PsoBest - The German Psoriasis Registry

NCT ID: NCT01848028

Last Updated: 2025-01-27

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

3500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-01-31

Study Completion Date

2032-12-31

Brief Summary

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Treatment of moderate to severe Psoriasis (Pso) and Psoriasis-Arthritis (PsA) is largely confined to systemic therapy in Germany. Systemic therapy includes conventional systemic therapy (e.g. fumaric acids, methotrexate, ciclosporin A) and biological treatment (e.g. adalimumab, etanercept). While short- and middle-term efficacy of most systemic treatments has been shown in clinical studies (and is incorporated in international guidelines), knowledge about long-term outcomes, optimal treatment and effectiveness under real-world conditions is still missing. PsoBest, the German registry on the treatment of moderate to severe Pso and PsA started in 2008 and documents the long-term course of patients being administered any biologic or conventional systemic antipsoriatic drug authorized in Germany for the first time. The registry evaluates the long-term course of 3,500 patients with Pso and PsA treated with systemic antipsoriatics.

Detailed Description

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Background: Treatment of moderate to severe Psoriasis (Pso) and Psoriasis-Arthritis (PsA) is largely confined to systemic therapy in Germany. Systemic therapy includes conventional systemic therapy (e.g. fumaric acids, methotrexate, ciclosporin A) and biological treatment (e.g. adalimumab, etanercept). While short- and middle-term efficacy of most systemic treatments has been shown in clinical studies (and is incorporated in international guidelines), knowledge about long-term outcomes, optimal treatment and effectiveness under real-world conditions is still missing. PsoBest, the German registry on the treatment of moderate to severe Pso and PsA started in 2008 and documents the long-term course of patients being administered any biologic or conventional systemic antipsoriatic drug authorized in Germany for the first time.

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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Psoriasis Psoriatic-arthritis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

* patients with diagnosis of plaque-type psoriasis or psoriasis arthritis confirmed by a dermatologist
* age ≥ 18 years
* being administered a specific systemic drug for the first time
* informed consent to participate
* sufficient language skills (German)

Exclusion Criteria

* lack of informed consent
* 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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Berufsverband der Deutschen Dermatologen e.V. (www.bvdd.de)

UNKNOWN

Sponsor Role collaborator

Deutsche Dermatologische Gesellschaft e.V. (https://derma.de)

UNKNOWN

Sponsor Role collaborator

AbbVie

INDUSTRY

Sponsor Role collaborator

Biogen

INDUSTRY

Sponsor Role collaborator

Janssen-Cilag G.m.b.H

INDUSTRY

Sponsor Role collaborator

medac GmbH

INDUSTRY

Sponsor Role collaborator

Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role collaborator

Novartis Pharmaceuticals

INDUSTRY

Sponsor Role collaborator

Pfizer Pharmaceuticals Ltd.

INDUSTRY

Sponsor Role collaborator

Merck Serono GmbH, Germany

INDUSTRY

Sponsor Role collaborator

PsoNet.eu (http://www.psonet.eu/)

UNKNOWN

Sponsor Role collaborator

Celgene

INDUSTRY

Sponsor Role collaborator

Eli Lilly and Company

INDUSTRY

Sponsor Role collaborator

Amgen

INDUSTRY

Sponsor Role collaborator

Almirall Hermal GmbH

INDUSTRY

Sponsor Role collaborator

UCB Pharma

INDUSTRY

Sponsor Role collaborator

Bristol-Myers Squibb

INDUSTRY

Sponsor Role collaborator

Viatris Inc.

INDUSTRY

Sponsor Role collaborator

LEO Pharma

INDUSTRY

Sponsor Role collaborator

Universitätsklinikum Hamburg-Eppendorf

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status RECRUITING

Countries

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Germany

Facility Contacts

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Matthias Augustin, Prof. Dr.

Role: primary

Related Links

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https://www.psobest.de/

PsoBest - the German psoriasis registry

https://catalogues.ema.europa.eu/network/25161

PsoNet - the European registry of psoriasis

https://www.sdntt.ch/de/

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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