4.5 Review

Current investigational drugs in psoriasis

期刊

EXPERT OPINION ON INVESTIGATIONAL DRUGS
卷 21, 期 4, 页码 473-487

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1517/13543784.2012.669372

关键词

biologic therapies; interleukin-12; interleukin-17; interleukin-23; janus kinase inhibitors; psoriasis; psoriatic arthritis; secukinumab; Th17 cells

资金

  1. Abbot
  2. Allergan
  3. Amgen
  4. Astellas
  5. Asubio
  6. Celgene
  7. Centocor
  8. DUSA
  9. Eli Lily
  10. Genentech
  11. Novartis
  12. Novo Nordisk
  13. Pfizer
  14. Promius
  15. Stietel
  16. Synthrix Biosystems
  17. Galderma
  18. Merck-Serono
  19. Stiefel
  20. Syntrix Biosystems
  21. Warner Chilcott

向作者/读者索取更多资源

Introduction: The advent of biologic therapies has revolutionized the treatment of psoriasis. Increased understanding of immunogenetic pathways has allowed for the development of more selective targeted biologic therapies. Multiple new treatments are currently in development for the treatment of psoriasis. Preliminary data for many of these agents, particularly with regard to agents targeting the IL-23/Th17 pathway, are promising. Proven long-term safety, however, is an absolute necessity with newly developed drugs, and should, therefore, still be considered second-line agents to current established treatments with long-term safety data. Areas covered: This review details the mechanisms of action of drugs currently in development or in clinical trials for the treatment of psoriasis, using clinical trial registries and associated publications. Readers will gain a comprehensive overview about the mechanism of action of emerging treatments targeting various immune pathways deeply involved in psoriasis. Pathogenesis, clinical efficacy and safety data for these treatments are discussed where available. Expert opinion: Psoriasis remains a heavily undertreated systemic immune-mediated disease despite increased understanding of immunopathogenesis of the disease and advent of a multitude of novel therapeutic agents with potentially improved bioavailability and safety profiles. Limitations, however, remain in the realm of topical agents for treatment of mild to moderate psoriasis, which has seen little progress over the years. A concerted effort will need to be made among researchers, clinicians and patient advocacy groups to ensure new therapeutic agents are developed and gain proper exposure.

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