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Dupixent Market Summary
The global dupixent market size was estimated at USD 14.15 billion in 2024, and is projected to reach USD 27.58 billion by 2033, growing at a CAGR of 7.70% from 2025 to 2033. The Dupixent industry reflects a transition from traditional therapies to biologics.
Anchored by its innovative interleukin-4 and interleukin-13 inhibition mechanism, this growth is driven by the increasing global prevalence of Type 2 inflammatory diseases, including atopic dermatitis, asthma, and chronic rhinosinusitis with nasal polyps, along with recent regulatory approvals for new indications such as bullous pemphigoid and eosinophilic esophagitis. The market growth is driven by the need for treatments addressing Type 2 inflammatory diseases. Dupixent, developed by Sanofi and Regeneron, demonstrates efficacy and safety in clinical trials, surpassing conventional options like corticosteroids for conditions including atopic dermatitis and asthma. This shift is supported by increasing global prevalence, with over 200 million atopic dermatitis patients and 300 million asthma cases reported in 2024.
Research and development efforts are a key driver of the Dupixent market's expansion, supported by clinical trials across new therapeutic areas. Ongoing studies such as LIBERTY-CSU CUPID for chronic spontaneous urticaria and trials in allergic fungal rhinosinusitis aim to broaden the drug's reach to new patient populations. Pediatric trials for eosinophilic esophagitis and approved use in bullous pemphigoid (January 2024) are expected to enhance patient eligibility and strengthen long-term revenue generation through 2033. These initiatives, supported by real-world evidence, are increasing Dupixent's positioning across inflammatory and rare immunologic indications.
Sanofi and Regeneron's global collaboration facilitates accelerated regulatory approvals and strengthens market access infrastructure. U.S. FDA approvals in June 2025 for COPD and bullous pemphigoid mark strategic milestones, expanding Dupixent's approved indications to nine, including chronic rhinosinusitis with nasal polyps and prurigo nodularis. This has reinforced the drug's standing in the interleukin inhibitor class, with global rollout in North America, Europe, and Asia Pacific driven by a coordinated regulatory and commercialization strategy.
Patent protection in major markets such as the U.S. and Japan until 2033 reduces biosimilar competition risk in the medium term. Additionally, manufacturing complexity and specialized facilities act as deterrents for new entrants. Market expansion opportunities remain in underpenetrated regions, particularly Latin America and the Middle East & Africa. Countries such as Brazil and Saudi Arabia present significant patient pools, supported by healthcare reforms and increasing biologics demand. Localized pricing strategies and distribution partnerships are expected to drive regional access.
Regulatory incentives such as orphan drug exclusivity in Europe, combined with a strong development pipeline, support sustained growth. However, post-2033 market dynamics, including biosimilar entry and pricing constraints in Europe and Asia Pacific, highlight the need for adaptive reimbursement strategies and patient access programs to maintain profitability.
Global Dupixent Market Report Segmentation
This report forecasts revenue growth at the global, regional, and country levels and provides an analysis of the latest industry trends in each of the sub-segments from 2021 to 2033. For this study, Grand View Research has segmented the global Dupixent market report based on indication, distribution channel, and region: