Available Until 2/26/2027

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Changing Therapeutic Landscape and the Role of the Pharmacist

ACPE Number: 0204-0000-25-414-H01-P
Content Release Date: February 26, 2026
Expiration Date: February 26, 2027
Activity Type: Application-based
CE Credits: 1.5 contact hours (0.15 CEUs)
Activity Fee:  Free

Activity Overview

Chronic inflammatory demyelinating polyneuropathy (CIDP) is an immune-mediated, rare disorder leading to muscle weakness and sensory disturbance. It can be debilitating and lead to impaired mobility, difficulty or inability to perform activities of daily living, and severe disability. Conventional therapies are beneficial for patients with CIDP, but there are limitations associated with these therapies requiring consideration of the individual needs of the patient. New and emerging therapies including FcRn antagonists provide targeted therapies, and pharmacists must be aware of the current clinical evidence, appropriate patient selection, identifying where these agents fit within the current treatment algorithm, and methods to transition patients to these therapies to provide individualized, patient-centered care and improve patient outcomes.

This educational activity will discuss the pathophysiology of CIDP as well as the incidence, prevalence, clinical course, and burden of disease. A review of the current guideline-recommended therapies will be discussed, including any treatment limitations. The most recent clinical evidence of new and emerging therapies in CIDP will be explored and opportunities for pharmacists to improve patient care through optimizing therapy, medication monitoring, providing access to medications, patient education, promoting adherence, care coordination, and adjunct care including recommending appropriate vaccinations.

*Please note, this activity was presented live on December 8, 2025 as part of the ASHP 2025 Midyear Clinical Meeting & Exhibition. You can only claim credit once for this activity; live or home study.

Provided by ASHP.

Supported by an independent educational grant from argenx.