SB8, an approved bevacizumab biosimilar based on totality of evidence: scientific justification of extrapolation

Author:

Peeters Marc1,Lipp Hans-Peter2,Park Minjeong3,Yoon Ye Chan3,Arnold Dirk4

Affiliation:

1. Antwerp University Hospital, 2650, Edegem, Belgium

2. University Hospital Tübingen, 72076, Tübingen, Germany

3. Samsung Bioepis Co., Ltd, Incheon, 21987, Republic of Korea

4. Asklepios Tumorzentrum Hamburg, AK Klinik Altona, 22763, Hamburg, Germany

Abstract

SB8 is a biosimilar of bevacizumab based on its similarity demonstrated by physicochemical, functional, non-clinical and clinical studies. Supported by the concept of extrapolation, SB8 was authorized and is used in a similar manner across all types of tumors as reference bevacizumab. Furthermore, SB8 offers convenience with prolonged stability compared with reference bevacizumab in diluted form. Although a biosimilar must demonstrate biosimilarity to a reference product with the ‘totality of evidence’ in a stringent regulatory process for marketing authorization, some concerns remain among healthcare practitioners, particularly about extrapolation. This review summarizes the concepts of the totality of evidence and extrapolation in biosimilar development and the role of bevacizumab biosimilars in the management of metastatic colorectal cancer as an extrapolated indication.

Funder

Samsung Bioepis

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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