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Phase 3 Study Primary Endpoints
Phase 3 Study Secondary and Other Endpoints
Actual 70-year-old patient treated with EUCRISA. Clinical studies of EUCRISA did not include sufficient numbers of subjects age 65 and over to determine whether they respond differently from younger subjects.
BEFORE: Day 1
AFTER: Day 28
Reason for Visit | Evaluation of recent onset scaling on right hand |
Initial Presentation |
|
Areas affected | Right thumb and fingers |
Medication prescribed | EUCRISA (crisaborole) ointment, 2%, twice daily |
Basic skin care instructions | Over-the-counter moisturizer |
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
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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