JPRN-UMIN000048463
Completed
未知
A Prospective Study to Evaluate Effectiveness of Upadacitinib in Moderate to Severe AD with Prurigo Nodules in the Real World in Japan - ADMIRE
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- AbbVie GK
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\. Patients who had prior treatment with Upadacitinib 2\.Patients who have contraindications to Upadacitinib 3\. Patients who have chronic pruritus resulting from another condition (e.g.,neuropathic disorders) than AD, prurigo nodules 4\. Patients who have prurigo nodules caused by medication, metal allergy, infection, insect bite 5\. Patients who are currently participating in interventional research or participated within 30 days (not including another post\-marketing observational study, or registry participation).
Outcomes
Primary Outcomes
Not specified
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