Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
3500 participants
OBSERVATIONAL
2008-01-31
2032-12-31
Brief Summary
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Detailed Description
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Objectives: Observation and analysis of the following outcomes of treatment with systemic antipsoriatics:
1. Effectiveness in clinical practice ("real world")
2. Benefits and needs on the patients' side
3. Effectiveness in a long-term course over years
4. Optimal maintenance dosages
5. Safety and side-effects profile under routine conditions
6. Use in case of and effect on co-morbidity
7. Reliable predictors of response
8. Benefit and effectiveness of possible combination therapies or alternating use of biologics and systemic therapies
Methods: The registry evaluates the long-term course of 3,500 patients with Pso and PsA treated with systemic antipsoriatics.The registry started for seven treatment arms: Fumaric acid, methotrexate, ciclosporin A, efalizumab, etanercept, infliximab and adalimumab. While efalizumab was withdrawn from the market, ustekinumab was included after authorization. Patients are included at first initiation of a given treatment and will remain in the registry for 5 years, regardless of subsequent therapy. Nationwide, dermatologic practices and hospital ambulances with expertise in systemic and biologic treatment consecutively enrol patients. Follow-ups will be every 3 to 6 months, comprising patient and treatment characteristics, clinical parameters, patient-defined benefit, quality of life and adverse events. Standardized questionnaires will be addressed to the patient and to the dermatologist 12 times at the dermatologic centres. In interim intervals, patients are directly contacted another 9 times by mail. PsoBest is member of the ENCePP network of psoriasis-registries (www.psonet.eu).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Fumaric acid esters
Intervention: Drug: conventional systemic: Fumaric acid esters, including Dimethylfumarate, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Methotrexate
Intervention: Drug: conventional systemic: Methotrexate, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Cyclosporine A
Intervention: Drug: conventional systemic: Cyclosporine A, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Efalizumab (withdrawn)
Intervention: Biological: Efalizumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Etanercept
Intervention: Biological and biosimilars: Etanercept, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Infliximab
Intervention: Biological and Biosimilars/-identicals: Infliximab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Adalimumab
Intervention: Biological and Biosimilars: Adalimumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Ustekinumab
Intervention: Biological and Biosimilars: Ustekinumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Golimumab
Intervention: Biological: Golimumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Secukinumab
Intervention: Biological: Secukinumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Apremilast
Intervention: Small molecule: Apremilast, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Certolizumab
Intervention: Biological: Certolizumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Retinoids
Intervention: Drug: conventional systemic: Retinoids, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Leflunomids
Intervention: Drug: conventional systemic: Leflunomids, all dosages, frequencies and durations prescribed
No interventions assigned to this group
systemic PUVA
Intervention: Drug: conventional systemic: systemic PUVA, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Guselkumab
Intervention: Biological: Guselkumab all dosages, frequencies and durations prescribed
No interventions assigned to this group
Brodalumab
Intervention: Biological: Brodalumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Tildrakizumab
Intervention: Biological: Tildrakizumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Risankizumab
Intervention: Biological: systemic Risankizumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Bimekizumab
Intervention: Biological: Bimekizumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Tofacitinib
Intervention: JAK-Inhibitor: Tofacitinib, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Upadacitinib
Intervention: JAK-Inhibitor: Upadacitinib, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Deucravacitinib
Intervention: JAK-Inhibitor: Deucravacitinib, all dosages, frequencies and durations prescribed
No interventions assigned to this group
Ixekizumab
Intervention: Biological: Ixekizumab, all dosages, frequencies and durations prescribed
No interventions assigned to this group
No treatment
Intervention: no systemic treatment in observation episodes
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* age ≥ 18 years
* being administered a specific systemic drug for the first time
* informed consent to participate
* sufficient language skills (German)
Exclusion Criteria
* patients being participants of clinical trials at the day of admission to the registry (if a patient is included into a clinical trial during the registry follow-ups, the patient data will be recorded, but analysed separately)
18 Years
ALL
No
Sponsors
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Berufsverband der Deutschen Dermatologen e.V. (www.bvdd.de)
UNKNOWN
Deutsche Dermatologische Gesellschaft e.V. (https://derma.de)
UNKNOWN
AbbVie
INDUSTRY
Biogen
INDUSTRY
Janssen-Cilag G.m.b.H
INDUSTRY
medac GmbH
INDUSTRY
Merck Sharp & Dohme LLC
INDUSTRY
Novartis Pharmaceuticals
INDUSTRY
Pfizer Pharmaceuticals Ltd.
INDUSTRY
Merck Serono GmbH, Germany
INDUSTRY
PsoNet.eu (http://www.psonet.eu/)
UNKNOWN
Celgene
INDUSTRY
Eli Lilly and Company
INDUSTRY
Amgen
INDUSTRY
Almirall Hermal GmbH
INDUSTRY
UCB Pharma
INDUSTRY
Bristol-Myers Squibb
INDUSTRY
Viatris Inc.
INDUSTRY
LEO Pharma
INDUSTRY
Universitätsklinikum Hamburg-Eppendorf
OTHER
Responsible Party
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Principal Investigators
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Matthias Augustin, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
Universitätsklinikum Hamburg-Eppendorf
Locations
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Nationwide group of dermatological centers, hospitals and medical offices
Hamburg, , Germany
Countries
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Facility Contacts
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Related Links
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PsoBest - the German psoriasis registry
German Center for Health Services Research in Dermatology
PsoNet - the European registry of psoriasis
Swiss Dermatology Network for Targeted Therapies (SDNTT)
Other Identifiers
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IVDP-085-07
Identifier Type: -
Identifier Source: org_study_id
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