Eczema Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are 12 years old or older and have been diagnosed with moderate to severe atopic dermatitis (a serious form of eczema) that has needed whole-body (systemic) treatments in the past
- Your doctor has decided that starting treatment with Cibinqo (abrocitinib) tablets is appropriate for you
- You (or your parent or legal guardian, if applicable) are willing and able to sign and date a consent form after being fully informed about the study
Who may not be able to join:
- You have already been treated with Cibinqo tablets before
- You are currently taking part in another clinical study that involves a treatment or experimental medicine
- Your blood test results show that your platelet count, white blood cell count, lymphocyte count, or haemoglobin (red blood cell level) are below certain safe levels (confirm with trial site)
- You have had an allergic reaction to Cibinqo or any of its ingredients
- You currently have a serious active infection, including tuberculosis (TB)
- You have severe liver problems
- You are pregnant or breastfeeding
- You have a rare inherited condition affecting how your body handles certain sugars, such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Pfizer CT.gov Call Center, Pfizer
Phone: 1-800-718-1021
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Number of participants with Adverse Events (AE's) according to frequency; Number of participants with Adverse Drug Reactions (ADR's) according to frequency; Number of participants with unexpected AE's according to frequency; Number of participants with unexpected ADR's according to frequency; Number of participants with Serious Adverse Events (SAE's) according to frequency; Number of participants with Serious Adverse Drug Reactions (SADR's) according to frequency; Number of participants with Adverse Events of Special Interest (AESI) according to frequency
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.