Clareo Health | The Purpose of This Study is to Evaluate the Effects of Ruxolitinib Cream on Adults With Atopic Dermatitis Experiencing Sleep Disturbance.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Incyte Corporation
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Has clinically confirmed diagnosis of active AD according to Hanifin and Rajka (1980) criteria.
Has at least a 2-year history of AD (information obtained from medical chart, participant's physician, or directly from the participant).
Has an overall BSA affected by AD of 3%-20% (excluding scalp) at the screening and baseline visits.
Has an IGA score ≥ 2 at the screening and baseline visits.
Has an Itch NRS score ≥ 4 at the screening and baseline visits.
Willing to complete the once-daily Itch NRS (24-hour recall period) entries at approximately the same time each day during the study.
Agrees to maintain a regular sleep schedule during the study period.
Willing and able to follow required study procedures for measuring sleep for the duration of the study.
You may not be if
Currently using a wearable or other device for monitoring sleep patterns and unwilling to discontinue its use during the study.
Currently has a schedule that includes nighttime work shifts.
Has had significant flares or unstable course in AD (ie, condition worsened significantly or required significant change in medications, as per medical judgment) in the previous 4 weeks before screening (information obtained from medical chart, participant's physician, or directly from the participant).
Has received any ultraviolet B phototherapy (including tanning beds) or excimer laser within 4 weeks prior to the screening period.
Has had psoralen plus ultraviolet A treatment within 4 weeks prior to the screening period.
Has received a nonbiological investigational product or device within 4 weeks prior to the screening period, or is currently enrolled in another investigational drug study.
Has received treatment with JAK inhibitors (systemic or topical) within 4 weeks prior to the screening period.
Has had prior treatment with a JAK inhibitor that was discontinued for safety reasons or tolerance problems.
Has a known or suspected allergy to ruxolitinib or any component of the study drug.
