Anar Dossa, director of Pharmacy Services at Pacific Blue Cross, discusses the company's involvement with British Columbia's biosimilars switching program.
In 2019, British Columbia (BC) became the first Canadian province to announce and implement a biosimilars switching initiative. Soon after, 3 other provinces developed their own plans to draw on biosimilars for health care savings. BC’s initiative introduced a mandatory switching policy from reference products to a select list of biosimilars. Each phase of the initiative is given a transition period, allowing physicians time to prepare patients for biosimilars before BC PharmaCare, the public health program, officially stops covering the reference products. The province recently concluded in its third phase, officially using etanercept, infliximab, rituximab, and insulin glargine biosimilars as the primary medications to treat a number of rheumatic conditions, such as ankylosing spondylitis and rheumatoid arthritis.
Pacific Blue Cross, one of the health plan providers in BC, has already seen success in aligning plan sponsors and members with the initiative, generating $27 million in savings by converting 99% of their plans. We sat down with Anar Dossa, director of Pharmacy Services at Pacific Blue Cross and leader of biosimilar transitions for the company’s benefits plan clients and members, to discuss company projections and challenges that have come with implementing the initiative.
To learn more about phase 3 of the BC Biosimilars Initiative, click here.
To learn more about recent biosimilar launches in Canada, click here or here.
To learn more about biosimilar switches in Canada, click here.
To learn more about other Canadian province’s biosimilar plans, click here.
To learn more about Pacific Blue Cross’s success with the program, click here.
Resolution of Injection Site Reactions After Switching to Adalimumab Biosimilar
February 22nd 2025A 15-year-old girl with ulcerative colitis who developed injection site reactions to the adalimumab reference product was successfully switched to the biosimilar LBAL without recurrence of symptoms, demonstrating the safety and effectiveness of switching for medical reasons, likely due to an allergic reaction to an excipient in the originator.
Biosimilars in Action: Market Shifts, Legal Insights, and FDA Approvals
February 9th 2025In this episode of Not So Different, host Skylar Jeremias covers the latest biosimilar developments, including new FDA approvals, patent disputes, and biosimilar market trends shaping the health care landscape.
Disease Activity, Safety Remain Following Switch From Infliximab Biosimilar to Remicade in IBD
February 15th 2025Switching back from infliximab biosimilar SB2 to reference infliximab (Remicade) did not affect clinical disease activity or safety in inflammatory bowel disease (IBD), according to a prospective cohort study.
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.