Phase 2 Eczema Trial, Recruiting NCT05995964 Sponsor: Pfizer Condition: Eczema
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Phase 2 Eczema Trial, Recruiting

NCT05995964
Recruiting Phase 2 🇦🇺 Australian site

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Pfizer CT.gov Call Center, Pfizer

Phone: 1-800-718-1021

Australian sites

Australian Clinical Research Network, Sydney, New South Wales
Box Hill Hospital, Box Hill, Victoria
Sinclair Dermatology, East Melbourne, Victoria
Fremantle Dermatology, Fremantle, Western Australia

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

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
22 August 2023
Est. completion
19 October 2026

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇨🇳 China 🇩🇪 Germany 🇯🇵 Japan 🇵🇱 Poland 🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov