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U.S. Non-oncology Biopharmaceuticals Market Analysis & Forecast: 2026-2033

U.S. Non-oncology Biopharmaceuticals Market, By Product Type (Biologics and Biosimilars), By Drug Class (Monoclonal Antibody, Enzyme Replacement Therapy, Erythropoietin, Interferon, Colony-stimulating Factor, Botulinum Toxin, Fusion Protein, Vaccines, Human Recombinant Insulin, Blood Factors, Human Growth Hormone, and Others), By Disease Indication (Diabetes, Rheumatoid Arthritis, Psoriatic Arthritis, Multiple Sclerosis, Hemophilia, Anemia, Age-related Macular Degeneration, Hepatitis B, Cystic Fibrosis, Osteoporosis, Crohn’s Disease, Ulcerative Colitis, Psoriasis, Ankylosing Spondylitis, and Others (Cardiac Diseases and Others))

  • Published In : 23 Jan, 2026
  • Code : CMI2575
  • Page number :153
  • Formats :
      Excel and PDF :
  • Industry : Pharmaceutical
  • Historical Range : 2020 - 2024
  • Forecast Period : 2026 - 2033

U.S. Non-oncology Biopharmaceuticals Market Size and Trends: 2026-2033

U.S. non-oncology biopharmaceuticals market is estimated to be valued at USD 252 Bn in 2026 and is expected to reach USD 497 Bn by 2033, exhibiting a compound annual growth rate (CAGR) of 10.2% from 2026 to 2033.

Key Takeaways

  • Based on Product Type, the Biologics segment is expected to lead the market with 85% share in 2026, due to their widespread use across chronic and complex disease treatments.
  • Based on Drug Class, the Monoclonal Antibody segment is expected to hold 40% share of the market in 2026, owing to their extensive application in autoimmune, inflammatory, and metabolic disorders.
  • By Disease Indication, Diabetes is projected to account for 18% share of the market in 2026, driven by strong demand for human recombinant insulin and other biologic therapies.

Market Overview

Rising incidence of chronic diseases like diabetes, autoimmune diseases, and rare genetic disorders is fueling the demand for biopharmaceuticals that are not used in oncology in the U.S. The rising trend of using biologics like monoclonal antibodies, recombinant proteins, and insulin-based therapies is propelling the growth of the biopharmaceutical market. Constant developments in biotechnology and R&D investment have resulted in the entry of innovative drugs that have better efficacy and safety. 

Current Events and Its Impacts on the U.S. Non-oncology Biopharmaceuticals Market

Current Events

and its impact

FDA Regulatory Reform and Policy Changes

  • Description: Accelerated Approval Pathway Reviews
  • Impact: Potential for faster market entry of non-oncology drugs, reducing time-to-market and increasing revenue opportunities
  • Description: Real-World Evidence Integration Requirements
  • Impact: Higher compliance costs but improved post-market surveillance may enhance drug safety profiles and market confidence

Medicare Drug Price Negotiation Implementation

  • Description: IRA Drug Price Negotiation Expansion
  • Impact: Direct government pricing pressure on high-cost non-oncology biologics and specialty drugs, potentially reducing revenues
  • Description: Medicare Part D Coverage Gap Reforms
  • Impact: Improved patient access to non-oncology medications may increase volume but at lower reimbursement rates

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How is Product Innovation driving the growth in the U.S. non-oncology biopharmaceuticals market?

  • Next-Generation Biologics: Improvements in the manufacture of more potent monoclonal antibodies, fusion proteins, and enzyme therapies with greater safety profiles and longer dosing cycles.
  • Targeted Therapies: Precision medicine targeted at specific patients with a certain genetic profile or disease fingerprint.
  • Advanced Drug Delivery Systems: These include sustained release systems, prefilled pens, and automatic injectors meant to enhance patient compliance.
  • Combination Therapies: Utilization of biopharmaceuticals as a combination with traditional pharmaceuticals or biologics to provide improved efficacy against chronic diseases.
  • Wireless Health Integration: Devices that allow for tracking of patient response to treatment and treatment compliance.

