Adults aged 18 and older with a diagnosis of moderate or severe atopic dermatitis (AD) may be eligible for a clinical trial. Eligible participants
must be starting upadacitinib treatment (per local label), prior to and independently of enrolment in the study. Individuals must have had previous AD (eczema) treatment with dupilumab, which was sub-optimally controlled or discontinued due to safety/tolerability reason(s).
Participants will be taking oral upadacitinib treatment (per local label). Study-related assessments will be provided. Reimbursement for studyrelated expenses may be provided.
Study participation will last approximately 4 months and involve up to 4 visits to the study centre.
The following information is from ClinicalTrials.gov
Last Update Posted: September 24, 2023
Atopic dermatitis (AD) is a skin condition that may cause a rash and itching due to inflammation of the skin. Therapies spread over the skin may not be enough to control the AD in trial participants who require systemic anti-inflammatory treatment. This study will assess the real-world effectiveness of upadacitinib on adult participants with moderate-to-severe AD who are inadequate responders to dupilumab or who are discontinuing from dupilumab due to safety/tolerability reasons. This study also aims to understand upadacitinib utilization patterns in real-world clinical practice. In Canada, upadacitinib is indicated for the treatment of adults and adolescents 12 years of age and older with refractory moderate to severe atopic dermatitis (AD) who are not adequately controlled with a systemic treatment (e.g., steroid or biologic) or when use of those therapies is inadvisable. CAN UpTIMISE will enroll approximately 100 adult participants, 18 years of age and above, with moderate-to-severe AD who are inadequate responders to dupilumab or are discontinuing from dupilumab from up to 25 sites in Canada. Participants will receive oral upadacitinib tablets as prescribed by the physician prior to enrolling in this study in accordance with the terms of the local marketing authorization and professional and reimbursement guidelines with regards to dose, population, and indication. The overall duration of the study is approximately 4 Months. Participants will attend regular visits per routine clinical practice. The effect of the treatment will be checked by medical assessments, using questionnaires, and reporting potential side-effects.
Condition or Disease:
Ages Eligible for Study:
18 Years and older (Adult)
Sexes Eligible for Study:
Able to give written informed consent before starting any study-related assessments
Diagnosis of moderate or severe AD, as per investigator’s judgement
Initiating upadacitinib treatment, as per the local label, and where decision to treat with upadacitinib must have been made with the participant, prior to and independently of enrolment in the study
Previous treatment with dupilumab for AD, as the most recent systemic therapy, and who is either or:
i. sub-optimally controlled as per investigator judgement, after at least 16 weeks of dupilumab treatment, with or without additional AD therapies, at time of baseline visit.
ii. discontinuing dupilumab due to safety/tolerability reason(s) as per investigator judgement at the baseline visit
Availability of medication history during the past 4 weeks prior to baseline visit
Previous treatment with any systemic JAKi including upadacitinib, or any investigational drug of chemical or biologic nature within 4 weeks or five half-lives of the drug (whichever is longer) prior to and at the time of the baseline visit
Currently enrolled in an interventional clinical study, or within the last 30 days or five-half lives of being administered an investigational drug, whichever is longer, prior to baseline visit. Participation in other observational studies or registries is acceptable.
Terms and Conditions – ClinicalTrials.gov
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