Sonia T. Oskouei, PharmD, vice president of innovation and solution development at Premier Inc, discusses how biosimilars have impacted innovation in oncology.
Transcript
So biosimilars really have had a significant impact at innovation in general, including oncology. And so here's my perspective: I think it not only represents innovation but it also fosters innovation.
So biosimilars, the regulatory pathway, the Biologics Price Competition and Innovation Act, innovation’s in the name, was really innovative to create an expedited pathway to bring these life-saving biologic therapies to market sooner. So not only was the regulatory pathway innovative with creating the concept of extrapolation and relying on the totality of evidence to be able to do so, but also the manufacturing process for these biosimilars represent innovation.
The technology and the ability to develop these biologics have come a long way even since the originator biologics were First developed. Now the way that biosimilars have fostered innovation and continue to do so, we could see it even from the originator biologics, we could see enhanced formulations or even dosage form. So, biologics that were traditionally infused are now available [subcutaneously] to other areas that we see it fostering innovation is even in the health system setting.
Creating these biosimilar strategies and processes from a health system perspective has really catapulted the development of a true education program within health systems to ease the transition to a biosimilar or start a new biosimilar for a new patient. A lot of time that's that goes with educating nurses, physicians, pharmacists, really a multi-stakeholder approach, and really keeping the pressure patient at the forefront of it.
Being able to create the process where patients are notified, educated on what these products are, why it's okay to be switching, and the potential impact it could have on out-of-pocket costs and the finance is really important, and that's represented innovation from a process standpoint within health systems too.
Achieving PFS in Advanced Gastric Cancer With HLX02 Biosimilar, Chemotherapy
November 23rd 2024In a phase 2 study, the addition of HLX22, an anti-HER2 antibody, to HLX02 biosimilar and XELOX (oxaliplatin and capecitabine) chemotherapy extended progression-free survival (PFS) in untreated HER2-positive advanced gastric cancer patients.
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.
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 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.
Samsung Bioepis Report Showcases Adalimumab Biosimilar Growth in Market Share
October 11th 2024Adalimumab biosimilars have seen a significant increase in market share, from 2% in early 2024 to 22%, as payers and pharmacy benefit managers begin to prioritize these biosimilars over the reference product, Humira.
Duke Publishes Recommendations for Developing CGT Biosimilars
October 9th 2024Transformative cell and gene therapies (CGT) offer promising treatments for serious conditions, but high costs and complex biologics limit competition, requiring policies that support the development of biosimilars to enhance affordability and patient access.