In 2018, Green Shield Canada launched its pilot Biosimilar Transition Program, through 3 plan sponsors, under which patients already receiving biologics were switched to biosimilars. Now that the pilot is complete, the payer is calling the program a success.
In 2016, not-for-profit health benefits company Green Shield Canada (GSC) started to give biosimilars preferred product listings on its formularies, covering reference biologics only in exceptional circumstances for patients who were new to biologic therapy. Then, in 2018, GSC launched a pilot Biosimilar Transition Program, through 3 plan sponsors, under which patients already receiving biologics were switched to biosimilars. Now that the pilot is complete, the payer is calling the program a success.
Patients who were members of the 3 sponsored plans and who were receiving reference infliximab or etanercept therapy were sent letters explaining the pilot program and detailing 2 available options. First, patients could proceed with the one-time switch to biosimilar infliximab or etanercept after discussing it with their prescriber. Second, they could continue to receive their originator biologic and pay the difference in cost between the 2 drugs out-of-pocket.
In total, 41% of members opted to switch to a biosimilar, while 26% chose to remain on the originator product and pay the difference in cost. Another 9% were approved to continue on the originator product after providing clinical justification, while 3% changed to a different treatment entirely for reasons unrelated to the program (the final 21% of patients had not yet submitted a claim at the time of the pilot’s conclusion). GSC’s analysis shows an average savings of $8500 ($6395 USD) per member per year under the program.
GSC notes that, while it originally launched the pilot with the goal of a 60-day timeline to the switch, it amended that goal to 90 days based on feedback from plan sponsors.
It also notes that it partnered with HealthForward, a payer service provider that has dedicated care-coordinator nurses who follow a case management process to provide patients with the assistance that they need. The nurses ensured that there was contact with the patient at 1 month, 3 months, and 6 months to address any issues or answer questions, and HealthForward provided a dedicated phone line for patient support.
GSC says that there were no unexpected questions or concerns during the pilot; most patients were receptive to the switch, and some had even considered switching to a biosimilar prior to the pilot program’s commencement.
Questions asked by patients included the rationale for the change, the cost difference between the products, the efficacy of the biosimilar, and next steps for switching. Among patients who had concerns about the efficacy of the biosimilar, “Their concerns were satisfactorily addressed by the HealthForward care-coordinator nurses,” says GSC in a statement on the program.
On the heels of the successful pilot, GSC is opening the program to any plan sponsor who wants to take part.
Escaping the Void: All Things Biosimilars With Craig & G
May 4th 2025To close out the Festival of Biologics, Craig Burton and Giuseppe Randazzo from the Association for Accessible Medicines and the Biosimilars Council tackle the current biosimilar landscape and how the industry can emerge from the "biosimilar void."
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Eye on Pharma: Interchangeability Labels and Expanded Biosimilar Partnerships
May 29th 2025The FDA designates 2 biosimilars as interchangeable, enhancing access to treatments for inflammatory diseases and multiple sclerosis, while 2 other companies expand their biosimilar partnership to include more products.