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A New Biosimilar to Remicade in the Fray
Scientists at the FDA have provided their recommendation to be submitted to an independent medical advisory panel that will decide the fate of Remsima.
The market value of Remicade, Enbrel, and Humira could dwindle if Celltrion’s biosimilar to Remicade—deemed “highly similar” to the reference product by the FDA—is approved.
According to a news report by Reuters, scientists at the FDA provided their recommendation to be submitted to an independent medical advisory panel that will decide the fate of Remsima for rheumatoid arthritis and inflammatory bowel conditions like Crohn’s disease. The panel will recommend, or not, the biosimilar developed through a collaboration between Pfizer and Celltrion.
The scientists state in their report that Remsima is highly similar to Remicade in treating rheumatoid arthritis and ankylosing spondylitis, and that there are only minor differences in clinically inactive components.
If approved, this will be just the second biosimilar to enter the market after Zarxio, which was approved late last year. While a lot remains unknown in the field—naming, physician awareness, reimbursement policies for the follow-on biological—there’s definitely no turning back.
Exploring Racial, Ethnic Disparities in Cancer Care Prior Authorization Decisions
October 24th 2024On this episode of Managed Care Cast, we're talking with the author of a study published in the October 2024 issue of The American Journal of Managed Care® that explored prior authorization decisions in cancer care by race and ethnicity for commercially insured patients.
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Bridging the Vaccination Gap: Insights on Global Immunization Challenges
July 30th 2024On this episode of Managed Care Cast, we speak with Jeffery A. Goad, PharmD, MPH, 2024-2025 president of the National Foundation for Infectious Diseases, on the recent report from the World Health Organization and UNICEF on public immunization rates, with national and global health implications.
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