Bruce A. Feinberg, DO: You introduced cost. Do you really believe it will be a fraction of the cost? It raises the other issue, and you can all weigh in on this. What does that differential need to be? Is a delta of 10% going to be enough to really change behavior? Would it be enough for even a payer to really champion that cause? Does it need to be 30% in order to do that?
Do we have any examples that already exist? The one I can think of is in hepatitis C, but it really took one of the competitors to drop prices by 50% to change the market pattern. I’m curious as to what you think that may be and, in terms of how close that delta might be, how that won’t allow change or how wide it has to be to drive that change?
Hope S. Rugo, MD: From my perspective, the delta has to be at least 20% or more. That’s what people in the general field think. Being an academic oncologist, we really don’t think too much about cost, but we need to be thinking more and more about it. And I think that there is something unique about the supportive care products. You were talking about long-acting agents for rheumatologic diseases, but we don’t really have that in the therapeutic area of oncology. It’s just in supportive care.
You have a combination of what the cost is for the originator product versus the biosimilar in the short-acting area versus giving a long-acting drug, which already costs a lot more than the originator product, versus the 5 doses of filgrastim. So, it’s a complex basis, and sometimes I’ve had insurers come to me and say, “We’re not going to give you growth factor for this patient’s chemotherapy.” And I say, “Well, I can’t give them chemotherapy without growth factor,” and, “Look, here’s the papers that show the rate of febrile neutropenia.” We are really getting into an area where there is a lot of consideration about what people are going to approve up front. We have a lot of peer to peer discussions, now, with insurance companies about what’s going to get approved or not. It’s going to be very interesting to see.
Bruce A. Feinberg, DO: I’m curious. I’m hearing you talk about some of the kind of practical pragmatic issues of everyday patient care, and you’re at a renowned institution. And I’m thinking, when you talk to people in the community, are they suspect? You’re having those kinds of problems. You don’t know what problems are until you’re in a community practice with 3 doctors and you’re trying to deal with an insurance company. And so, I’m surprised by the fact that I’m hearing that recognition coming from your level—that higher position in the hierarchy of medicine in a major institution.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
Biosimilars Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
Breaking Down Biosimilar Barriers: Payer and PBM Policies
November 13th 2024Part 2 of this series for Global Biosimilars Week dives into the complexities of payer and pharmacy benefit manager (PBM) policies, how they impact biosimilar accessibility, and how addressing these issues may look under a second Trump term.
Challenges, Obstacles, and Future Directions for Anti-TNF Biosimilars in IBD
November 9th 2024A review article on tumor necrosis factor (TNF)-α inhibitors in inflammatory bowel disease (IBD) outlined current use of anti-TNF originators and biosimilars, their efficacy and safety, the benefits and challenges of biosimilars, and the future of biosimilars in IBD.