The United Kingdom's National Institute for Health Research (NIHR), part of the National Health Service (NHS), has created a website to educate the public about biosimilar drugs.
The United Kingdom's National Institute for Health Research (NIHR), part of the National Health Service (NHS), has created a website to educate the public about biosimilar drugs. The website, Focus on Biosimilars, explains the background of biologic drugs and the subsequent development of biosimilar drugs, which the NHS says, “may well hold the key to ensuring the sustainability of our globally renowned public healthcare system” because biosimilars can broaden access to expensive biologic treatments that would otherwise be denied to some patients.
Focus on Biosimilars is divided into 3 portals, one each for pharmaceutical companies, NHS healthcare professionals, and NHS patients and caregivers. The patient portal features interviews with patients, nurses, clinicians and pharmacists. These videos help to explain typical patient experiences with biosimilars, what switching programs are, how patients can benefit from clinical trials of biosimilars, as well as the definition of biosimilars and how they differ from originator biologics.
The 3 portals of Focus on Biosimilars explore many key questions associated with biosimilars in use by the NHS, including:
The website points out that uptake and acceptance of biosimilars has rapidly accelerated across the NHS in recent years. The site discusses the problem that lies with “The Usual Suspects” scenario, in which it is difficult to find clinicians interested in conducting clinical trials of biosimilars when “the usual contacts” among key medical research areas are not interested in participating in biosimilar trials. The NHS addressed this issue by having the NIHR Clinical Research Network (CRN) create biosimilar clinical trial packages that offer an alternative route to finding appropriate biosimilar study investigators and sites across the region.
The website also provides links to related information, including updates from the FDA and other international regulatory organizations, advice about local adoption of biosimilars, patient organizations and foundations, and links to information about how to participate in UK clinical trials of biosimilars.
Breaking Down Biosimilar Barriers: Interchangeability
November 14th 2024Part 3 of this series for Global Biosimilars Week, penned by Dracey Poore, director of biosimilars at Cardinal Health, explores the critical topic of interchangeability, examining its role in shaping biosimilar adoption and the broader implications for accessibility.
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.
Overcoming Challenges to Improve Access and Reduce Costs
November 12th 2024Biosimilars hold the potential to dramatically lower health care costs and improve access to life-changing treatments, but realizing this potential will require urgent policy reforms, market competition, and better education for both providers and patients.
Challenges, Obstacles, and Future Directions for Anti-TNF Biosimilars in IBD
November 9th 2024A review article on tumor necrosis factor (TNF)-α inhibitors in inflammatory bowel disease (IBD) outlined current use of anti-TNF originators and biosimilars, their efficacy and safety, the benefits and challenges of biosimilars, and the future of biosimilars in IBD.
Skyrizi Overtakes Humira: “Product Hopping” Leaves Biosimilar Market in Limbo
November 7th 2024For the first time, Skyrizi (risankizumab-rzaa) has replaced Humira (reference adalimumab) as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.