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Novel Therapeutics in Psoriatic Arthritis. What Is in the Pipeline?

  • Psoriatic Arthritis (J Scher, Section Editor)
  • Published:
Current Rheumatology Reports Aims and scope Submit manuscript

Abstract

Purpose of Review

To highlight the recently approved therapeutic agents in psoriatic arthritis (PsA), drugs in the pipeline, as well as to discuss efficacy with regard to different clinical domains of PsA.

Recent Findings

More than 15 years ago, tumor necrosis factor inhibitors (TNFi) were the first biologic disease modifying anti-rheumatic drugs (bDMARDs) that were approved for the treatment of PsA. Since then, multiple new therapeutic agents inhibiting other targets have emerged including biologics targeting interleukin (IL) 12/23, and IL 17 and oral agents targeting phosphodiesterase 4 (PDE4) and Janus kinases (JAKs). Many new agents with various modes of action including selective inhibition of IL 23, therapies promoting activated T cell apoptosis, inhibition of tyrosine kinase 2 (TYK2), and more are under active assessment in ongoing clinical trials.

Summary

Effective therapies for treating PsA have emerged over the last 15 years and newer agents continue to be discovered, allowing greater therapeutic options for controlling psoriatic disease activity and preventing joint damage and disability. Personalized therapy for patients with PsA is now a possibility.

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Correspondence to Vinod Chandran.

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Dr. Elalouf declares no conflict of interest.

Dr. Chandran reports personal fees from Amgen, grants and personal fees from Abbvie, grants and personal fees from Celgene, personal fees from Eli Lilly, personal fees from Janssen, personal fees from Novartis, personal fees from UCB, and personal fees from Pfizer, during the conduct of the study.

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This article does not contain any studies with human or animal subjects performed by any of the authors.

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This article is part of Topical Collection on Psoriatic Arthritis

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Elalouf, O., Chandran, V. Novel Therapeutics in Psoriatic Arthritis. What Is in the Pipeline?. Curr Rheumatol Rep 20, 36 (2018). https://doi.org/10.1007/s11926-018-0746-0

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