Ultra Market Research | Crohn’s Disease Immunotherapy Market
SEO Alt Text: Global Crohn’s Disease Immunotherapy Market Overview – Trends, Growth Drivers & Innovations in Biologic Treatments

Crohn’s Disease Immunotherapy Market

  • Report ID : 1185

  • Category : Therapeutic-Area

  • No Of Pages : 240

  • Published on: July 2025

  • Status: Published

  • Format : Power Point PDF Excel Word

Key Question Answer

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Global Market Outlook

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In-depth analysis of global and regional trends

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Analyze and identify the major players in the market, their market share, key developments, etc.

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To understand the capability of the major players based on products offered, financials, and strategies.

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Identify disrupting products, companies, and trends.

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To identify opportunities in the market.

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Analyze the regional penetration of players, products, and services in the market.

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Comparison of major players financial performance.

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Evaluate strategies adopted by major players.

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Recommendations

Crohn’s Disease Immunotherapy Market: Global Trends, Growth Drivers, and Forecast Analysis (2025–2032)
Introduction

Crohn’s Disease Immunotherapy Market is gaining momentum globally due to the increasing prevalence of inflammatory bowel diseases (IBDs), advancements in biologics, and the growing demand for personalized medicine. Crohn’s disease is a chronic autoimmune disorder that affects the gastrointestinal tract, leading to inflammation, pain, and severe complications. As conventional treatments often fall short of providing long-term relief, immunotherapy is emerging as a promising solution. This article provides a comprehensive, data-driven analysis of the Crohn’s Disease Immunotherapy market, exploring its current landscape, key trends, growth drivers, challenges, and future outlook.


Market Overview
Global Crohn’s Disease Immunotherapy market has witnessed significant expansion in recent years. With rising awareness of IBDs and the availability of advanced treatment options, immunotherapy is becoming a mainstream approach in disease management. Immunotherapy works by modulating the immune system to reduce inflammation and disease progression, thereby improving patients' quality of life.
According to recent reports, the market size was valued at USD 4.6 billion in 2023 and is projected to reach USD 8.1 billion by 2032, growing at a CAGR of 6.5% from 2024 to 2032. The market growth is largely attributed to increasing R&D investments, favorable regulatory environments, and a surge in the incidence rate of Crohn’s disease globally.


Global Relevance and Economic Impact
Crohn’s disease affects approximately 3 million people in the United States and millions more worldwide. The disease imposes a substantial burden on healthcare systems, with high treatment costs and hospitalizations. Immunotherapy, particularly biologics, has demonstrated efficacy in reducing flare-ups and promoting mucosal healing, thereby lowering the long-term healthcare costs.
The economic impact of Crohn’s disease is multifaceted, involving direct medical expenses, loss of productivity, and long-term disability. The shift toward biologics and biosimilars in immunotherapy not only enhances patient outcomes but also contributes to cost optimization, creating a ripple effect in the healthcare economy.


Key Statistics and Recent Developments

  • Market Size (2023): USD 4.6 Billion
  • Forecast (2032): USD 8.1 Billion
  • CAGR (2024–2032): 6.5%
  • Biologics Dominance: Biologics account for over 65% of market revenue
  • Top Growth Region: North America (holding over 40% of the global market share)
  • Recent Approvals: Ustekinumab (Stelara), Risankizumab (Skyrizi), and biosimilars like Adalimumab biosimilar (Amgevita)

  • Market Segmentation
    By Product Type
  • Monoclonal Antibodies (mAbs)
  • Cytokine Inhibitors
  • Checkpoint Inhibitors
  • Interleukin Inhibitors
  • Biosimilars
  • Other Biologics


By Application/End-Use Industry

  • Hospitals
  • Specialty Clinics
  • Homecare Settings
  • Academic & Research Institutes


By Region

  • U.S


Key Market Players

  • AbbVie Inc. – Market leader with its blockbuster drug Humira (adalimumab).
  • Johnson & Johnson (Janssen Biotech) – Manufacturer of Stelara (ustekinumab), widely used in Crohn’s treatment.
  • Pfizer Inc. – Offers Xeljanz (tofacitinib) and exploring JAK inhibitors for IBD.
  • Takeda Pharmaceuticals – Developed Entyvio (vedolizumab), a gut-selective integrin blocker.
  • Amgen Inc. – Leading biosimilar provider with Amgevita, a biosimilar to Humira.
  • Eli Lilly and Company – Actively engaged in R&D for immunomodulatory therapies.
  • Biogen Inc. – Expanding portfolio in neuro-immune disorders and inflammation.
  • Bristol Myers Squibb – Focused on checkpoint inhibitors for autoimmune diseases.
  • Samsung Bioepis – A major player in biosimilars, partnered with Biogen.
  • Celltrion Healthcare – Known for developing infliximab biosimilars like Remsima.


