PsoBest - The German Psoriasis Registry

NCT01848028 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3500

Last updated 2025-01-27

No results posted yet for this study

Summary

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.

Conditions

Sponsors & Collaborators

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

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

    collaborator UNKNOWN
  • AbbVie

    collaborator INDUSTRY
  • Biogen

    collaborator INDUSTRY
  • Janssen-Cilag G.m.b.H

    collaborator INDUSTRY
  • medac GmbH

    collaborator INDUSTRY
  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • Novartis Pharmaceuticals

    collaborator INDUSTRY
  • Pfizer Pharmaceuticals Ltd.

    collaborator INDUSTRY
  • Merck Serono GmbH, Germany

    collaborator INDUSTRY
  • PsoNet.eu (http://www.psonet.eu/)

    collaborator UNKNOWN
  • Celgene

    collaborator INDUSTRY
  • Eli Lilly and Company

    collaborator INDUSTRY
  • Amgen

    collaborator INDUSTRY
  • Almirall Hermal GmbH

    collaborator INDUSTRY
  • UCB Pharma

    collaborator INDUSTRY
  • Bristol-Myers Squibb

    collaborator INDUSTRY
  • Viatris Inc.

    collaborator INDUSTRY
  • LEO Pharma

    collaborator INDUSTRY
  • Universitätsklinikum Hamburg-Eppendorf

    lead OTHER

Principal Investigators

  • Matthias Augustin, Prof. Dr. · Universitätsklinikum Hamburg-Eppendorf

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2032-12-31
Completion
2032-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01848028 on ClinicalTrials.gov