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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
Samsung Bioepis Report Showcases Adalimumab Biosimilar Growth in Market Share
October 11th 2024Adalimumab biosimilars have seen a significant increase in market share, from 2% in early 2024 to 22%, as payers and pharmacy benefit managers begin to prioritize these biosimilars over the reference product, Humira.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Eye on Pharma: EC Approved Ustekinumab; Zymfentra Expansion; Biosimilar Policy Briefing
September 26th 2024The European Commission (EC) approved Celltrion's ustekinumab biosimilar for chronic inflammatory diseases, Celltrion expanded access to Zymfentra (subcutaneous infliximab-dyyb) through partnerships with Cigna and Express Scripts, and the Association for Accessible Medicines held a policy briefing addressing barriers to biosimilar adoption.
French Study Finds High Patient Satisfaction With Adalimumab Biosimilar Treatment for IBD
September 21st 2024An observational study assessing patient satisfaction with adalimumab for inflammatory bowel disease (IBD) reported a high level of satisfaction with all adalimumab product, including biosimilars.
