Taking people in GermanyPhase 4
Tests guselkumab on enthesitis in people with psoriatic arthritis
Tests guselkumab to see if painful tendon attachment inflammation settles in adults with psoriatic arthritis.
Key facts
- Who runs it
- Universitaetsklinikum Erlangen AöR
- Where
- Berlin, Cologne, Erlangen, and Frankfurt Am Main, GermanySee the 4 sites
- Trial code
- Registry title
- Prospective, multicentre, open-label clinical trial on the effect of GUSelkumab on the resolution of ultrasound-proven ENThEsitis in patients with pSoriatic arthriTis
- Status
- Recruiting
- Phase
- Phase 4
- People taking part
- 78 people, planned
- Started
- 13 Sept 2024
- Expected to end
- 31 Dec 2027
- Type of study
- Interventional
- Record updated
- 3 June 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with psoriatic arthritis who have inflammation where tendons attach to bone (enthesitis), confirmed on ultrasound. They will receive guselkumab.
- Age
- 18 years or older
- Sex
- Men and women
- Disease stage
- Psoriatic arthritis (CASPAR criteria) with enthesitis: SPARCC Enthesitis score of at least 1, and ultrasound (PD) Grade 2 or more in at least 1 enthesis, or Grade 1 or more in at least 2 entheses.
- Earlier treatment
- No earlier biologic DMARD, or no more than one earlier TNF inhibitor. Must have had failure of or a bad reaction to at least one csDMARD, or need to start systemic therapy with Guselkumab because of moderate-to-severe plaque psoriasis.
Main reasons for not taking part
- Another rheumatological or immune disease, such as rheumatoid arthritis, SLE or Behcet syndrome
- Ongoing, long-lasting or repeated infection (HIV, HBV or HCV) or tuberculosis infection
- Any cancer, or lymphoproliferative disease, in the past 5 years (a few treated minor types excepted)
- Alcohol or drug abuse in the last six months
- Pregnant or breastfeeding women
The registry criteria, word for word
Show all 15 criteriaShow less
Who can take part
- Written informed consent obtained from the subject
- Adult male or female subject; age ≥ 18 years
- Diagnosis of PsA according to CASPAR criteria
- SPARCC Enthesitis ≥ 1 at baseline
- bDMARD naïve or previous treatment with no more than one TNFi
- Failure or adverse reaction to at least one csDMARD or indication to start systemic therapy with Guselkumab due to moderate-to-severe plaques psoriasis
- PD Grade ≥ 2 for at least 1 affected enthesis at baseline or PD Grade ≥ 1 for at least 2 affected entheses at baseline
Who cannot take part
- Concomitant florid active immune mediated disease (e.g. autoimmune hepatitis) that is untreated and/or requires immunosuppressive treatment
- History or evidence of ongoing alcohol or drug abuse, within the last six months prior to enrolment
- Use of any inadmissible medication (e.g. drugs under development or bDMARDs approved for PsA other than Guselkumab) List of admitted drugs alongside IMP: • csDMARD - Leflunomide (e.g. Arava), Sulfasalazine (e.g. Azulfidine RA, Pleon RA), Methotrexate (e.g. Lantarel, Metex) and/or • systemic glucocorticoids with a stable dose of ≤ 7,5 mg of prednisolone equivalents within the last 12 weeks of screening
- Diagnosis of any other rheumatological/ immunological disease such as rheumatoid arthritis, SLE, PSS, MCTD, Behcet syndrome or GPA
- History of ongoing, chronic or recurrent infectious disease (Infection with HIV, HBV or HCV) or evidence of tuberculosis infection as defined by a positive QuantiFERON Tb-Gold test. If presence of latent tuberculosis is established then treatment according to local country guidelines must have been initiated but patient cannot take part in the study
- History of lymphoproliferative disease or any known malignancy or history of malignancy of any organ system (except for basal cell carcinoma or actinic keratosis that have been treated with no evidence of recurrence in the past 3 months, carcinoma in situ of the cervix or non-invasive malignant colon polyps that have been removed), treated or untreated within the past 5 years prior to enrolment
- Contraindication for Guselkumab treatment according to their SmPCs
- Nursing mother or pregnant woman
Where in Germany
- Charite Universitaetsmedizin Berlin KöRBerlin, GermanyTaking people
- Krankenhaus Porz am Rhein gGmbHCologne, GermanyTaking people
- Universitaetsklinikum Erlangen AöRErlangen, GermanyTaking people
- Fraunhofer Institute For Translational Medicine And Pharmacology ITMPFrankfurt Am Main, GermanyTaking people
About the trial
What the trial wants to find out
To assess the effect of Guselkumab on the resolution of clinical and ultrasound-confirmed enthesitis in patients with PsA
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- Prospective, multicentre, open-label clinical trial on the effect of GUSelkumab on the resolution of ultrasound-proven ENThEsitis in patients with pSoriatic arthriTis
- Plain-language title
- Tests guselkumab on enthesitis in people with psoriatic arthritisGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 9 November 2026.
- Record updated
- 3 June 2026