A recent study found that enrollment in patient support programs was associated with greater adherence, improved persistence, and reduced medical and total healthcare costs for patients who were receiving adalimumab therapy.
Biologic drug developers often provide free-to-patient support programs (PSP) that assist patients with drug costs, injection training, or nurse support, but the impact of such programs for patients receiving adalimumab has not been assessed in the past. A recently published study sought to quantify the relationship between participation in a patient program and outcomes in patients who were initiating treatment with adalimumab.
The longitudinal, retrospective cohort study, funded by AbbVie (makers of the reference adalimumab, Humira), found that enrollment in patient support programs (PSP) was associated with greater adherence, improved persistence, and reduced medical and total healthcare costs for patients who were receiving adalimumab therapy.
The study used patient-level data derived from the Humira PSP and the Symphony Health Solutions’ administrative claims data for patients who initiated adalimumab treatment between January 2008 and June 2014. The enrolled patients were being treated for Crohn’s disease, ulcerative colitis, rheumatoid arthritis, psoriasis, psoriatic arthritis, or ankylosing spondylitis, and all were naïve to biologic treatment before initiating adalimumab.
Of the 2386 patients included in the study, 1199 patients were in the PSP cohort and 1187 in the non-PSP cohort. All patients were required to have evidence of medical and pharmacy coverage from at least 6 months before and after their first adalimumab claim and at least 12 months after an index date (which was assigned as the earliest date of PSP enrollment. Time to enrollment following treatment initiation was used to assign index dates to the non-PSP cohort).
The researchers found the following:
The authors concluded that PSP enrollment was associated with greater adherence, improved persistence, and reduced medical and total healthcare costs for patients who were receiving adalimumab therapy. These findings are important, they say, because existing evidence shows rates of nonadherence to anti-tumor necrosis factor therapies exceeds 40%; nonadherence limits effectiveness, is associated with poor clinical outcomes, and creates a substantial economic burden. While no consistent risk factors for nonadherence have been identified, evidence suggests that support programs increase adherence to chronic therapy regimens.
The authors also suggest that their data provide support for prescribing physicians to encourage patients to enroll in PSPs, as well as for pharmaceutical companies to further develop and invest in such programs.
The Banking of Biosimilars: Insights From a Leading Health Economist
February 4th 2025Biosimilars have the potential to reduce health care costs and expand patient access, but economic and policy barriers affect adoption, explored James D. Chambers, PhD, MPharm, MSc, associate professor at the Tufts Medical Center Institute for Clinical Research and Health Policy Studies, in an interview.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
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.
FDA Approves Celltrion's Avtozma as Third Tocilizumab Biosimilar
January 31st 2025The FDA approved Avtozma, a tocilizumab biosimilar developed by Celltrion, for the treatment of several rheumatic conditions. It is the third biosimilar to reference Actemra (tocilizumab) to be approved for US patients.