Chad Pettit, MBA, executive director of Marketing and the Global Biosimilars commercial lead for Amgen, discussed the company’s 2021 Biosimilar Trends Report and his projections for the future of the biosimilars market.
In an interview with The Center forBiosimilars®, Chad Pettit, MBA, executive director of Marketing and Global Biosimilars commercial lead for Amgen, discussed the company’s upcoming 2021 Biosimilar Trends Report, which will be released in September 2021. He also talked about the outlook for the biosimilar industry.
Earlier this summer, a preview of the report was released with observations on biosimilar market share and pricing trends at the wholesale and provider levels.
Looking at the infliximab marketplace, Pettit said the slow uptake of infliximab biosimilars is not a reflection on the health of the biosimilar industry. He expects that interest in biosimilars will increase as more reference products start facing biosimilar competition and more savings are achieved.
Pettit also explained that despite fewer biosimilar approvals in 2020 and 2021, compared with earlier years, the number of biosimilar development programs the FDA is working with has increased, suggesting that a new wave of biosimilar approvals and savings can be expected in the near future.
When asked about current discounts for biosimilars, relative to the cost of reference products, Pettit said price discounts for US biosimilars average 10% to 15% and are significant. He added that cost savings will grow as more competition leads to lower prices for both reference products and biosimilars.
However, Amgen’s July 2020 launch of Avsola (infliximab) on the US market at a 57% discount from the reference product (Remicade) raises the question whether competition is sustainable. It costs money to produce biosimilars and if prices drop too far, too fast, that could discourage manufacturers.
Pettit said that competition should be on a level playing field to ensure that manufacturers are able to invest and the industry is successful.
Although the COVID-19 pandemic diverted the FDA’s attention from biosimilars in 2020, and the number of approvals declined, Pettit is optimistic that this trend will reverse, especially as more competition emerges. He also highlighted pricing trends between different types of biosimilars.
In conclusion, Pettit said the upcoming Amgen report will show that biosimilar uptake and savings data are positive and encouraging. He said that biosimilars will be instrumental in creating sustainability for the biologics market and helping to offset the massive costs often associated with disease burden.
Biosimilars Development Roundup for October 2024—Podcast Edition
November 3rd 2024On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, artificial intelligence (AI), and collaboration to enhance the global supply chain for biosimilars and generic drugs, as well as the evolving requirements for biosimilar devices.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Stable Patient Satisfaction Found After Switching From the Humira or Biosimilar CT-P17
December 14th 2024A real-world study in France found patient satisfaction was stable after switching from either the reference product or a low-concentration adalimumab biosimilar to the adalimumab biosimilar CT-P17, a high-concentration, citrate-free formulation.
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.