Segmental Insights

U.S. Non-oncology Biopharmaceuticals Market By Product Type

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U.S. Non-Oncology Biopharmaceuticals Market Insights, By Product Type – Biologics dominate due to widespread use in chronic and complex diseases

Based on product type, the Biologics segment is projected to hold the highest market share of 85% in 2026, due to its widespread demand and application within the treatment of chronic and complex diseases. Biologics, such as monoclonal antibodies, recombinant proteins, and hormone products, form a favored class within the treatment of those diseases, in particular those with a high need for targeted and more effective and safe drugs.
For instance, in July 2025, Biocon Biologics received U.S. FDA approval for their product, “Kirsty™”, which is the “first and only interchangeable rapid-acting insulin aspart biosimilar,” a biologic, for treatment of diabetes in the United States.

U.S. Non-Oncology Biopharmaceuticals Market Insights, By Drug Class – Monoclonal Antibodies lead due to targeted applications in autoimmune and metabolic disorders

In terms of drug class, the Monoclonal Antibody segment is estimated to contribute the highest market share of 40% in 2026, owing to their widespread application in autoimmune, inflammatory, and metabolic disorders. Monoclonal antibodies are highly specific therapies that target disease-causing proteins, offering improved efficacy and reduced side effects compared to traditional treatments.
For instance, in April 2025, Johnson & Johnson achieved FDA approval for its new treatment IMAAVY™ (nipocalimab-aahu), a new monoclonal antibody that blocks the mechanism of FcRn to treat generalized myasthenia gravis (gMG) for individuals 12 years of age and older.

U.S. Non-Oncology Biopharmaceuticals Market Insights, By Disease Indication – Diabetes leads due to strong demand for human recombinant insulin and other biologics

Based on disease indication, Diabetes is expected to hold a market share of 18% in 2026, led by high demand for human recombinant insulin, GLP-1 analogues, and other biological products. The incidence rate of diabetes, awareness among patients, and advancements in devices to deliver insulin are some factors contributing to this growth.

For instance, in February 2025, the U.S. FDA approved Merilog (insulin-aspart-szjj), a new biosimilar insulin with a quick-acting indication (to Novolog), for the improvement of glycemic control in adults as well as pediatric patients with diabetes

Market Report Scope

U.S. Non-oncology Biopharmaceuticals Market Report Coverage

Report Coverage Details
Base Year: 2025 Market Size in 2026: USD 252 Bn
Historical Data for: 2020 To 2024 Forecast Period: 2026 To 2033
Forecast Period 2026 to 2033 CAGR: 10.2% 2033 Value Projection: USD 497 Bn
Segments covered:
  • By Product Type: Biologics and Biosimilars
  • By Drug Class: Monoclonal Antibody, Enzyme Replacement Therapy, Erythropoietin, Interferon, Colony-stimulating Factor, Botulinum Toxin, Fusion Protein, Vaccines, Human Recombinant Insulin, Blood Factors, Human Growth Hormone, and Others.
  • By Disease Indication: Diabetes, Rheumatoid Arthritis, Psoriatic Arthritis, Multiple Sclerosis, Hemophilia, Anemia, Age-related Macular Degeneration, Hepatitis B, Cystic Fibrosis, Osteoporosis, Crohn’s Disease, Ulcerative Colitis, Psoriasis, Ankylosing Spondylitis, and other conditions including cardiac diseases and others.
Companies covered:

Sanofi S.A., Pfizer, Inc., Johnson & Johnson, Novartis International AG, Amgen, Inc., Eli Lilly and Company, AbbVie Inc., Bristol-Myers Squibb Company, F. Hoffmann-La Roche AG, Novo Nordisk A/S, GlaxoSmithKline plc., UCB Pharma, Teva Pharmaceutical Industries Ltd., Takeda Pharmaceutical Company Ltd, AstraZeneca Plc, Mylan N.V., LEO Pharma A/S, Boehringer Ingelheim GmbH, Alexion Pharmaceuticals Inc., Merck & Co., Inc., Elusys Therapeutics, Inc., Swedish Orphan Biovitrum AB, Samsung Bioepis NL B.V., Biogen Inc., and Theratechnologies Inc.

