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Phase 3 Study: Primary Endpoints
Phase 3 Study: Secondary and Other Endpoints
Pooled results from 2 pivotal studies in patients 2 years and older.3
Baseline scores of both the DLQI and the CDLQI in the pivotal trials reflect a moderate effect of atopic dermatitis on patient lives.4-6
Composite scores are based on a scale of 0-30.4-6
The higher the score, the greater the impairment of QoL.7
MCID (or MID, as it is sometimes referred to) is the smallest difference in score that suggests there has actually been a meaningful change in studied patients’ quality of life since the previous measurement of his/her scores that would lead the patient or clinician to consider a change in management.8,9
CDLQI is validated for use in children 4-16 years of age and can be completed with the help of the child's parent or guardian. The data presented includes patients 2-15 years of age. These results are consistent with the findings of a subgroup analysis in patients 4-15 years of age.6
Find out more about the proportion of patients aged 2 years and older who achieved ISGA Clear or Almost Clear at Day 29 as a Phase 3 trial's secondary endpoint
Learn more about 28-day, open-label, single-arm, safety study in 3 to <24-month-old patients14
Find out more about the proportion of patients who achieved Clear or Almost Clear at Day 29 in the primary endpoint
*Eligible patients pay as little as $10
A savings and support program for your eligible patients to help them with their access to EUCRISA*
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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.
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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.