Temporal Trends in the Prescription of Biosimilars and the Status of Switching from Original Biologics to Biosimilars at Individual and Institutional Levels in Japan
- PMID: 40770534
- DOI: 10.1007/s43441-025-00850-7
Temporal Trends in the Prescription of Biosimilars and the Status of Switching from Original Biologics to Biosimilars at Individual and Institutional Levels in Japan
Abstract
Purpose: To describe the temporal trends in the prescription of biologics in Japan, with additional analysis focusing on switching from original biologics to biosimilars at the individual and institutional levels.
Methods: Using the JMDC claims database from January 2005 to May 2024, we identified patients who received at least one prescription for 17 biologics (original biologics or biosimilars). We elucidated the monthly trends in the proportions of original biologics and biosimilars. We also estimated the proportion of patients receiving original biologics only, those receiving biosimilars only, and those switching from original biologics to biosimilars (and vice versa) during the study period. Finally, we estimated the proportion of medical institutions that started prescribing biosimilars during the study period based on the type of medical institution.
Results: Temporal trends in the proportions of original biologics and biosimilars varied widely. In May 2024, the proportion of biosimilar prescriptions was 13.6% for somatropin and 92.5% for filgrastim. At the individual level, the proportion of patients switching from original biologics to biosimilars was low (1.2-14.0%), indicating that switches do not often occur within the same patient, while more recent new users of biologics start biosimilars. At the institutional level, university-related hospitals and clinics were more and less likely, respectively to introduce biosimilars than public and other types of hospitals.
Conclusion: Temporal trends in the prescription of biosimilars and switching patterns varied widely by the type of biologics. The type of medical institution should be considered when assessing and promoting the use of biosimilars. Further research and strategies to increase the use of biosimilars in clinics may be needed.
Keywords: Administrative claims; Biological products; Biosimilar pharmaceuticals; Drug utilization; Pharmacoepidemiology.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Conflict of interest: HM received consulting fees from GlaxoSmithKline K.K., Nippon Boehringer Ingelheim Co., Ltd., Novartis Pharma K.K., Janssen Pharmaceutical K.K., Biogen Japan Ltd., Takeda Pharmaceutical Co., Ltd., TEIJIN Pharma Ltd., Hisamitsu Pharmaceutical Co., Inc., and Otsuka Pharmaceutical Co., Ltd. RS received consulting fees from Nippon Kayaku Co. Ltd. MI’s Department of Digital Health, Institute of Medicine, University of Tsukuba, is conducting joint research with JMDC Inc., with funding from JMDC Inc. The funders played no role to conduct the present study.
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