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DBV Technologies to Present Data on VIASKIN® Peanut at AAAAI 2026

DBV Technologies announces that it will present additional data from the phase 3 VITESSE study on the VIASKIN® Peanut patch in children aged 4 to 7 at the 2026 annual meeting of the American Academy of Allergy, Asthma, and Immunology. The company will also host a product forum focused on the potential of epicutaneous immunotherapy (EPIT) in treating food allergies.


DBV Technologies to Present Data on VIASKIN® Peanut at AAAAI 2026

Presentation Details

DBV Technologies will deliver an oral presentation titled 'VITESSE Phase 3 Study: Efficacy and Safety of Epicutaneous Immunotherapy in Peanut-Allergic Children 4 Through 7 Years of Age' at the 2026 AAAAI annual meeting, which will be held in Philadelphia, Pennsylvania, from February 27 to March 2, 2026. The company will also organize a product forum featuring a panel of allergists to discuss the potential of EPIT to re-educate the immune system in the case of food allergies, examine the impact of early intervention in children allergic to peanuts, and analyze how new therapeutic options enable a more proactive approach to managing this allergy.

Exhibition Details

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DBV Technologies will be located at booth #1527 in the exhibition hall of the AAAAI, where attendees can receive information about epicutaneous immunotherapy and the VIASKIN® Peanut patch. The advanced-stage biopharmaceutical company focuses on developing treatment options for food allergies and other immune conditions. DBV Technologies is currently studying the use of its proprietary VIASKIN® patch technology to treat food allergies, with ongoing programs in young children aged 1 to 3 years and children aged 4 to 7 years who are allergic to peanuts.



Sector Pharmacie et biotechnologies Biotechnologies


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Context

Period
  • Period: S1 2026
Key reported figures
  • Revenue: 1,6 millions de dollars
  • Quarterly revenue: 1,6 millions de dollars
  • Net income: -98 millions de dollars
Guidance from the release
  • DBV is a late-stage biopharmaceutical company currently in regulatory discussions with the FDA, with BLA submission anticipated in Q3 2026; the company reports cash funding into Q3 2027, indicating reliance on capital reserves and no current revenue generation.

The information presented in this article is provided for informational purposes only and does not constitute an investment recommendation, an incentive to buy or sell a financial asset, or investment advice. Readers are invited to conduct their own research before making any decision.

Investments in the stock market involve risks, including the risk of capital loss. Past performance of an asset or market is no guarantee of future results. Any investment decision should be made taking into account your personal financial situation, objectives and risk tolerance.

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