Phase 2 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:
- Adults aged 18 years or older
- People who have been diagnosed with chronic atopic dermatitis (eczema) for at least 6 months before the start of the trial, with the diagnosis confirmed by a photograph
- People whose eczema has not responded well enough to standard treatments (not including systemic immunosuppressants) used for at least 4 consecutive weeks within the past 6 to 12 months, or where a doctor has documented reasons why topical (skin-applied) treatments are not medically appropriate
- People with moderate to severe eczema, meaning a significant portion of the body's skin is affected, based on specific scoring measurements taken at both the screening and baseline appointments (confirm with trial site)
- People in the "bio-experienced" group — meaning those who have previously used biologic medicines (a type of injectable anti-inflammatory treatment) for at least 12 weeks within the past 5 years, and either had a partial or no response, experienced side effects or intolerances, or lost access to those treatments
- People with a body weight above 45 kg (100 lbs) and a body mass index (a measure of body weight relative to height) between 17.5 and 40
- People who are willing and able to attend all scheduled visits, follow the treatment plan, and complete all required tests and study procedures
Who may not be able to join:
- People with significant allergic or autoimmune conditions other than eczema, such as lupus or other complement disorders, Type 1 diabetes, inflammatory bowel disease, or multiple sclerosis (well-controlled mild to moderate cases may be considered — confirm with trial site)
- People with a history of severe allergic reactions, including anaphylaxis, or reactions to protein-based medicines, or known sensitivity to the specific study drugs being tested (people with allergies to a single identifiable, avoidable substance such as peanuts may still be considered if avoiding that substance during the study is possible — confirm with trial site)
- People with any active infection requiring treatment in the 2 weeks before screening, or who were hospitalised for an infection or received intravenous antibiotic treatment within 60 days before the trial start date
- People with an active skin infection requiring systemic antibiotic, antiviral, antifungal, or antiparasitic treatment within 2 weeks before the trial start date, or a surface-level skin infection requiring topical treatment within 1 week before the start date
- People who have had any infection considered serious or opportunistic within 6 months before the trial start date
- People with other inflammatory skin conditions (such as psoriasis, seborrheic dermatitis, or lupus affecting the skin) that could interfere with assessing eczema or the treatment's effects
- People with a medical or psychiatric condition, including recent or current thoughts of suicide or self-harm (within the past year), or abnormal laboratory results, that in the doctor's judgement could make participation unsafe or inappropriate
- People currently using any medications that are not permitted during the trial (confirm with trial site for the specific list)
- People who have had narrowband UVB phototherapy, broadband phototherapy, or regular use of a tanning bed (more than twice a week) within 4 weeks before the trial start date
- People who have taken part in another clinical trial involving an experimental medicine or vaccine within 30 days (or 5 half-lives of that medicine, whichever is longer) before the start of this trial
- People with HIV, hepatitis B, or hepatitis C infections, as determined by specific testing outlined in the trial protocol
- People with evidence of active or latent (inactive but present) tuberculosis (TB), or TB that has not been adequately treated; people currently being treated for active or latent TB are not eligible
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
Australian sites
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
4 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
The number of participants achieving ≥75% improvement in EAS175 from baseline at week16.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.