Growth Drivers:
  • Rising prevalence of chronic and rare diseases
  • Increasing adoption of biologics and targeted therapies
Restraints & Challenges:
  • Development of next-generation biologics and biosimilars
  • Expansion of digital health and remote patient monitoring

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U.S. Non-Oncology Biopharmaceuticals Market Driver

Rising prevalence of chronic and rare diseases

Rise in prevalence of chronic diseases like diabetes, autoimmune diseases, and rare genetic disorders in the U.S. drives the demand for non-oncology biopharmaceuticals. Patients and healthcare professionals are also demanding innovative biologic medications such as monoclonal antibodies, enzyme replacements, and recombinant proteins due to their greater potency and safety compared to conventional medications. Increasing awareness and treatment rates of such diseases also fuel the demand.

U.S. Non-Oncology Biopharmaceuticals Market Opportunity

Innovation in biologics and biosimilars

The market offers considerable growth opportunities in the next-generation biologics and biosimilars area. The launch of new therapies with optimized dosing regimens, advanced delivery platforms, or mechanism of action can help in improving patient compliance and extending the therapeutic armamentarium. Furthermore, extending the biosimilar offering can help in making the therapies more affordable, which can also be a competitive edge opportunity in the market.

Analyst Opinion (Expert Opinion)

  • The U.S. non-oncology biopharmaceuticals market is undergoing a strategic shift in becoming a highly innovative segment. The monoclonal antibodies have largely become mainstream therapies in autoimmune, metabolic, and inflammatory diseases, not only due to their relevance in the respective conditions, but also owing to the pricing power they have been able to demonstrate.
  • Pipeline activity and launch of products reflect that the market is shifting towards the era of precision and convenience-based treatments. Next-generation biologics are also being developed with better treatment regimen options, patient-friendly delivery methods, and combination strategies, which improve patient compliance and extend the patient base.
  • Strategically, investments are happening in the arena of portfolio diversification management. Biologics continue to represent high-revenue therapeutic areas, but intelligent growth into biosimilars, niche rare diseases, and holistic digital health is a key differentiator. Today, the pharmaceutical market is no longer defined by the development of a molecule alone, but more and more by patient-oriented distribution and affordability and evidence-based outcomes.

U.S. Non-oncology Biopharmaceuticals Industry News

  • In December 2025, Emcutix Biopharmaceuticals Limited—a dermatology-focused, wholly owned subsidiary of Emcure Pharmaceuticals Ltd. unveiled SOLGLO-AZ Liposomal Serum, featuring a unique formulation powered by Lipotwin Technology and the Hyperboost Brightening Complex.

Market Segmentation

  • Product Type Insights (Revenue, USD Bn, 2026 - 2033)
    • Biologics
    • Biosimilars
  • Drug Class Insights (Revenue, USD Bn, 2026 - 2033)
    • Monoclonal Antibody
    • Enzyme Replacement Therapy
    • Erythropoietin
    • Interferon
    • Colony-stimulating Factor
    • Botulinum Toxin
    • Fusion Protein
    • Vaccines
    • Human Recombinant Insulin
    • Blood Factors
    • Human Growth Hormone
    • Others
  • Disease Indication Insights (Revenue, USD Bn, 2026 - 2033)
    • Diabetes
    • Rheumatoid Arthritis
    • Psoriatic Arthritis
    • Multiple Sclerosis
    • Hemophilia
    • Anemia
    • Age-related Macular Degeneration
    • Hepatitis B
    • Cystic Fibrosis
    • Osteoporosis
    • Crohn’s Disease
    • Ulcerative Colitis
    • Psoriasis
    • Ankylosing Spondylitis
    • Others (Cardiac diseases and others)
  • Key Players Insights
    • Sanofi S.A., Pfizer, Inc.
    • Johnson & Johnson
    • Novartis International AG
    • Amgen, Inc.
    • Eli Lilly and Company
    • AbbVie Inc.
    • Bristol-Myers Squibb Company
    • Hoffmann-La Roche AG,
    • Novo Nordisk A/S
    • GlaxoSmithKline plc.
    • UCB Pharma
    • Teva Pharmaceutical Industries Ltd.
    • Takeda Pharmaceutical Company Ltd
    • AstraZeneca Plc
    • Mylan N.V.
    • LEO Pharma A/S
    • Boehringer Ingelheim GmbH
    • Alexion Pharmaceuticals Inc.
    • Merck & Co., Inc.
    • Elusys Therapeutics, Inc.
    • Swedish Orphan Biovitrum AB
    • Samsung Bioepis NL B.V., Biogen Inc.
    • Theratechnologies Inc

