The top 5 most-listened podcast episodes of 2023 covered a range of topics including the US market introduction of adalimumab biosimilars, current market trends, the role of providers in boosting adoption rates, and more.
The top 5 most-listened Not So Different podcast episodes of 2023 covered a range of topics including the US market introduction of adalimumab biosimilars, current market trends, the role of providers in boosting adoption rates, and more.
Here are the most-listened podcasts of 2023.
5. How Community Oncologists Can Break Down Biosimilar Adoption Barriers
Despite the oncology space experiencing successful biosimilar uptake, challenges persist, including pharmacy benefit manager and payer formulary decisions, incentives favoring reference products, and high drug prices. In this episode, Mark Guyot, senior director of unity provider engagement at McKesson, discussed best practices for biosimilar implementation in community oncology practices. Drawing from his work on a real-world analysis at McKesson, he highlighted the impact of successful biosimilar adoption, leading to decreased care costs for patients and annual savings to Medicare exceeding $164 million, emphasizing the unique opportunity for community oncology practices to drive biosimilar adoption and patient savings.
4. Adalimumab Biosimilars Take Center Stage: A Game Changer for IBD Treatment
In July 2023, the US biosimilar industry witnessed a significant moment with the launch of 8 adalimumab biosimilars, making it the month with the highest number of biosimilar options and establishing adalimumab as the drug class with the most alternatives. These biosimilars, referencing Humira, a widely used drug with 11 indications, offer substantial savings, particularly for patients with inflammatory bowel disease (IBD). In this episode, Laura Wingate, executive vice president at the Crohn's & Colitis Foundation, discussed the transformative impact on the gastrointestinal space, emphasizing the need for education resources to address misconceptions and enhance awareness among patients and providers.
3. Pipelines and Preparation: How the US Can Prepare for More RA Biosimilars
In 2023, the United States witnessed the introduction of biosimilars referencing Humira (adalimumab) and Stelara (ustekinumab). Despite the abundance of choices, challenges in storage, education, and payer adoption emerged. In this episode, Robert Zutaut, RPh, Clinical Specialist with McKesson Provider Solutions, explored actions clinicians could take to prepare for the influx of RA biosimilars, emphasizing the need for readiness amid market changes.
2. On the Come Up: What Vizient’s Report Says About Inflation and Biosimilars
Vizient's Winter 2023 Pharmacy Market Outlook Report explored biosimilar market trends, discussing the impact of inflation and the COVID-19 pandemic on biosimilar utilization and overall drug prices. The report anticipated the launch of over 8 biosimilars referencing Humira in the US in 2023 and addressed how payer preferences and white bagging policies may influence their adoption. Carina Dolan, senior director for clinical oncology and pharmaceutical outcomes at Vizient, shared insights on these topics in a podcast episode, drawing from her background as a clinical pharmacist and discussing opportunities and challenges for oncology biosimilars.
1. What AmerisourceBergen's Report Reveals About Payers, Biosimilar Pricing Trends
At Asembia 2023, Tasmina Hydery, associate director of digital solutions at AmerisourceBergen, discussed the future of the biosimilars industry and payer responses to new biosimilar products in the United States. She shared insights from AmerisourceBergen's report, focusing on how payers incorporate biosimilars into formularies, their perspectives on interchangeability, and their use of prior authorization and step therapy strategies to promote preferred products. In the present episode, Hydery, joined by Brian Biehn, senior director of biosimilar commercialization at AmerisourceBergen, further explored these topics and discussed pricing trends in the biosimilars space.
Can Global Policies to Boost Biosimilar Adoption Work in the US?
November 17th 2024On this special episode of Not So Different honoring Global Biosimilars Week, Craig Burton, executive director of the Biosimilars Council, explores how global policies—from incentives to health equity strategies—could boost biosimilar adoption in the US.
Biosimilars Development Roundup for October 2024—Podcast Edition
November 3rd 2024On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, artificial intelligence (AI), and collaboration to enhance the global supply chain for biosimilars and generic drugs, as well as the evolving requirements for biosimilar devices.
Biosimilars Policy Roundup for March 2023—Podcast Edition
April 2nd 2023On this episode of Not So Different, we discuss some of the global biosimilar policy news that came out during the month of March, including a new bill in Congress and 2 Canadian jurisdictions implementing switching policies.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
AAM's Craig Burton: Is the Biden Administration Doing Enough to Help Biosimilars?
November 13th 2022Craig Burton, senior vice president of policy and strategic alliances at the Association for Accessible Medicines and executive director of the Biosimilars Council, gives insight into the many health policies that the Biden administration has implemented in 2022 as well as their possible impact on biosimilar adoption.