Release Date: January 31, 2023
Expiration Date: January 31, 2024
Activity Overview
Immunoglobulin (Ig) A nephropathy (IgAN) is the most common form of primary glomerulonephritis worldwide, and it is considered a significant cause of end-stage renal disease (ESRD) in young adults. The precise pathogenesis of IgAN remains unclear. The clinical and pathological features vary significantly between individuals and races, which makes treating IgAN challenging. In most cases, the therapeutic strategies in IgAN are optimal blood pressure control and proteinuria remission to improve the renal functions. Immunosuppressive agents, such as corticosteroids, can be considered in patients with persistent proteinuria and a high risk of renal function decline; however, they include a high toxicity profile.
Various pharmacological therapeutic targets are emerging based on the evolving understanding of the autoimmune pathogenesis of the progression of IgAN, which involves the immune response, mucosal immunity, renal inflammation, complement activation, and autophagy. In this online activity, expert faculty provide information to help health care providers stay up to date on recent findings regarding the pathophysiology of IgAN, and the efficacy and safety profiles of available and emerging agents.
Target Audience
This activity is intended for nephrologists, primary care providers, specialty pharmacists, managed care professionals, nurse practitioners, physician assistants, registered nurses, and other members of the IgAN care team.
Learning Objectives
Upon successful completion of this activity, you should be better prepared to:
- Assess the pathophysiology of the disease progression of IgAN as potential targets for novel therapy
- Summarize recent evidence-based guidelines for the management of IgAN
- Analyze recent efficacy and safety trial data on new and emerging treatment for IgAN
- Design individualized treatment plans for patients with IgAN based on principles of multidisciplinary care

Richard Lafayette, MD, FACP
Professor, Medicine (Nephrology)
Director, Glomerular Disease Center
Stanford University Medical Center
Stanford, CA
Disclosures: Grant/Research Support: Alexion, Appellis, Calliditas, Chinook, Omeros, Otsuka, Pfizer, Travere; Consultant: Alexion, Calliditas, Chinook, GSK, Novartis, Omeros, Otsuka, Pfizer, Travere

Whitney Simmons, APRN-CNP, IgCN
Community Outreach Coordinator and Patient Ambassador for the IgA Nephropathy Foundation
Current Board Member of the IgA Nephropathy Medical and Scientific Advisory Board
Mosaic Infusion Solutions
Oklahoma City, OK
Disclosures: Whitney Simmons, APRN-CNP, IgCN, has no relevant financial relationships with ineligible companies.

Michelle M. Richardson, PharmD, BCPS
Special and Scientific Staff
William B. Schwartz Division of Nephrology
Assistant Professor of Medicine
Tufts University School of Medicine
Boston, MA
Disclosures: Michelle M. Richardson, PharmD, BCPS, has no relevant financial relationships with ineligible companies.
Faculty, Staff, and Planners’ Disclosures
The staff of Physicians’ Education Resource®, LLC, have no relevant financial relationships with ineligible companies.
PER® mitigated all COI for faculty, staff, and planners prior to the start of this activity by using a multistep process.
Off-Label Disclosure and Disclaimer
This activity may or may not discuss investigational, unapproved, or off-label use of drugs. Learners are advised to consult prescribing information for any products discussed. The information provided in this accredited activity is for continuing education purposes only and is not meant to substitute for the independent clinical judgment of a health care professional relative to diagnostic, treatment, or management options for a specific patient’s medical condition. The opinions expressed in the content are solely those of the individual faculty members and do not reflect those of PER® or any company that provided commercial support for this activity.

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