During 2019, The Center for Biosimilars® provided interviews and discussions with key opinion leaders on our podcast to discuss various issues affecting biosimilars. From patent issues to the arrival of oncology biosimilars, here is a look at our top 5 podcast episodes from 2019.
During 2019, The Center for Biosimilars® provided interviews and discussions with key opinion leaders on our podcast, “Not So Different,” to discuss various issues affecting biosimilars. From patent issues to the arrival of oncology biosimilars, here is a look at our top 5 podcast episodes from 2019.
5. "What's Holding Back Biosimilars? It May Not Be Pay-for-Delay Deals
Pay-for-delay issues were big news on Capitol Hill, and some experts questioned whether these kinds of settlements are really at the heart of delayed biosimilar competition. Might there be alternative ways to think about, and fix, the problem? On this episode, we spoke with 2 such experts, Imron Aly, JD, and Joel Wallace, JD. Both are partners at Schiff Hardin LLP and have extensive experience with Hatch-Waxman and biosimilars intellectual property issues.
4. A Look Ahead to Biosimilar Insulin
2020 will bring the transition of insulin to regulation as biologics. On this episode, we spoke with one of the experts who testified at a FDA public hearing about biosimilar insulins, which happened amid growing concern about the skyrocketing cost of insulin in the United States. Steven Lucio, PharmD, BCPS, associate vice president of clinical solutions and pharmacy program development at Vizient, shared his thoughts with us on biosimilar insulins, interchangeability, biosimilar suffixes, and what milestones lie ahead as the United States approaches the transition.
3. Is It Time to Give Up on Biosimilars?
It’s no secret that the biosimilars market in the United States has been off to a sluggish start. In fact, former FDA Commissioner Scott Gottlieb, MD, went so far as to call the market anemic. On this episode, we talked with Mark Trusheim, MS, one of the authors of a proposal to do away with the US biosimilars market altogether. Trusheim, a biopharmaceuticals consultant, is also the strategic director of the NEWDIGS program at the Massachusetts Institute of Technology (MIT) Center for Biomedical innovation and a visiting scientist in applied economics at MIT’s Sloan School of Management.
2. Where Are We Headed With Oncology Biosimilars? Vizient Weighs In
In its semiannual drug pricing forecast, healthcare performance company Vizient said that biosimilars will be a key part of combatting rising spending on drugs. We spoke once again with Vizient’s Steven Lucio, PharmD, BCPS, on how oncology biosimilars are poised to make an impact.
1. What Have We Learned So Far About US Oncology Biosimilars?
Among the biggest biosimilars news of this year was the launch of the first 2 anticancer biosimilars. On this episode, we talked with an expert who's sharing her insight into these developments in the oncology space. Christina Corridon, MPH, MBA, is a principal at the professional services firm ZS Associates, where she is a leader in ZS' oncology practice and leads their biosimilars vertical. She joined us to talk about the state of play in the US biosimilars market, what we can learn from ongoing experience, and how sustainable the US market for biosimilars may be today.
A Banner Year for Biosimilars: The 19 FDA Approvals From 2024
January 21st 2025In 2024, the FDA approved 19 biosimilars across various therapeutic areas, including the first biosimilars for ustekinumab and denosumab, marking significant progress in expanding treatment options and market competition.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
FTC Releases Second Report on PBMs Meddling in Generic Drug Markets
January 19th 2025The 3 largest pharmacy benefit managers (PBMs) increased many specialty generic drugs prices by hundreds of percent, with some drugs seeing thousands of percent markups, according to the Federal Trade Commission (FTC)’s second interim report on PBM practices.
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 Drive Cost Savings and Achieve 53% Market Share Across Treatment Areas
January 16th 2025Biosimilar launches achieve a 53% market share and a 53% reduction in average drug costs after 5 years of biosimilar competition, according to Samsung Bioepis’ most recent market report, showcasing notable pricing trends and market share disparities across therapeutic areas.