NCT07887867Not yet recruiting
A Study to Learn About the Study Medicine Abrocitinib in People With Severe Atopic Dermatitis Who Have Switched From Other Therapies
A REAL-WORLD RETRO-PROSPECTIVE SINGLE COHORT STUDY EVALUATING THE EFFECTIVENESS OF ABROCITINIB (100/200 MG) IN PATIENTS AFFECTED BY SEVERE ATOPIC DERMATITIS SWITCHED PER CLINICAL PRACTICE FROM OTHER ADVANCED THERAPIES, INCLUDING BIOLOGICS AND/OR OTHER JAK INHIBITORS - ABRO-SWITCH
Source: ClinicalTrials.gov · Last updated 21 Oct 2026
Brief summary (registry, in English)
The purpose of this observational study is to learn about the effects of the study medicine (called abrocitinib) for the treatment of severe atopic dermatitis in people that were moved from previous novel therapies, known as "advanced" therapies. Atopic dermatitis is a long-lasting skin condition that causes the skin to become inflamed, dry, and itchy. This study is seeking participants who: * are 18 years of age or older; * have severe atopic dermatitis; * have previously been treated with advanced therapies authorised for atopic dermatitis and are moving to abrocitinib (100 mg or 200 mg); * have received no more than two authorised advanced therapies for their atopic dermatitis. All participants will receive study medicine, abrocitinib as part of their usual medical care. The decision to give the study medicine is made by their dermatologist. This decision is independent of participation in the study. Abrocitinib will be taken by mouth at home once daily as prescribed by the treating doctor. We will examine the experiences of people receiving abrocitinib for up to one year after starting abrocitinib. We will look back at the information up to 6 months before they have started taking abrocitinib. This will help us learn how abrocitinib affects severe atopic dermatitis in people who have moved from other authorised advanced therapies. Participants will take part in this study for 1 year. During this time, they will have about 5 visits. These visits are a part of their routine care. During the visits, the doctor will assess how severe atopic dermatitis is. Participants may be asked questions about their symptoms and how the condition affects their daily life. No additional clinic visits, tests, or procedures are required for this study, beyond normal clinical practice.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 120 (estimated)
- First submitted
- 29 Sept 2026
- Start date
- 1 Oct 2026
- Primary completion date
- 1 Oct 2027
- Lead sponsor
- Pfizer
- Diseases
- Atopic dermatitis (eczema)
- NCT number
- NCT07887867
What you commit to
- Study type: Observational
- Planned participants: 120
- From 1 Oct 2026 to the primary completion date, 1 Oct 2027
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Who the study is looking for
- \>=18 years of age on date of the enrolment visit
- Severe atopic dermatitis diagnosed in accordance with guidelines used per clinical practice
- Patients have agreed to switch from a prior advanced therapy for severe AD (i.e., dupilumab, lebrikizumab, tralokinumab, baricitinib, or upadacitinib) to abrocitinib 100 mg or 200 mg, based on the Investigator's clinical judgment and independent of study participation.
- Evidence of a personally signed and dated informed consent document
- Exclusion Criterion: Patients treated with more than 2 advanced therapies for AD, either biologics or JAKis
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.