After 8 years of trastuzumab biosimilar competition and slow uptake, a new report shows that trastuzumab biosimilar discounts from the reference product (Herceptin) doubled between 2019 and 2022.
Researchers found that discounts for trastuzumab biosimilars have doubled in the last few years, showing that increased competition on the US market is resulting in lowering prices despite a slow growth for the biosimilar industry.
The report, published by the University of Southern California (USC) Leonard D. Schaeffer Center for Health Policy & Economics in Health Affairs, analyzed pricing trends for Herceptin (reference trastuzumab) and its 5 biosimilar competitors (Kanjinti, Ogivri, Ontruzant, Herzuma, and Trazimera), the first of which launched in July 2019 (Kanjinti) and the last launched in April 2020 (Ontruzant). The study is one of the first to look at multiple biosimilar competitors in terms of US market share, price, and prescribing habits.
Trastuzumab products are used to treat HER2-positive breast, stomach, and gastroesophageal junction cancer. Herceptin was approved by the FDA in September 1998. Since the introduction of biosimilars on the US market, biosimilars have faced several challenges to entering the market and obtaining market share, including patent thickets, delayed entrance dates, lack of education and trust among patients and providers, access issues due to payers not placing them on formularies, and provider prescribing incentives (rebates and reimbursement) prioritizing reference products.
“Trastuzumab is the best example to date of biosimilars fulfilling their promise to reduce biologic drug prices…. In just 3 years, the trastuzumab market displayed important hallmarks of competition: doctors could choose among 6 products; new entrants rapidly captured market share from the originator; and prices steadily declined on all 6 options,” Alice Chen, PhD, coauthor of the study, an associate professor and vice dean for research at the USC Sol Price School of Public Policy, and senior fellow at the USC Schaeffer Center, said in a statement.
By the second quarter of 2022, the average sales prices for trastuzumab biosimilars ranged from 28% to 58% lower than Herceptin’s, a significant increase from the first quarter of 2019, which ranged from 15% to 46% lower than Herceptin’s precompetition net price.
Additionally, the Herceptin’s average sales price fell 21% from $101 to $80 per 10 mg as a result of biosimilar competition.
Kanjinti was found to have the “first-mover advantage” over the other trastuzumab biosimilars by having the highest market share in most states. Hospital-based physicians prescribing trastuzumab tended to prescribe either the reference product or a biosimilar, but not both. However, office-based physicians were more likely to prescribe the reference product and biosimilars more evenly.
“Our analysis applies to a physician-administered drug under Medicare Part B, and provides the best evidence so far that biosimilars can reduce originator drug prices quickly, in the same way that generics reduce prices of small-molecule drugs…. Our findings support the growing body of evidence that biosimilars do in fact reduce biologic drug prices in the physician-administered market. Whether they can do the same in the retail drug market remains to be seen, as the industry brings more of these products to the market,” said coauthor Karen Van Nuys, PhD, executive director of the Value of Life Sciences Innovation program and a senior fellow at the USC Schaeffer Center.
13 Strategies to Avoid the Nocebo Effect During Biosimilar Switching
December 18th 2024A systematic review identified 13 strategies, including patient and provider education, empathetic communication, and shared decision-making, to mitigate the nocebo effect in biosimilar switching, emphasizing the need for a multifaceted approach to improve patient perceptions and therapeutic outcomes.
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.
Review Confirms Clinical Safety of Sandoz Denosumab Biosimilar vs Originator
December 11th 2024Sandoz's biosimilar denosumab (Jubbonti/Wyost) has demonstrated analytical, pharmacokinetic, pharmacodynamic, and clinical equivalence to reference denosumab (Prolia/Xgeva), supporting its approval and extrapolation to all approved indications.
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.
Pertuzumab Biosimilar Shows Promise in HER2-Positive Breast Cancer Treatment
December 9th 2024The proposed pertuzumab biosimilar QL1209 demonstrated equivalent efficacy and safety to reference pertuzumab (Perjeta) in neoadjuvant treatment of HER2-positive, ER/PR-negative early or locally advanced breast cancer, offering a cost-effective alternative with comparable clinical outcomes.
Switching to Rituximab Biosimilars Is Safe, Effective for Patients With Oncohematological Diseases
December 5th 2024Patients with oncohematological diseases switching to rituximab biosimilars experienced similar safety and efficacy, highlighting biosimilars' potential for cost-effective treatment across various medical conditions.