Phase 2 Psoriasis 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:
- People aged 18 to 75 years old at the time of screening, of any gender
- People who have been diagnosed with Generalized Pustular Psoriasis (GPP) based on specific criteria set by a 2017 international medical expert group (ERASPEN)
- People who are currently experiencing an acute (sudden/active) flare-up of GPP
- People who are able to read, understand, and are willing to sign a consent form agreeing to take part
- People who are willing to attend all required study visits and follow study procedures
- Women who are able to become pregnant must agree to use contraception throughout the study and for 6 months after the study ends
Who may not be able to join:
- People whose pustules (pus-filled skin spots) appear only on raised psoriasis plaques, rather than as the generalised (widespread) GPP pattern
- People who have another skin condition or other medical condition that might make it difficult for the study doctor to assess how well the treatment is working
- People who have a severe, worsening, or uncontrolled medical condition that the study doctor considers unsuitable for participation
- People who have abnormal blood test results for certain viruses during the screening period
- People whose chest X-ray shows active tuberculosis (TB), who have had close contact with someone with active TB in the past 6 months, or who test positive on a specific TB blood test (IGRA)
- People who were hospitalised due to a serious infection in the 2 months before the study start
- People who, in the study doctor's assessment, needed antibiotics, antifungal, or antiviral medicines taken throughout the body (not just on the skin) within 2 weeks before the study start
- People who have had a rare or unusual ("opportunistic") infection in the 6 months before the study start
- People who received a live or weakened live vaccine within 12 weeks before the study start
- People who had a major surgical procedure within 4 weeks before the study start, or who have a major surgery planned during the study period
- People who received a blood transfusion within 4 weeks before the study start
- People who took part in another clinical trial of a drug or medical device within 4 weeks before the study start
- People who have a known or suspected condition — present from birth or developed later — that weakens the immune system
- People who have any currently active cancer, or who have a history of cancer of any type
- People with alcohol dependence, drug dependence, or known dependence on any specific medicine
- Women who are pregnant or currently breastfeeding
- People who are unable to tolerate receiving medicine through an intravenous (IV) drip into a vein
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
Phone: 13693058190
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
Percentage of patients with a score of 0 for the pustule subterm
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.