During the 83rd Annual Scientific Meeting of the American College of Gastroenterology, researchers from the United Kingdom reported on yet another large, nonmedical switch from reference infliximab to biosimilar CT-P13 (Inflectra, Remsima), this time in the Pennine Acute Hospitals Trust.
In the United Kingdom, where switching patients to biosimilars has become more common as National Health Service trusts seek to benefit from cost savings, multiple reports have noted the feasibility of switching patients to biosimilar infliximab.
During the 83rd Annual Scientific Meeting of the American College of Gastroenterology, researchers from the United Kingdom reported on yet another large, nonmedical switch from reference infliximab to biosimilar CT-P13 (Inflectra, Remsima), this time in the Pennine Acute Hospitals Trust.
The research team, led by Anirudh Pramod Bhandare, MBBS, MD, performed a retrospective review of patients with inflammatory bowel disease who were switched from the reference product to the biosimilar, and analyzed disease demographics, the clinical course of disease, and outcomes until the time of the last follow-up.
In total, 96 patients were switched, 44 of whom had ulcerative colitis (UC) and 52 of whom had Crohn disease (CD). The mean age at diagnosis was 34.73 years. The mean duration of treatment with the reference was 49.8 months, and the mean duration of treatment with the biosimilar at the time of the review was 7.9 months.
At the time of the switch, 76 patients had normal C-reactive protein (CRP) levels, while 15 patients had elevated levels. At follow-up, 14 patients had an increase in CRP. Eighty patients remained in biochemical remission.
In 31 patients, therapeutic drug monitoring was performed. In 28 patients, infliximab was maintained in the therapeutic range, while 3 patients required dose intensification.
At the time of the last follow-up, 72 patients (34 with UC and 38 with CD) were in clinical remission, and 31 patients (13 with UC and 18 with CD) had achieved mucosal healing.
The investigators concluded that biosimilar infliximab was well tolerated and maintained efficacy in patients who switched, which indicates that switching can “fulfill the purported aims of improving access to treatment and reducing costs.”
Reference
Bhandare AP, Nigam GB, Nayeemudin S, Limdi JK. Efficacy and tolerability of a biosimilar infliximab switch—a large single-centre experience from the U.K. Presented at the 83rd Annual Scientific Meeting of the American College of Gastroenterology, October 5-10, 2018; Philadelphia, Pennsylvania. Abstract 676. https://www.nature.com/articles/s41395-018-0296-0.pdf.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
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.
Breaking Down Biosimilar Barriers: Payer and PBM Policies
November 13th 2024Part 2 of this series for Global Biosimilars Week dives into the complexities of payer and pharmacy benefit manager (PBM) policies, how they impact biosimilar accessibility, and how addressing these issues may look under a second Trump term.
Biosimilars Gastroenterology Roundup for May 2024—Podcast Edition
June 2nd 2024On this episode of Not So Different, we review the biggest gastroenterology biosimilar stories from May 2024, covering new data from conferences and journals on infliximab and adalimumab products that demonstrate positive clinical results and confirm the safety of these biosimilars, as well as the feasibility of switching to them.
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.