Sources

Primary Research interviews

  • Interviews with key executives, medical affairs specialists, and R&D leaders from leading U.S. biopharmaceutical companies such as AbbVie, Amgen, Pfizer, Johnson & Johnson, and Novartis.
  • Discussions with oncologists, endocrinologists, and autoimmune disease specialists to understand treatment patterns, adoption of biologics, and patient preferences.

Databases

  • U.S. FDA Drug Approvals Database (Drugs@FDA)
  • ClinicalTrials.gov – registry of ongoing and completed clinical trials
  • National Library of Medicine (PubMed) databases for clinical and pharmacological data
  • U.S. Centers for Medicare & Medicaid Services (CMS) data for drug utilization and reimbursement trends

Magazines

  • Pharmaceutical Executive
  • BioPharm International
  • Genetic Engineering & Biotechnology News (GEN)

Journals

  • New England Journal of Medicine (NEJM)
  • The Lancet
  • Journal of Clinical Oncology (JCO)
  • Nature Biotechnology

Newspapers

  • The Wall Street Journal – Health & Pharmaceuticals Section
  • The New York Times – Health & Science Section
  • Reuters Health & Pharma News
  • Financial Times – Healthcare & Biopharma News

Associations

  • Pharmaceutical Research and Manufacturers of America (PhRMA)
  • Biotechnology Innovation Organization (BIO)
  • American Diabetes Association (ADA)
  • American Autoimmune Related Diseases Association (AARDA)

Public Domain sources

  • U.S. National Institutes of Health (NIH) publications and reports
  • U.S. Food and Drug Administration (FDA) press releases
  • Centers for Disease Control and Prevention (CDC) disease statistics
  • U.S. Department of Health & Human Services (HHS) policy reports

Proprietary Elements

  • CMI Data Analytics Tool
  • Proprietary CMI Existing Repository of information for last 8 years

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About Author

Vipul Patil is a dynamic management consultant with 6 years of dedicated experience in the pharmaceutical industry. Known for his analytical acumen and strategic insight, Vipul has successfully partnered with pharmaceutical companies to enhance operational efficiency, cross broader expansion, and navigate the complexities of distribution in markets with high revenue potential.

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Frequently Asked Questions

The U.S. Non-Oncology Biopharmaceuticals Market is estimated to be valued at USD 252 Bn in 2026, and is expected to reach USD 497 Bn by 2033.

The CAGR of the U.S. Non-Oncology Biopharmaceuticals Market is projected to be 10.2% from 2026 to 2033.

Rising prevalence of chronic diseases, growing adoption of biologics and targeted therapies, product innovation in delivery systems, and expansion of biosimilars are major factors driving market growth

High therapy costs, complex regulatory approvals, and limited patient access in certain rare disease segments are major factors hampering market growth.

The biologics segment is expected to lead the market, driven by widespread application in chronic and complex diseases.

Sanofi S.A., Pfizer, Inc., Johnson & Johnson, Novartis International AG, Amgen, Inc., Eli Lilly and Company, AbbVie Inc., Bristol-Myers Squibb Company, F. Hoffmann-La Roche AG, Novo Nordisk A/S, GlaxoSmithKline plc., UCB Pharma, Teva Pharmaceutical Industries Ltd., Takeda Pharmaceutical Company Ltd, AstraZeneca Plc, Mylan N.V., LEO Pharma A/S, Boehringer Ingelheim GmbH, Alexion Pharmaceuticals Inc., Merck & Co., Inc., Elusys Therapeutics, Inc., Swedish Orphan Biovitrum AB, Samsung Bioepis NL B.V., Biogen Inc., and Theratechnologies Inc.

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