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Phase 3 Study Primary Endpoints
Phase 3 Study Secondary and Other Endpoints
15-year-old Caucasian male with mild-to-moderate atopic dermatitis
3 Week
4 Week
Tab Number 5
Day 1
3 Week
Day 1
4 Week
Reason for Visit | Evaluation of AD |
Initial Presentation | Lesion – Itching and skin rash left dorsum hand, right palm |
Areas affected | Dorsum of left hand; palm of right hand |
Medication prescribed | EUCRISA (crisaborole) ointment, 2%, twice daily |
Basic skin care instructions | Counseling on moisturizers and lotions and long-term skin care |
Clinical course | Clinical improvement seen at 3- and 4-week follow-up after commencing EUCRISA |
Hear JP with mild-to-moderate AD explain what EUCRISA means to him and other babies like him
Not an actual patient
The specific mechanism(s) of action of crisaborole in atopic dermatitis is not well defined. PDE4=phosphodiesterase 4
*Eligible patients pay as little as $10
A savings and support program for your patients to help them with their access to EUCRISA
Register or sign in to check availability and request samples.
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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.
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