Strategic Developments

  • Mergers & Acquisitions: Amgen acquired rights to global biosimilars portfolio from Pfizer.
  • New Launches: FDA approval of Skyrizi (risankizumab) for Crohn’s in 2022.
  • Collaborations: Janssen partnered with Morphic Therapeutic for novel integrin therapeutics.


Market Drivers

  • Rising Prevalence of IBDs: Increasing global incidence of Crohn’s disease and ulcerative colitis.
  • Advanced Biologic Therapies: mAbs and interleukin inhibitors offer targeted, effective treatments.
  • Favorable Reimbursement Policies: Supportive coverage for biologics in developed markets.
  • Pipeline Expansion: Over 80 active clinical trials related to Crohn’s disease immunotherapy.
  • Growing Awareness and Diagnosis Rates: Enhanced diagnostics promoting early intervention.


Market Restraints

  • High Cost of Biologics: Average treatment can cost $20,000–$50,000 annually.
  • Biosimilar Competition: Pressure on pricing and market exclusivity.
  • Regulatory Barriers: Complex approval processes for novel biologics.
  • Adverse Effects: Risk of infections and malignancy with long-term immunosuppression.
  • Limited Access in Low-Income Regions: Infrastructure and affordability constraints.


Opportunities and Future Trends

  • Emerging Markets Expansion: Untapped opportunities in Asia-Pacific and Latin America.
  • Development of Oral Biologics: Enhanced patient compliance and convenience.
  • Precision Medicine: Integration of genetic profiling to customize therapy.
  • AI in Drug Development: Faster identification of novel immunologic targets.
  • Rise in Biosimilar Adoption: Cost-effective alternatives boosting market penetration.


Regional Insights
North America
Dominates the global Crohn’s Disease immunotherapy market.
Strong R&D infrastructure and government support.
Key players headquartered in the U.S.
Europe
Second-largest market.
Increasing adoption of biosimilars in countries like Germany and the UK.
Asia-Pacific
Fastest-growing region.
Growth fueled by rising awareness, improved healthcare infrastructure, and government initiatives.
Latin America
Gradual adoption of biologics.
Public-private partnerships to improve accessibility.
Middle East & Africa
Market in early development stages.
Focused efforts on healthcare expansion and access to specialty drugs.
 

Strategic Recommendations for Stakeholders

  • Investors: Explore opportunities in biosimilars and emerging markets.
  • Pharma Companies: Focus on R&D and collaborative partnerships for novel immunotherapies.
  • Healthcare Providers: Adopt evidence-based treatment guidelines and expand access to biologics.
  • Policy Makers: Facilitate approval pathways and improve pricing models for advanced therapies.


Target Audience

  • This report is particularly relevant to:
  • Investors exploring healthcare sector opportunities
  • Pharmaceutical and biotech firms developing IBD therapies
  • Regulatory bodies and policymakers
  • Healthcare providers and hospital systems
  • Academic researchers in immunology and gastroenterology
As of 2024, the global Crohn’s Disease Immunotherapy Market is estimated to be valued at USD 8.2 billion, and it is projected to reach around USD 13.6 billion by 2030, growing at a CAGR of 7.5% during the forecast period (2024–2030).
FDA and EMA are pushing for fast-track and orphan drug designations to speed up drug development. Biosimilar guidelines are evolving to promote competition. Regulatory harmonization is improving access in emerging economies.
Biosimilars are increasingly entering the market post-patent expiration of key biologics. They offer cost-effective treatment options, particularly in Europe and Asia-Pacific, and are expected to expand accessibility.
Hospitals Specialty Clinics Ambulatory Surgical Centers Research Institutes

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