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Taking people in GermanyNo phase

Studies how risankizumab affects quality of life in plaque psoriasis

Follows adults with moderate-to-severe plaque psoriasis receiving risankizumab in routine care.

Plain-language title generated from the registry record
Registry title: Study to Assess Change in Quality of Life of Risankizumab Treatment in Adult Participants With Moderate-to-Severe Plaque Psoriasis

Key facts

Where
Dortmund, Friedrichshafen, Hamburg, Heilbad Heiligenstadt, Kulmbach, Leipzig, Mainz, Mölln, Munich, Potsdam, and Schwelm, GermanySee the 12 sites

Where in Germany

  • Klinikum Dortmund Klinikzentrum Mitte /ID# 284856Dortmund, GermanyTaking people
  • Dr. med. Moritz Huber und Dr. med. Martin Heister /ID# 277627Friedrichshafen, GermanyTaking people
  • Cutaneum /ID# 277294Hamburg, GermanyTaking people
  • Universitaetsklinikum Hamburg-Eppendorf /ID# 277164Hamburg, GermanyTaking people
  • Private Practice - Dr. Mario Pawlak /ID# 277465Heilbad Heiligenstadt, GermanyTaking people
  • Dermakulm /Id# 277864Kulmbach, GermanyTaking people
  • Hautarztpraxis Dr. Med. Ulrike Wiemers / Dr. Med. Franca Wiemers /ID# 277821Leipzig, GermanyNo longer taking part
  • Universitaetsmedizin Mainz /ID# 278229Mainz, GermanyTaking people
  • Dermatologie Moelln Praxis Dr. Bodo Segert /ID# 277628Mölln, GermanyTaking people
  • Dermazent /Id# 280327Munich, GermanyTaking people
  • Hautaerzte am Nauener Tor /ID# 284579Potsdam, GermanyTaking people
  • Hautarztpraxis Schwelm /ID# 277464Schwelm, GermanyTaking 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?
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Trial details

Who runs it
AbbVie
Trial code
NCT07039110
Record updated
1 October 2026
Original description
Psoriasis is a chronic, systemic, inflammatory disease in which skin cells build up and develop thick, red and white scaly patches on the skin. This study will assess the change in quality of life of risankizumab treatment in adult participants with moderate to severe plaque psoriasis real-world clinical practice.Read full original descriptionShow less

The Real-World Impact of Risankizumab on the Quality of Life and Cumulative Life Course Impairment (CLCI) in Patients With Moderate-to-Severe Plaque Psoriasis (DREAM)

Psoriasis is a chronic, systemic, inflammatory disease in which skin cells build up and develop thick, red and white scaly patches on the skin. This study will assess the change in quality of life of risankizumab treatment in adult participants with moderate to severe plaque psoriasis real-world clinical practice.

Risankizumab is an approved drug for treating participants with Psoriasis. Approximately 700 participants who are prescribed risankizumab by their physician in accordance with local label will be enrolled in approximately 70 sites worldwide.

Participants will receive risankizumab as prescribed by their physician according to their routine clinical practice and local label. Participants will be followed for up to 2.5 years.

There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.

Inclusion: Participants with a Confirmed diagnosis of moderate-to-severe plaque psoriasis with or without joint involvement according to the treating physician's clinical judgment, prior to time of enrollment; Treatment with risankizumab is indicated per summary of product characteristics (SmPC) or local label and local prescribing/treatment guidelines; Decision to treat with risankizumab is made prior to and independently of study participation.

Exclusion: Currently receiving other biologic treatments and/or small molecules including Janus kinase (JAK) inhibitors, tyrosine kinase 2 (TYK2) inhibitors, and phosphodiesterase 4 (PDE4) inhibitors for any reason; History of a sleep disorder diagnosis which the patient is currently being treated for; Current or recent (within the last 30 days) participation in an interventional clinical trial or an observational study.

ClinicalTrials.gov NCT07039110