for enhancements in treatment protocols and patient care.

Competitive Landscape:

Increasing focus is on strategic collaborations, acquisitions, and research for improving their market positioning by players in the biologics market. They are also focusing on advancement in monoclonal antibodies, gene therapies, and cell-based therapies that have potential applications in dealing with the complexity of disease states, including cancer, autoimmune diseases, and many genetic conditions. Next-generation biologics, including bispecific antibodies and CAR-T therapies, are investments by companies to fill in unmet medical needs. Biosimilars, too, are aggressively being developed by various market players, which take advantage of patent expiries for blockbuster biologic drugs, making them cost-efficient alternatives for originators. Biologic manufacturing processes have also become optimized through advanced technologies like automation, AI, and machine learning to enhance efficiency and scalability. These strategies are expected to fuel market growth and innovation over the coming years.

The report provides a comprehensive analysis of the competitive landscape in the biologics market with detailed profiles of all major companies, including:

  • AbbVie Inc.
  • Amgen Inc.
  • AstraZeneca plc
  • F. Hoffmann-La Roche Ltd
  • GlaxoSmithKline plc
  • Johnson & Johnson
  • Merck KGaA
  • Novartis AG
  • Pfizer Inc.
  • Sanofi

Key Questions Answered in This Report

  • 1.How big is the biologics market?
  • 2.What is the future outlook of biologics market?
  • 3.What are the key factors driving the biologics market?
  • 4.Which region accounts for the largest biologics market share?
  • 5.Which are the leading companies in the global biologics market?

Table of Contents

1 Preface

2 Scope and Methodology

  • 2.1 Objectives of the Study
  • 2.2 Stakeholders
  • 2.3 Data Sources
    • 2.3.1 Primary Sources
    • 2.3.2 Secondary Sources
  • 2.4 Market Estimation
    • 2.4.1 Bottom-Up Approach
    • 2.4.2 Top-Down Approach
  • 2.5 Forecasting Methodology

3 Executive Summary

4 Introduction

  • 4.1 Overview
  • 4.2 Key Industry Trends

5 Global Biologics Market

  • 5.1 Market Overview
  • 5.2 Market Performance
  • 5.3 Impact of COVID-19
  • 5.4 Market Forecast

6 Market Breakup by Source

  • 6.1 Microbial
    • 6.1.1 Market Trends
    • 6.1.2 Market Forecast
  • 6.2 Mammalian
    • 6.2.1 Market Trends
    • 6.2.2 Market Forecast
  • 6.3 Others
    • 6.3.1 Market Trends
    • 6.3.2 Market Forecast

7 Market Breakup by Product

  • 7.1 Monoclonal Antibodies
    • 7.1.1 Market Trends
    • 7.1.2 Market Forecast
  • 7.2 Vaccines
    • 7.2.1 Market Trends
    • 7.2.2 Market Forecast
  • 7.3 Recombinant Proteins
    • 7.3.1 Market Trends
    • 7.3.2 Market Forecast
  • 7.4 Antisense, RNAi and Molecular Therapy
    • 7.4.1 Market Trends
    • 7.4.2 Market Forecast
  • 7.5 Others
    • 7.5.1 Market Trends
    • 7.5.2 Market Forecast

8 Market Breakup by Disease

  • 8.1 Oncology
    • 8.1.1 Market Trends
    • 8.1.2 Market Forecast
  • 8.2 Immunological Disorders
    • 8.2.1 Market Trends
    • 8.2.2 Market Forecast
  • 8.3 Cardiovascular Disorders
    • 8.3.1 Market Trends
    • 8.3.2 Market Forecast
  • 8.4 Hematological Disorders
    • 8.4.1 Market Trends
    • 8.4.2 Market Forecast
  • 8.5 Others
    • 8.5.1 Market Trends
    • 8.5.2 Market Forecast

9 Market Breakup by Manufacturing

  • 9.1 Outsourced
    • 9.1.1 Market Trends
    • 9.1.2 Market Forecast
  • 9.2 In-House
    • 9.2.1 Market Trends
    • 9.2.2 Market Forecast

