The use of bevacizumab products for ophthalmic conditions will continue to evolve as the market grows. However, off-label usage will likely be the norm, according to Sonia T. Oskouei, PharmD, BCMAS, DPLA, vice president of biosimilars at Cardinal Health, at Asembia’s Specialty Pharmacy Summit.
The use of bevacizumab products for ophthalmic conditions will continue to evolve as the market grows. However, off-label usage will likely be the norm, according to Sonia T. Oskouei, PharmD, BCMAS, DPLA, vice president of biosimilars at Cardinal Health, at Asembia’s Specialty Pharmacy Summit.
Transcript
Do you think that the potential for more bevacizumab biosimilars coupled with the recent approval of Alymsys will encourage more companies to seek indication expansions for ophthalmic conditions?
Oskouei: The role of bevacizumab in ophthalmology use is likely to continue to evolve. So, today you have off-label Avastin [reference bevacizumab] being used as one of the most common anti-VEGF [vascular endothelial growth factor] treatment options for retina conditions. However, we now have Avastin or bevacizumab biosimilars, but these are primarily being used in oncology indications. But the reason why this is going to continue to evolve is you also have Outlook Therapeutics with a bevacizumab candidate [Lytenava; ONS-5010; bevacizumab-vikg] that is seeking on-label indication for ophthalmology use.
So, these dynamics are going to shift the types of use for the product and the treatment plan when evaluating treatment options for retina conditions. But not only do you have the bevacizumab scenario and dynamics going on, you also have increasing market entrance of additional innovative treatment options for ophthalmology. And I really believe these past couple years and a couple of years moving forward is a very innovative time period for ophthalmology treatment options. We have new treatment options, from port delivery systems to novel mechanisms of actions, coming into market and competing both with originator biologics and biosimilars.
So, I don't particularly foresee that bevacizumab biosimilars are going to start competing or seeking additional indications in ophthalmology, especially because the originator product does not have it as an on-label indication. However, I think the use of the product is going to continue to evolve as these market dynamics evolve.
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 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.
Improving Biosimilar Access Through Global Regulatory Convergence
January 15th 2025Achieving global regulatory harmonization for biosimilar vaccines and immunotherapies is essential to improving market access, reducing costs, and enhancing patient outcomes by streamlining approval processes, fostering international collaboration, and addressing regulatory disparities.
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.
Eye on Pharma: Korean Drugmakers’ Impact in Europe; New Denosumab, Eculizumab Deals
January 11th 2025Korean drugmakers hold over 50% market share in the 6 best-selling biosimilar markets, 2 companies sign exclusive licensing partnership for a denosumab biosimilar, and 2 others join forces for an eculizumab biosimilar.