Description
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Randomised double-blinded study
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2 study groups
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Ruxolitinib cream 1.5%
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Vehicle cream
-
-
Participants randomised into the vehicle cream treatment arm will be allowed to enter the ruxolitinib 1.5% cream open-label escape arm after 8 weeks if treatment is inadequate.
Trial length
34 Weeks
Participant age
Participant ages can range from 18 and above
Patient eligibility
-
Participants must have atopic dermatitis (AD) for 2 or more years
-
Participants must have moderate AD
-
Participants must have history (within 12 months before the screening visit) of inadequate response, intolerance, or contraindication to topical corticosteroids and topical calcineurin inhibitors
-
Female participants must NOT be pregnant
10 onsite visits are required from patients
*Travel is reimbursed for each visit
Follow-up inclusions
Objectives
To establish the efficacy of ruxolitinib cream in participants with moderate AD who had an inadequate response to topical corticosteroids and topical calcineurin inhibitors.
Description
-
Randomised double-blinded study
-
2 study groups
-
Ruxolitinib cream 1.5%
-
Vehicle cream
-
-
Participants randomised into the vehicle cream treatment arm will be allowed to enter the ruxolitinib 1.5% cream open-label escape arm after 8 weeks if treatment is inadequate.
Trial length
34 weeks
Participant age
Participant ages can range from 18 and above.
Patient eligibility
-
Participants must have atopic dermatitis (AD) for 2 or more years
-
Participants must have moderate AD
-
Participants must have history (within 12 months before the screening visit) of inadequate response, intolerance, or contraindication to topical corticosteroids and topical calcineurin inhibitors
-
Female participants must NOT be pregnant
10 onsite visits are required from patients
*Travel is reimbursed for each visit
Follow-up inclusions
Objectives
To establish the efficacy of ruxolitinib cream in participants with moderate AD who had an inadequate response to topical corticosteroids and topical calcineurin inhibitors.
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