• Prescribing Information
  • Patient Information
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  • Phase III Study Primary Endpoint*
    Phase III Study Secondary Endpoints*
    Phase III Study: Other Endpoints*
    Infant Study: Exploratory Endpoint**

    *Phase III pivotal studies and open-label safety extension study investigated in patients 2 years and older

    **Infant study investigated patients aged 3 to <24 months

    *Phase III pivotal studies and open-label safety extension study investigated in patients 2 years and older

    **Infant study investigated patients aged 3 to <24 months

    EUCRISA Dosing

    EUCRISA can be applied to the skin anywhere on the face and body1

    EUCRISA is for topical use only and not for ophthalmic, oral, or intravaginal use1

    Apply a thin layer of EUCRISA twice daily to affected areas of the skin1

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    No limitations on duration of use1

    If signs and symptoms of hypersensitivity occur, discontinue EUCRISA immediately and initiate appropriate therapy

    EUCRISA was studied in pivotal trials for 29 days and in an open-label safety extension study for up to 48 weeks

    Studied as monotherapy in treatment-naïve and treatment-experienced patients2*

       *Patients involved in pivotal trials were not required to have received prior treatment for atopic dermatitis. Those who did went through a washout period before starting treatment with EUCRISA.2

    Mean BSA of 18.3% in pivotal trials2

    Can be used on all skin tones2

       *Patients involved in pivotal trials were not required to have received prior treatment for atopic dermatitis. Those who did went through a washout period before starting treatment with EUCRISA.2

     References
    1. EUCRISA® (crisaborole) Full Prescribing Information. December 2018.
    2. Data on file. Pfizer Inc., New York, NY.
    3. Eichenfield LF, et al. J Am Acad Dermatol. 2017;77(4):641-649.​​​​​​​​​​​​

    Patient Information

    Help your patients by setting expectations

    Download here

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    Learn how the first and only nonsteroidal topical PDE4 inhibitor works within the skin1

    The specific mechanism(s) of action of crisaborole in atopic dermatitis is not well defined. PDE4=phosphodiesterase 4

    Learn more

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    Copay Cards

    *Eligible patients pay as little as $10​​​​​​

    Terms and Conditions apply​​​​​​

    ​​​​* Patients enrolled in state or federally funded prescription insurance programs are not eligible to use this card. Savings up to $970 per tube. Annual savings up to $3,880. This card will be accepted only at participating pharmacies. This card is not health insurance.

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    Savings & Support Program

    A savings and support program for your patients to help them with their access to EUCRISA

    See resources

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    Order Samples

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    Contraindications

    EUCRISA is contraindicated in patients with known hypersensitivity to crisaborole or any component of the formulation.

    Warnings and Precautions

    Hypersensitivity reactions, including contact urticaria, have occurred in patients treated with EUCRISA and should be suspected in the event of severe pruritus, swelling, and erythema at the application site or at a distant site. Discontinue EUCRISA immediately and initiate appropriate therapy if signs and symptoms of hypersensitivity occur.

    Adverse Reactions

    The most common treatment-related adverse reaction occurring in clinical trials was application site pain, such as burning or stinging.

    Please see Full Prescribing Information and Patient Information

    EUCRISA is indicated for topical treatment of mild-to-moderate atopic dermatitis in adult and pediatric patients 3 months of age and older.

    INDICATION

    EUCRISA (crisaborole) is indicated for topical treatment of mild‑to‑moderate atopic dermatitis in adult and pediatric patients 3 months of age and older.

    EUCRISA is for topical use only and is not for ophthalmic, oral, or intravaginal use. For more information, please view the full prescribing information here.