Ultra Market Research | Stem Cell Therapy for Respiratory Disorders Market

Stem Cell Therapy for Respiratory Disorders Market

  • Report ID : 1211

  • Category : Therapeutic-Area

  • No Of Pages : 230

  • Published on: October 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 Monoclonal Antibodies Market: Trends, Growth, and Strategic Insights
Introduction
Crohn’s disease, a chronic inflammatory bowel condition, has seen a significant rise in prevalence globally, prompting advancements in therapeutic interventions. Monoclonal antibodies (mAbs) have emerged as pivotal treatments, offering targeted approaches to manage and potentially induce remission in patients. This article delves into the current landscape of the Crohn’s disease monoclonal antibodies market, examining its growth trajectory, key players, and future prospects.

 

Market Overview
Global Relevance and Economic Impact
Global Crohn’s disease market was valued at approximately USD 10.8 billion in 2024, with monoclonal antibodies accounting for a significant portion due to their efficacy in treatment 
The economic burden of Crohn’s disease is substantial, encompassing direct medical costs and indirect costs such as lost productivity. The introduction of mAbs has not only improved patient outcomes but also influenced healthcare expenditures and insurance models worldwide.

 

Key Statistics and Recent Developments

Monoclonal antibodies market is projected to grow at a compound annual growth rate (CAGR) of 4.3% from 2024 to 2034 

Approximately 8–10% of the Crohn’s disease market comprises pediatric patients 

The United States represents about 78% of the market share in the seven major markets (7MM) 

 

Market Segmentation
By Product Type
Monoclonal antibodies in Crohn’s disease treatment primarily include:

TNF Inhibitors: Such as infliximab (Remicade) and adalimumab (Humira), which have been cornerstone therapies.

Integrin Inhibitors: Like vedolizumab (Entyvio), targeting gut-specific adhesion molecules.

IL-12/IL-23 Inhibitors: Including ustekinumab (Stelara), which modulate immune responses.

Emerging Therapies: Such as mirikizumab (Eli Lilly) and duvakitug (Teva/Sanofi), currently in advanced clinical stages 
Investors
 

By Application/End-Use Industry
Hospitals and Clinics: Primary settings for mAb administration, especially intravenous formulations.

Home Healthcare: Increasing adoption of subcutaneous mAb therapies for at-home administration.

Pharmaceutical and Biotech Companies: Involved in the development and commercialization of mAb therapies.

 

By Region
North America: Dominates the market, driven by high disease prevalence and advanced healthcare infrastructure.

Europe: Significant market share with increasing adoption of biologic therapies.

Asia-Pacific: Emerging market with rising awareness and healthcare improvements.

Latin America and MEA: Smaller markets with potential for growth due to improving healthcare access.

 

Key Market Players
Top Companies
AbbVie: Market leader with Humira and Rinvoq, focusing on immunology.

Eli Lilly: Advancing with mirikizumab and strategic acquisitions like Morphic Holding 
Reuters

Teva Pharmaceuticals: Partnering with Sanofi on duvakitug, showing promising Phase 2 results 
Investors

Johnson & Johnson: Offers Stelara and is exploring new mAb therapies.

Pfizer: Expanding its portfolio through acquisitions and partnerships.

Strategic Developments
Mergers and Acquisitions: Eli Lilly's acquisition of Morphic Holding for $3.2 billion enhances its IBD portfolio 
Reuters

New Launches: Introduction of subcutaneous formulations and oral mAbs to improve patient compliance.

Partnerships: Collaborations between pharmaceutical companies to co-develop and commercialize new therapies.

 

Market Drivers
Increasing Disease Prevalence: Rising incidence of Crohn’s disease globally.

Advancements in Biologic Therapies: Development of more targeted and effective treatments.

Improved Diagnostic Techniques: Early detection leading to better management.

Rising Healthcare Expenditure: Enabling access to advanced therapies.

 

Market Restraints
High Treatment Costs: Expensive mAb therapies limiting accessibility.

Regulatory Challenges: Lengthy approval processes for new treatments.

Adverse Effects: Potential side effects leading to treatment discontinuation.

Market Competition: Presence of biosimilars affecting market share.

 

Opportunities & Future Trends
Pediatric Market Expansion: Development of mAbs tailored for younger populations.

Oral and Subcutaneous Formulations: Enhancing patient convenience and adherence.

Emerging Markets: Growth in regions with improving healthcare infrastructure.

Personalized Medicine: Tailoring treatments based on genetic profiles.

 

Regional Insights
North America: Continues to lead with robust healthcare systems and high adoption rates of biologics.

Europe: Strong market presence with increasing patient access to advanced therapies.

Asia-Pacific: Rapidly growing market due to urbanization and healthcare improvements.

Latin America and MEA: Expanding markets with rising healthcare investments and disease awareness.

A1: The market includes all commercial and clinical activities around using stem cells (mesenchymal stem cells, induced pluripotent stem cells, etc.), their derivatives (exosomes, conditioned media), delivery platforms, and related services to prevent, treat, or manage respiratory disorders such as COPD, ARDS, pulmonary fibrosis, asthma, and COVID-19–related lung injury.
Major product types include autologous and allogeneic cell therapies (MSC, iPSC-derived cells), cell-derived products (exosomes, secretomes), delivery systems (nebulizers, intratracheal/IV devices), and supporting technologies (cell processing, cryopreservation, GMP manufacturing, companion diagnostics).
North America (especially the U.S.) leads in clinical trials, funding, and manufacturing capacity, followed by Europe (UK, Germany, Netherlands) and parts of Asia Pacific (China, South Korea, Japan) where both clinical development and manufacturing scale are growing.
The pandemic accelerated interest and clinical testing of cell therapies for ARDS and COVID-related lung injury, bringing funding and trial activity. It also highlighted the need for scalable manufacturing and rapid regulatory pathways, but long-term commercial impact depends on definitive efficacy data.
Opportunities include developing scalable manufacturing solutions, cell-free therapeutics (exosomes), novel pulmonary delivery devices, biomarker-driven precision therapies, and services (CDMO/CRO) that solve bottlenecks in production and regulatory compliance.

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