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Taking people in FranceNo phase

Follows adults with psoriatic arthritis treated with risankizumab over time

Observes how long adults with psoriatic arthritis stay on risankizumab compared with other treatments.

Plain-language title generated from the registry record
Registry title: An Ex-US Study to Assess Treatment Persistence With Risankizumab in Adult Participants With Psoriatic Arthritis

Key facts

Where
Aix-en-Provence, Arras, Besançon, Boulogne-sur-Mer, Cahors, Caluire-et-Cuire, Cannes, Chambray-lès-Tours, Clermont-Ferrand, Corbeil-Essonnes, Créteil, Échirolles, Lille, Limoges, Montauban, Montpellier, Nantes, Nice, Orléans, Paris, Péronne, Rennes, Rouen, and Valenciennes, FranceSee the 27 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT06764693, who can take part

Where in France

  • Hôpital Privé De Provence /ID# 275797Aix-en-Provence, FranceTaking people
  • Centre Hospitalier D'Arras /ID# 275192Arras, FranceTaking people
  • Centre Hospitalier Regional Universitaire de Besancon - Hopital Jean Minjoz /ID# 277881Besançon, FranceTaking people
  • Centre Hospitalier Boulogne-Sur-Mer /ID# 277269Boulogne-sur-Mer, FranceTaking people
  • CH de Cahors /ID# 275092Cahors, FranceTaking people
  • Infirmerie Protestante De Lyon /ID# 274922Caluire-et-Cuire, FranceTaking people
  • Centre Hospitalier De Cannes - Hôpital De Cannes /ID# 275193Cannes, FranceTaking people
  • Centre Hospitalier Régional Universitaire De Tours - Hôpital Trousseau /ID# 275397Chambray-lès-Tours, FranceTaking people
  • Centre Hospitalier Universitaire Gabriel-Montpied /ID# 275399Clermont-Ferrand, FranceTaking people
  • Centre Hospitalier Sud Francilien /ID# 275038Corbeil-Essonnes, FranceTaking people
  • Henri Mondor Hospital /ID# 275360Créteil, FranceTaking people
  • Chu Grenoble - Hôpital Sud /ID# 275200Échirolles, FranceTaking people
  • CHU de Lille - Hôpital Salengro /ID# 274980Lille, FranceTaking people
  • CHU Limoges - Dupuytren 2 /ID# 274918Limoges, FranceTaking people
  • Clinique François Chénieux /ID# 276516Limoges, FranceTaking people
  • Pôle Santé du Pont de Chaume /ID# 275608Montauban, FranceTaking people
  • Chu Montpellier /ID# 274925Montpellier, FranceTaking people
  • Centre Hospitalier Universitaire de Nantes, Hotel Dieu -HME /ID# 275396Nantes, FranceTaking people
  • Centre Hospitalier Universitaire de Nice - Hopital Pasteur /ID# 274923Nice, FranceTaking people
  • Centre Hospitalier Régional d'Orléans - Hôpital de la Source /ID# 275377Orléans, FranceTaking people
  • AP-HP - Groupe Hospitalier 10e - Hopital Lariboisiere /ID# 275182Paris, FranceTaking people
  • Groupe Hospitalier Paris Saint-Joseph /ID# 274981Paris, FranceTaking people
  • Hopital Pitie Salpetriere /ID# 275368Paris, FranceTaking people
  • Cabinet libéral du Dr PAUPIERE /ID# 275401Péronne, FranceTaking people
  • Chru De Rennes - Hôpital Sud /ID# 277115Rennes, FranceTaking people
  • Centre Hospitalier Universitaire de Rouen (CHU)- Hopital Charles Nicolle /ID# 275366Rouen, FranceTaking people
  • Centre Hospitalier de Valenciennes /ID# 276354Valenciennes, FranceTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
AbbVie
Trial code
NCT06764693
Record updated
17 February 2026
Original description
Psoriatic arthritis (PsA) is a type of arthritis (swelling and stiffness in the joints) that is frequently seen in trial participants who also have the skin condition psoriasis. It is caused by an overactive immune system where the body attacks healthy tissue by mistake. This study aims to describe the long term usage and effectiveness with risankizumab (RZB) relative to other advanced therapeutic options for the management of PsA in daily clinical practice.Read full original descriptionShow less

Prospective Multi-country, Real-world, Multi-arm Study of Treatment PErsistence With RISankizumab in Psoriatic Arthritis (PERIS)

Psoriatic arthritis (PsA) is a type of arthritis (swelling and stiffness in the joints) that is frequently seen in trial participants who also have the skin condition psoriasis. It is caused by an overactive immune system where the body attacks healthy tissue by mistake. This study aims to describe the long term usage and effectiveness with risankizumab (RZB) relative to other advanced therapeutic options for the management of PsA in daily clinical practice.

Risankizumab is an approved drug for the treatment of psoriatic arthritis. The study will not be conducted in the United States, however it will be conducted in approximately 15 countries and include at least 900 and up to 1200 participants with a 2 to1 ratio of participant allocation between participants receiving risankizumab and participants receiving other advanced therapeutic agents.

The therapy is prescribed in the usual manner in accordance with the terms of the local marketing authorization and professional and reimbursement guidelines with regards to dose, population, and indication. All study visits will occur during routine clinical practice and participants will be followed for 24 months.

There is expected to be no additional burden for participants in this study.

Inclusion: Participant with a clinical diagnosis of psoriatic arthritis (PsA) with symptom onset at least 6 months prior to the Screening visit and fulfillment of ClASsification for Psoriatic ARthritis (CASPAR) at Baseline visit to confirm that the participant has active disease; Participant must have demonstrated an inadequate response to at least 1 Disease-modifying antirheumatic drug (DMARD) (with max 50% Biologic DMARD-Inadequate Response); alternatively, participant must have demonstrated an intolerance to or contraindication for csDMARDs as determined by the investigator.

Exclusion: Participants demonstrated an inadequate response to three or more bDMARDs/targeted synthetic DMARDs (tsDMARDs).

ClinicalTrials.gov NCT06764693