Evolution of Auto-Substitution in Biosimilar Landscape

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

Now Viewing

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

This is a video synopsis/summary of a panel discussion involving distinguished experts in the medical field: Ryan Haumschild, PharmD, MS, MBA; Alice B. Gottlieb, MD, PhD; Bincy Abraham, MD, MS; Jamie T. Brogan, APRN; and Vibeke Strand, MD. The focus of this segment is on interchangeability studies and automatic substitution.

Haumschild initiates the discussion by emphasizing the importance of understanding interchangeability studies in the context of biosimilars. Haumschild delves into the evolving landscape of biosimilars, stressing the need for robust clinical data to establish interchangeability.

Brogan provides a practical perspective on automatic substitution. She discusses the challenges faced by health care providers, emphasizing the potential impact on patient care. She underscores the importance of transparent communication in navigating the complexities associated with automatic substitution.

Gottlieb contributes insights into the intricacies of interchangeability studies. She highlights the challenges associated with extrapolating data and underscores the need for comprehensive studies to ensure the safety and efficacy of biosimilars.

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