The prevalence of inflammatory bowel disease (IBD) among adults seems to be increasing significantly, yet there are signs that the utilization of biologics to treat patients with this chronic disease have plateaued.
The prevalence of inflammatory bowel disease (IBD) among adults seems to be increasing significantly, yet there are signs that the utilization of biologics to treat patients with this chronic disease have plateaued.
In the October 28, 2016 issue of Mortality Morbidity Weekly Review, researchers from the Centers for Disease Control and Prevention (CDC) announced the findings of its 2015 National Health Interview Survey on IBD. They estimated that the prevalence of IBD in the US adult population was 3.1 million (1.3% of the total US adult population). A similar study conducted in 1999 found the figure to be 1.8 million (or 0.9% of the adult US population), a 72% increase in number and a 44% increase by proportion of the population. According to the CDC, a dominating factor in this trend is a substantially higher prevalence of IBD identified among adults aged ≥45 years, mostly in Hispanics and non-Hispanic whites, and those in lower socioeconomic levels. The NHIS is based on the survey responses of more than 33,500 American adults.
This raises the question of whether the utilization of biologics used to treat IBD has also increased over this time. Remicade® was approved for use in 1998, and Humira® was approved in 2002 (the anti-TNF fusion protein etanercept was also approved in 1998, but is not indicated for IBD). These remain the two most commonly used agents to treat IBD, especially Crohn’s disease, with Cimzia® a distant third. Based on a single-center study from Stanford University, the utilization of biologics for adults and children with IBD has not increased proportionately. Use of Remicade® peaked in 2008, and utilization of Humira continued somewhat slow growth through 2012, the end of the data collection period. Interestingly, biologic use in IBD resulted in dramatic lowering of hospitalization costs, but not in the rate of abdominal surgery in these patients. They attribute this finding to the possible erosion of drug efficacy when given chronically over the long term. However, the Stanford researchers also found that pharmaceutical therapy in IBD, particularly Crohn’s disease, is the primary cost component in health care expenditures. “Pharmacy utilization costs account for nearly one-half (45.5%) of the total CD-attributable costs, exceeding inpatient care costs. Anti-TNF agents alone comprised nearly one-third (29.5%) of total costs,” they said.
The question of whether the biologic utilization pie is growing, shrinking, or remaining the same could have implications for the brand new biosimilar market for IBD.
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 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.
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
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.
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.
Subcutaneous Infliximab CT-P13 Superior to Placebo as Maintenance Therapy for IBD
November 16th 2024In 2 randomized controlled trials of maintenance therapy for inflammatory bowel disease (IBD), the subcutaneous formulation of the infliximab biosimilar CT-P13 demonstrated superiority to placebo in patients with Crohn disease and ulcerative colitis.