PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2063563
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2063563
According to Mordor Intelligence, the tree nut allergy market size is projected to expand from USD 299.85 million in 2025 and USD 320.40 million in 2026 to USD 446.98 million by 2031, registering a CAGR of 6.88% between 2026 to 2031.

This report is Segmented by Product Type (Acute Care Drugs, Disease-Modifying Therapies, Diagnostics), Tree Nut Type (Walnut, Cashew, Almond, Hazelnut, and More), End User (Hospital Pharmacies, Retail Pharmacies, and More), Age Group (Paediatric, Adult, Geriatric), and Geography (North America, Europe, Asia-Pacific, Middle East and Africa, South America). Market Forecasts are Provided in Terms of Value (USD).
A 2024 Turkish cohort reported that 60% of newly diagnosed tree-nut allergic children experienced multi-system reactions requiring epinephrine. Additionally, a 2025 European registry identified hazelnut, walnut, and cashew as the cause of 73% of pediatric anaphylaxis cases across Germany, France, and Italy. The POSEIDON Phase 3 trial demonstrated a 68.4% desensitization rate to 1,000 mg of peanut protein in children aged 1-4 years, highlighting the significance of early-life intervention. Furthermore, real-world data from France associated sublingual immunotherapy with a 38% reduction in asthma risk, reinforcing its preventive potential.
In 2026, DBV Technologies submitted a Biologics License Application following positive VITESSE Phase 3 results, which demonstrated significant desensitization in children aged 4-7 years. In February 2024, Omalizumab became the first anti-IgE therapy approved for multiple food allergies, driving a shift in treatment guidelines toward the integration of biologics. Additionally, ALK-Abello's successful peanut-tablet Phase 2 results in April 2026 indicated further diversification in administration methods.
Omalizumab, a leading biologic therapy, is priced at over USD 2,000 per month. U.S. payers enforce prior-authorization requirements, including the submission of serum-IgE documentation and prescriptions from allergists. Medicare Part D beneficiaries face coinsurance rates of 25-33%, resulting in monthly out-of-pocket expenses ranging from USD 500 to 700. By 2025, 14 state Medicaid plans are expected to mandate step therapy through oral immunotherapy before approving biologics, potentially restricting access for low-income families.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Acute-care drugs, including epinephrine autoinjectors, antihistamines, and corticosteroids, accounted for 42.50% of 2025 revenue, highlighting their critical role in emergency management. The demand for epinephrine has been strengthened by the introduction of infant-dose products and affordable generics. However, disease-modifying agents, led by oral immunotherapy and omalizumab, are growing at an 8.88% CAGR, shifting the clinical focus from emergency interventions to preventive care. Guidelines emphasize that biologics are preventive in nature and should not replace epinephrine in acute situations.
Walnuts captured 28.55% of the 2025 segment revenue, reflecting their widespread use in baked goods and plant-based milks. Hazelnut oral immunotherapy achieved a high desensitization rate but provided minimal cross-protection to other nuts, underscoring the need for nut-specific treatment approaches. Rising cashew consumption in Asia is driving a 6.99% CAGR, with increasing demand for cashew-specific allergy treatments as exposure grows.
In 2025, North America secured 39.67% of the geographic revenue, driven by the United States' rapid adoption of omalizumab following its FDA approval in February 2024. This growth was supported by the widespread availability of epinephrine auto-injectors through retail and specialty pharmacies and a well-established network of allergy clinics providing Oral Immunotherapy (OIT). In January 2025, the American Academy of Allergy, Asthma & Immunology issued consensus guidance on omalizumab, standardizing patient selection criteria and dosing regimens. Additionally, the 2024 AAAAI-EAACI PRACTALL update aligned oral food challenge protocols, reducing variability across centers and facilitating multi-site clinical trials. Europe, accounting for approximately 28% of the market in 2025, saw Germany, the United Kingdom, France, Italy, and Spain leading in OIT adoption. However, a regulatory gap emerged as the European Medicines Agency's Committee for The EAACI 2024 guidelines recommended omalizumab and OIT for peanut allergies but highlighted limited evidence for tree nuts, which slowed reimbursement and broader adoption.
Asia-Pacific, experiencing a 7.90% CAGR through 2031, is driven by dietary westernization, which has increased tree nut consumption and sensitization rates. A 2025 study documented that eliciting doses for walnut and cashew in Japanese children are now approaching Western thresholds, attributed to rising nut consumption over the past decade. Additionally, China's tree nut import volume grew significantly between 2015 and 2024. The Middle East and Africa, led by Gulf Cooperation Council countries and South Africa, along with South America, anchored by Brazil and Argentina, collectively represent approximately 10% of the market. Growth in these regions is constrained by a limited number of specialists, low awareness of immunotherapy, and high out-of-pocket costs for biologics and diagnostics. However, urbanization and rising incomes are expected to narrow these gaps over the forecast period.