Video

Burst CME: Targeted Therapy for Optimal Psoriasis Management

Release Date

March 31, 2025

Expiration Date

April 1, 2026

Credits

0.5 CME

Release Date: 3/31/2025

Expiration Date: 3/31/2026

Activity Overview

Biologic agents targeting the IL-23/IL-17 axis have demonstrated improved efficacy compared to conventional therapies and include several US Food and Drug Administration (FDA) approved agents for the treatment of PsO: (1) anti-IL-23, ie, tildrakizumab-asmn, guselkumab, and risankizumab-rzaa, (2) anti-IL-12/IL-23, ie, ustekinumab, (3) anti-IL-17A, ie, ixekizumab, secukinumab, and brodalumab, and (4) anti-IL-17A and F, ie, bimekizumab-bkzx.

The purpose of this Burst CME continuing education program is to increase the knowledge of clinicians on the key therapeutic targets within the IL-23/IL-17 pathway and the role of therapeutic monoclonal antibodies directed against these key targets in the management of psoriasis. The mechanisms of action, efficacy, safety, and limitations of these agents will also be discussed by expert faculty Dr Tina Bhutani, as well as identifying patients who would optimally benefit from anti-IL-17 and IL-23 therapies via improvement of long- term outcomes and quality of life.

Target Audience

This educational activity is directed toward dermatologists, internists, NPs, PAs, RNs, and other HCPs involved in the management of psoriasis.

Learning Objectives

Upon successful completion of this activity, you should be better prepared to:

  • Describe the association between the IL-23/TH17 inflammatory pathway and the pathogenesis of PsO
  • Implement prescribing strategies for the incorporation of IL-17 or IL-23 mAbs in the treatment of PsO based on long-term clinical evidence

Course

Burst CME: Targeted Therapy for Optimal Psoriasis Management

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