Utilizing Recently Approved Biosimilars in Clinical Practice

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EP: 1.Utilizing Recently Approved Biosimilars in Clinical Practice

EP: 2.Transitioning to Biosimilars: Considerations for Providers and Payers

EP: 3.Navigating Challenges Associated with Biosimilars Across Various Disease States

EP: 4.Provider Acceptance Driving Confidence in Biosimilar Therapy

EP: 5.Decision-Making Process Surrounding Biosimilar Implementation

EP: 6.Biosimilar Administration Considerations Impacting Patient Experience

EP: 7.Initiating Biosimilar Treatment in Patients Without Previous Reference Biologic Experience

EP: 8.Switching Patients from Reference Product to Biosimilar

EP: 9.Defining Interchangeability and Switching in Biologics

EP: 10.Evolution of Auto-Substitution in Biosimilar Landscape

EP: 11.An Overview of Biosimilar Extrapolation During FDA Approval

EP: 12.Harnessing Indication-Specific Data on Biosimilars

EP: 13.Cost Savings Related to Biosimilars

EP: 14.Payers and PBMs Impacted by Biosimilar Integration

EP: 15.Payer Support Driving Lowering of Biosimilar-Related Health Care Costs

EP: 16.Patient Conversations: Managing Patient Expectations Regarding Biosimilars

EP: 17.Key Points of Emphasis Regarding Biosimilar Integration

This is a video synopsis/summary of a panel discussion involving Ryan Haumschild, PharmD, MS, MBA, director of pharmacy services at Emory Healthcare and the Winship Cancer Institute; Alice B. Gottlieb, MD, PhD, clinical professor and medical director in the Department of Dermatology at the Icahn School of Medicine at Mount Sinai; Bincy Abraham, MD, MS, professor of clinical medicine in the Academic Division of Gastroenterology and Hepatology at Houston Methodist Hospital; Jamie T. Brogan, APRN, nurse practitioner at Northwestern Medicine; and Vibeke Strand, MD, biopharmaceutical consultant and adjunct clinical professor in the Division of Immunology and Rheumatology at Stanford University School of Medicine.

The discussion focuses on the evolving landscape of biosimilars, specifically the role of adalimumab biosimilars, in dermatology, gastroenterology, and rheumatology. Gottlieb highlights the exclusive use of infliximab and rituximab biosimilars in her dermatology practice, expressing interest in upcoming adalimumab biosimilars and emphasizing the importance of interchangeability. Abraham, in gastroenterology, stresses the significance of maintaining stability for patients on adalimumab due to the potential consequences of disease flares. Strand, in rheumatology, anticipates the use of adalimumab biosimilars, emphasizing the preference for those with interchangeable designations and citing reassuring data on immunogenicity.

The panel discusses the impact of biosimilars on patient stability, with Haumschild underscoring the importance of avoiding complications or disease progression. The conversation covers the challenges of payer coverage decisions and potential switches to biosimilars. Brogan contributes insights into the auto substitution process, highlighting the need for shared decision-making and patient education.

Video synopsis is AI-generated and reviewed by AJMC editorial staff.