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HomeEfficacy

Phase 3 Study Primary Endpoints

Success in ISGA: Clear or almost clearStudy Design

Phase 3 Study Secondary and Other Endpoints

ISGA clear or almost clearTime to ISGA success
Phase 3 Study: Other EndpointsPruritusQuality of life assessmentsInfant Study: Exploratory EndpointsISGA clear or almost clear%BSA, EASI & POEM52-Week Trial
Safety DataSafety DataPhase 3 Study Adverse Reactions*Pivotal trial & 48-week extension study Adverse ReactionsOpen-Label Safety Extension Study*Open-Label Safety Extension Study Rescue Therapy EndpointStudy designInfant Safety Study**Adverse ReactionsStudy design and Demographics52-Week TrialReal PatientsReal patient case reportsReal patient case studiesNana's experience with EucrisaBraxton's testimonialHand and fingerFace and neckOtherHand and finger5-yr-old Caucasian female - hands8-yr-old Caucasian female - hands15-yr-old Caucasian male - hand55-yr-old Caucasian female - hand64-yr-old Caucasian female - thumb70-yr-old Caucasian male - thumbFace and neck15-yr-old Caucasian male - chin18-yr-old Hispanic female - face and neck75-yr-old Caucasian male - faceOther39-yr-old Asian male - arm44-yr-old African American female - legs72-yr-old Caucasian female - legDosingSavings & SupportSavings & SupportEventsMaterialsVideosCopay CardsCost and Coverage
Prescribing InformationPatient Information Indication Patient Site

NEW! 52-week data and FDA-approved with a once-daily dosing option.1

NEW! 52-week data and
FDA-approved with a once-daily dosing option.1

Please see Full Prescribing Information for details.

EUCRISA (crisaborole): A steroid-free optionFor the treatment of mild-to-moderate atopic dermatitis in patients 3 months and older Proven Efficacy

Steroid-free EUCRISA provides efficacy and can be used as part of a long-term treatment plan1,2

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Dosing Options

EUCRISA has a dosing regimen that can be adjusted to fit your patient's needs1

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Established Safety Profile

EUCRISA has safety data across 5 studies, including pivotal and open-label safety extension studies, and an open-label infant safety study1,3

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Dosing

EUCRISA is now FDA-approved with an expanded dosing recommendation to consider once-daily application once clinical effect has been achieved with twice-daily application1

EUCRISA is now
FDA-approved with an expanded dosing recommendation to consider once-daily application once clinical effect has been achieved with twice-daily application1

EUCRISA is now
FDA-approved with an expanded dosing recommendation to consider once-daily application once clinical effect has been achieved with twice-daily application1

See Full Prescribing Information
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“Sometimes I don’t even want to look at my own skin”

Nana is a dancer who has had mild-to-moderate atopic dermatitis for more than 30 years

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Cost & Coverage

EUCRISA is covered for approximately 95% of commercially-insured lives. Check the cost and coverage options in your area

EUCRISA is now
FDA-approved with an expanded dosing recommendation to consider once-daily application once clinical effect has been achieved with twice-daily application1

EUCRISA is covered for approximately 95% of commercially-insured lives. Check the cost and coverage options in your area

See options
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Infant Safety Study

Learn more about a 28-day, single-arm, open-label study in 3 to <24 month old patients2

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Copay Cards

*Eligible patients pay as little as $10

Download Copay Cards LoadingPatients 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.
Safety Data in patients 2 years and older

Learn more about the safety data of EUCRISA from the 4-week pivotal trials and open-label safety extension study1,2

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Efficacy

EUCRISA has proven efficacy across all pivotal trial primary and secondary endpoints in patients aged 2 years and up1,3

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Infant Safety Study in patients 3 to <24 months of age

Learn more about a 28-day, single-arm, open-label safety study in 3- to <24-month-old patients 4

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ReferencesEUCRISA® (crisaborole) Full Prescribing Information. April 2023.Schlessinger J, Shepard JS, Gower R, et al. Safety, effectiveness, and pharmacokinetics of crisaborole in infants aged 3 to <24 months with mild-to-moderate atopic dermatitis: a phase IV open-label study (CrisADe CARE 1). Am J Clin Dermatol. 2020;21:275-284.Eichenfield LF, Call RS, Forsha DW, et al. Long-term safety of crisaborole ointment 2% in children and adults with mild to moderate atopic dermatitis. J Am Acad Dermatol. 2017;77(4):641-649.e5.

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PP-EUC-USA-0066
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PP-EUC-USA-0032
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.

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.
Important Safety Information

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

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