Initiating Biosimilar Treatment in Patients Without Previous Reference Biologic Experience

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

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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 a multidisciplinary team of experts: Ryan Haumschild, PharmD, MS, MBA; Alice B. Gottlieb, MD, PhD; Bincy Abraham, MD, MS; Jamie T. Brogan, APRN; and Vibeke Strand, MD. In this segment, the focus shifts to the initiation of biosimilars, particularly for patients who have never been prescribed the originator biologic.

Haumschild begins the conversation by underscoring the significance of the patient perspective in initiating biosimilars. He emphasizes the role of shared decision-making in this context, acknowledging that discussions might differ when initiating someone who has never received the reference biologic compared with someone who has experience with it.

Strand, an authoritative voice in rheumatology, offers insights into best practices for initiating biosimilars in patients unfamiliar with the reference biologic. She emphasizes the importance of shared decision-making and anticipates scenarios where providers may need to make informed decisions on behalf of patients. Strand highlights the critical role of explaining biosimilars comprehensively to mitigate the nocebo effect, emphasizing the need for patient education.

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