New pill for eczema tested in over 1,000 japanese patients
NCT ID NCT05387980
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tracks the safety and effectiveness of CIBINQO (abrocitinib) tablets in over 1,100 Japanese patients with atopic dermatitis (eczema) under real-world medical practice. Researchers will monitor side effects, treatment dropouts, and skin clearance over time. The goal is to see how well the drug works outside of strict clinical trial settings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CIBINQO (abrocitinib) tablets
- What this could lead to
- If successful, this study could confirm that CIBINQO is a safe and effective option for controlling atopic dermatitis in Japanese patients.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be less definitive. Side effects and treatment discontinuation are being tracked, and not all patients may benefit.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
1,128 people
The number who actually took part.
- Started
-
Apr 2022
- Expected to finish
-
Nov 2028
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adolescent participants diagnosed with atopic dermatitis in Japan.
- Ages
-
12 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Participants receiving this Product for treatment of AD. 2. Participants start receiving this Product (commercial product) for the first time and no earlier than the contract date of this Study, or Participants who continues to receive this drug after hospital transfer can be registered retrospectively. Exclusion Criteria: 1\. Participants previously enrolled in this Study at the same site.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Pfizer Local Country Office
Tokyo, Japan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can an eczema drug reshape the Skin's microbial community?