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     Quick Explanation



    Assuming U.S. FDA approvals, dupilumab (Dupixent) has six disease indications as of August 25, 2026: atopic dermatitis (2017), asthma (2018), chronic rhinosinusitis with nasal polyps (2019), eosinophilic esophagitis (2022), prurigo nodularis (2022), and COPD with an eosinophilic phenotype (2025). The dates below are the original FDA approval dates, not later age-range or labeling expansions.


     Long Explanation



    U.S. FDA indication timeline

    IndicationOriginal approval
    Moderate-to-severe atopic dermatitisMarch 28, 2017
    Moderate-to-severe eosinophilic asthmaOctober 19, 2018
    Chronic rhinosinusitis with nasal polypsJune 26, 2019
    Eosinophilic esophagitisMay 20, 2022
    Prurigo nodularisSeptember 27, 2022
    COPD with an eosinophilic phenotypeMay 2025

    The first five dates are documented in FDA approval announcements or FDA approval records: atopic dermatitis ; asthma ; nasal polyps ; eosinophilic esophagitis ; and prurigo nodularis . The COPD indication was approved by FDA in 2025 for adults with inadequately controlled COPD and an eosinophilic phenotype; the FDA communication and current label support the year, but the exact approval-day date should be checked against the dated FDA approval letter or updated Drugs@FDA record before citing a day-level date.

    Scope: This is the U.S. FDA disease-indication timeline. European Union, United Kingdom, and other jurisdictions can have different dates, wording, age limits, and regulatory status. Later pediatric approvals and label expansions are intentionally not counted as new disease indications. Confidence is high for the first five dates and the six-indication list; confidence is moderate for the COPD month/day because the accessible regulatory label establishes the indication but not a complete historical chronology.



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    Updated: August 25, 2026

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