The new report reviewed the potential impact of biosimilars across multiple specialties.
While 2022 might have been a turning point for biosimilars, 2023 is expected to bring more disruption, according to a new report from Cardinal Health. The 2023 Biosimilars Report1 reviewed the potential impact biosimilars will have in rheumatology, gastroenterology, dermatology, and ophthalmology, and analyzed data on biosimilar utilization, government pricing reform, and payer coverage.
The report surveyed 350 providers and provided an analysis of how the market may be affected with as many as 10 adalimumab biosimilars launching in 2023. Currently, there are 8 FDA-approved adalimumab biosimilars. The first, Amjevita, has already launched and will have market exclusivity for 6 months.
Although biosimilars may have had a slow start in the United States, they have become an important tool to drive substantial cost savings for some of the most expensive biologics on the market, Bruce Feinberg, DO, vice president and chief medical officer, Cardinal Health, wrote in the report.
"Biosimilars bring competition and lower costs to patient-critical treatments," he said in a statement.2 "In order to deliver on the promise of these drugs from a health equity standpoint, we must continue to analyze prescriber awareness and familiarity. Through our research, Cardinal Health seeks to understand prescribers' perceptions and what other factors are moving the industry forward—from business and financial decisions to provider adoption."
The report noted a growing familiarity of biosimilars among rheumatologists, with 76% now saying they are very familiar with these products compared with 56% in a report released June 2022. Only gastroenterologists reported being more familiar, with 81% saying they were very familiar with biosimilars. Ophthalmologists and dermatologists were much farther behind, with only 33% and 31%, respectively, saying they were very familiar.
Gastroenterologists reported that they needed the smallest discount on price to be motivated to switch to a biosimilar. Forty percent said they only needed a discount of 30% or less from the reference product, while 36% of ophthalmologists said they needed a discount greater than 40%. However, dermatologists were the most likely (20%) to say no discount would motivate them to prescribe the biosimilar over a reference product.
The first ranibizumab biosimilar in ophthalmology launched July 2022 at a 40% discount to the reference product. More than half (58%) said the 40% discount made them more likely to prescribe the biosimilar Byooviz over the reference product Lucentis. However, 31% said the discount had no impact and 11% said it made them less likely to prescribe the biosimilar. A second ranibizumab biosimilar launched in October 2022 with the interchangeability designation.
“While it is still too early to tell as of this writing how the early launches have fared from an adoption standpoint, we expect share shifts in the ophthalmology market to evolve more slowly as our market research data reveals significant provider hesitation with biosimilars remains,” the Cardinal Health report noted.
When it came to prescribing decisions:
All dermatologists, rheumatologists, and gastroenterologists were asked about adalimumab biosimilars. By specialty, the top concerns regarding adalimumab were:
All specialties cited clinical and/or real-world evidence studies as key decision criteria for utilizing an adalimumab biosimilar. Real-world evidence, either gathered internationally or domestically, was cited as the best way to support clinical confidence to utilize adalimumab biosimilars in both new and existing patients eligible for adalimumab.
“These findings further highlight the continued need for education to strengthen clinical confidence in these agents and help overcome key barriers to a more robust biosimilars market in the US,” according to the report.
This article originally appeared on AJMC.