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Switching to biosimilars: current perspectives in immune-mediated inflammatory diseases
Christopher J Edwards1, Jana Hercogová2, Helene Albrand3
1NIHR Clinical Research Facility, University Hospital Southampton NHS Foundation Trust , Southampton , UK.
Biosimilars offer wider access to immune-mediated inflammatory disease treatments. Switching stable patients from reference biologics to biosimilars is increasingly accepted with growing evidence and open communication.
Area of Science:
- Immunology
- Pharmacoeconomics
- Gastroenterology
Background:
- Patent expiries of biologics have led to the development of biosimilars.
- Biosimilars offer potential for broader patient access to therapies for immune-mediated inflammatory diseases (IMIDs).
- While initiating biosimilars in treatment-naïve patients is accepted, switching stable patients requires careful consideration.
Purpose of the Study:
- To discuss considerations for switching patients with IMIDs from reference biologics to biosimilars.
- To review clinical data and real-world experience regarding biosimilar switching.
- To explore physician and patient perspectives, medical society stances, and communication strategies.
Main Methods:
- Review of clinical trial data and real-world evidence on biosimilar switching in IMIDs.
- Analysis of medical society positions on biosimilar use.
- Discussion of patient-physician communication and shared decision-making.
Main Results:
- Growing evidence supports the safety and efficacy of switching from reference biologics to biosimilars.
- Physician and patient acceptance of switching is increasing with accumulating real-world data.
- Effective patient-physician communication is crucial for successful switching.
Conclusions:
- Biosimilars enhance treatment accessibility and financial sustainability for IMID therapies.
- Increased real-world evidence is expected to further boost acceptance of biosimilar initiation and switching.
- Shared decision-making and open communication are vital for patient confidence in biosimilar therapy.
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