10 Market Breakup by Region

  • 10.1 North America
    • 10.1.1 United States
      • 10.1.1.1 Market Trends
      • 10.1.1.2 Market Forecast
    • 10.1.2 Canada
      • 10.1.2.1 Market Trends
      • 10.1.2.2 Market Forecast
  • 10.2 Asia-Pacific
    • 10.2.1 China
      • 10.2.1.1 Market Trends
      • 10.2.1.2 Market Forecast
    • 10.2.2 Japan
      • 10.2.2.1 Market Trends
      • 10.2.2.2 Market Forecast
    • 10.2.3 India
      • 10.2.3.1 Market Trends
      • 10.2.3.2 Market Forecast
    • 10.2.4 South Korea
      • 10.2.4.1 Market Trends
      • 10.2.4.2 Market Forecast
    • 10.2.5 Australia
      • 10.2.5.1 Market Trends
      • 10.2.5.2 Market Forecast
    • 10.2.6 Indonesia
      • 10.2.6.1 Market Trends
      • 10.2.6.2 Market Forecast
    • 10.2.7 Others
      • 10.2.7.1 Market Trends
      • 10.2.7.2 Market Forecast
  • 10.3 Europe
    • 10.3.1 Germany
      • 10.3.1.1 Market Trends
      • 10.3.1.2 Market Forecast
    • 10.3.2 France
      • 10.3.2.1 Market Trends
      • 10.3.2.2 Market Forecast
    • 10.3.3 United Kingdom
      • 10.3.3.1 Market Trends
      • 10.3.3.2 Market Forecast
    • 10.3.4 Italy
      • 10.3.4.1 Market Trends
      • 10.3.4.2 Market Forecast
    • 10.3.5 Spain
      • 10.3.5.1 Market Trends
      • 10.3.5.2 Market Forecast
    • 10.3.6 Russia
      • 10.3.6.1 Market Trends
      • 10.3.6.2 Market Forecast
    • 10.3.7 Others
      • 10.3.7.1 Market Trends
      • 10.3.7.2 Market Forecast
  • 10.4 Latin America
    • 10.4.1 Brazil
      • 10.4.1.1 Market Trends
      • 10.4.1.2 Market Forecast
    • 10.4.2 Mexico
      • 10.4.2.1 Market Trends
      • 10.4.2.2 Market Forecast
    • 10.4.3 Others
      • 10.4.3.1 Market Trends
      • 10.4.3.2 Market Forecast
  • 10.5 Middle East and Africa
    • 10.5.1 Market Trends
    • 10.5.2 Market Breakup by Country
    • 10.5.3 Market Forecast

11 SWOT Analysis

  • 11.1 Overview
  • 11.2 Strengths
  • 11.3 Weaknesses
  • 11.4 Opportunities
  • 11.5 Threats

12 Value Chain Analysis

13 Porters Five Forces Analysis

  • 13.1 Overview
  • 13.2 Bargaining Power of Buyers
  • 13.3 Bargaining Power of Suppliers
  • 13.4 Degree of Competition
  • 13.5 Threat of New Entrants
  • 13.6 Threat of Substitutes

14 Price Analysis

15 Competitive Landscape

  • 15.1 Market Structure
  • 15.2 Key Players
  • 15.3 Profiles of Key Players
    • 15.3.1 AbbVie Inc.
      • 15.3.1.1 Company Overview
      • 15.3.1.2 Product Portfolio
      • 15.3.1.3 Financials
      • 15.3.1.4 SWOT Analysis
    • 15.3.2 Amgen Inc.
      • 15.3.2.1 Company Overview
      • 15.3.2.2 Product Portfolio
      • 15.3.2.3 Financials
      • 15.3.2.4 SWOT Analysis
    • 15.3.3 AstraZeneca plc
      • 15.3.3.1 Company Overview
      • 15.3.3.2 Product Portfolio
      • 15.3.3.3 Financials
      • 15.3.3.4 SWOT Analysis
    • 15.3.4 F. Hoffmann-La Roche Ltd
      • 15.3.4.1 Company Overview
      • 15.3.4.2 Product Portfolio
      • 15.3.4.3 SWOT Analysis
    • 15.3.5 GlaxoSmithKline plc
      • 15.3.5.1 Company Overview
      • 15.3.5.2 Product Portfolio
      • 15.3.5.3 Financials
      • 15.3.5.4 SWOT Analysis
    • 15.3.6 Johnson & Johnson
      • 15.3.6.1 Company Overview
      • 15.3.6.2 Product Portfolio
      • 15.3.6.3 Financials
      • 15.3.6.4 SWOT Analysis
    • 15.3.7 Merck KGaA
      • 15.3.7.1 Company Overview
      • 15.3.7.2 Product Portfolio
      • 15.3.7.3 Financials
      • 15.3.7.4 SWOT Analysis
    • 15.3.8 Novartis AG
      • 15.3.8.1 Company Overview
      • 15.3.8.2 Product Portfolio
      • 15.3.8.3 Financials
      • 15.3.8.4 SWOT Analysis
    • 15.3.9 Pfizer Inc.
      • 15.3.9.1 Company Overview
      • 15.3.9.2 Product Portfolio
      • 15.3.9.3 Financials
      • 15.3.9.4 SWOT Analysis
    • 15.3.10 Sanofi
      • 15.3.10.1 Company Overview
      • 15.3.10.2 Product Portfolio
      • 15.3.10.3 Financials
      • 15.3.10.4 SWOT Analysis
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