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Biosimilars Gastroenterology Roundup for May 2024—Podcast Edition
On this episode of Not So Different, we review the biggest gastroenterology biosimilar stories from May 2024, covering new data from conferences and journals on infliximab and adalimumab products that demonstrate positive clinical results and confirm the safety of these biosimilars, as well as the feasibility of switching to them.
On this episode of Not So Different, we review the biggest gastroenterology biosimilar stories from May 2024, covering new data from conferences and journals on infliximab and adalimumab products that demonstrate positive clinical results and confirm the safety of these biosimilars and the feasibility of switching to them.
Show notes
1. FDA Approves High-Concentration Cyltezo
3. DDW 2024 Posters Evaluate Safety, Efficacy, Impact of BMI on Zymfentra Use
4. Posters Demonstrate Switching Safety Between Originator, Biosimilar Infliximab in IBD
5. New Evidence Confirms Safe Biosimilar-to-Biosimilar Switching
6. Spanish Real-World Study: Adalimumab Biosimilar MSB11022 Safe, Effective in IBD
7. Data Show Promise for Adalimumab Biosimilars to Deliver on Safety, Cost Savings
8. Patients With IBD Experience Nocebo Effect Post Mandatory Switch to Biosimilar
9. Review: Product Attributes Relevant to Injection-Site Pain, Adalimumab Treatment
Functional Similarity Between Ustekinumab Biosimilar ABP 654, Stelara in Crohn Disease
January 18th 2025Functional similarity of the ustekinumab biosimilar ABP 654 (Wezlana) and the reference product (Stelara) was confirmed by a series of in vitro studies, which support the totality of evidence for the biosimliar's FDA approval.
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.
Cost-Efficiency in Action: Denmark's Transition to Biosimilar Adalimumab
January 14th 2025The nationwide mandatory switch from Humira (reference adalimumab) to biosimilar adalimumab in Denmark led to no increase in total health care costs over 9 months, with significant cost reductions for those who switched to GP2017 specifically, highlighting the economic feasibility of biosimilar adoption.
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.
