Matt Harman talks about what employers can do to help promote biosimilar adoption in the United States, during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California.
Matt Harman is the senior director of pharmacy at Employers Health.
Transcript:
What role can employer groups play in getting more biosimilars to market?
Employers can be a big advocate for biosimilars when you think about the number of lives that are covered by employers in this country, [it’s] 60% of lives. And I think we need to help unify that voice as part of our work at the coalition to get employers to have that unified message. So, [when] you think about how specialty spend is growing, employers want to continue to provide benefits to their employees. They can do things by contacting their legislators and then showing that there is a real need, because we don't want manufacturers of biosimilars to exit the market because of things like the patent thickets that have delayed the launch of medications. If you look at all our employers [there are] very high levels of adoption of strategies in the specialty space. Under the traditional space, maybe a lower adoption [rate] because they just don't see that large savings numbers, and the growing trends in specialty have them anxious for biosimilars. So, I think having things that can help promote biosimilar adoption, [such as] maybe having grassroots alert emails [using] those template emails that you get to contact your legislature. [You can] make it easy for an employer to [insert] their name and send to their legislator if there's particular biosimilar legislation that could be beneficial. I think that would be a good initiative for employers, because they're anxious and they want to continue to provide benefits to their employees without the rise in specialties spending getting in the way of that.
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 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.
Q&A: Dr Kimberly Maxfield Explains How BsUFA III Will Advance the US Biosimilar Industry
December 20th 2023At AMCP Nexus, Kimberly Maxfield, PhD, pharmacologist at the FDA, delved into how the third reauthorization of the Biosimilar User Fee Act (BsUFA III) will shape the American biosimilar market and improve development efficiency over the next few years.
Breaking Barriers in Osteoporosis Care: New Denosumab Biosimilars Wyost, Jubbonti Approved
June 16th 2024In this episode, The Center for Biosimilars® delves into the FDA approval of the first denosumab biosimilars, Wyost and Jubbonti (denosumab-bbdz), and discuss their potential to revolutionize osteoporosis treatment with expert insights from 2 rheumatologists.