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Published in: Advances in Therapy 10/2020

Open Access 01-10-2020 | Bevacizumab | Original Research

Evaluation of the Physico-Chemical and Biological Stability of SB8 (Aybintio), a Proposed Biosimilar to Bevacizumab, Under Ambient and In-Use Conditions

Authors: Dongkuk Park, Jihyun Kim, Jihoon Yun, Su Jin Park

Published in: Advances in Therapy | Issue 10/2020

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Abstract

Introduction

No stability data of SB8 (proposed biosimilar to bevacizumab) are available for opened vials at 2–8 °C or for unopened vials stored outside of this range. Furthermore, limited stability data are available for dilutions. Stability of unopened vials of SB8 at ambient temperature and in-use stability for opened vials as well as diluted SB8 in infusion bags were evaluated.

Methods

SB8 stability was assessed in three scenarios in the absence of light: unopened 100-mg vials 36 months after manufacture stored at 30 ± 2 °C with 65 ± 5% relative humidity for 1 month, opened 100-mg and 400-mg vials stored at 5 ± 3 °C for 72 h and diluted (1.4 mg/ml or 16.5 mg/ml in 100 ml 0.9% NaCl polyolefin bags) stored for 45 days at 5 ± 3 °C and then 3 days at 30 ± 2 °C; the United Kingdom’s National Health Service protocol was used for the study design after dilution. Physicochemical stability (appearance, pH, protein concentration, size-exclusion high-performance liquid chromatography, non-reducing capillary electrophoresis-sodium dodecyl sulfate, imaged capillary isoelectric focusing), biological activity [vascular endothelial growth factor (VEGF) neutralization assay, VEGF binding assay] and potential safety impact properties (subvisible particulates, submicronic aggregation by dynamic light scattering) were determined.

Results

All stability-indicating criteria including those for biological activity were met for both unopened vials at ambient condition and for in-use conditions of opened vials as well as both dilutions. No noteworthy changes in terms of physicochemical stability, biological activity and properties with a potential safety impact occurred.

Conclusion

Under the studied aspetic extreme conditions, SB8 was stable. Our data may support advanced SB8 preparation and may help prevent SB8 wastage because of exceptional temperature excursions or unused product. Sterility assurance is the responsibility of the user and is of utmost importance when opened or diluted SB8 is not immediately used.
Literature
3.
go back to reference Reck M, Luft A, Bondarenko I, Shevnia S, Trukhin D, Kovalenko NV, et al. A phase III, randomized, double-blind, multicenter study to compare the efficacy, safety, pharmacokinetics, and immunogenicity between SB8 (proposed bevacizumab biosimilar) and reference bevacizumab in patients with metastatic or recurrent nonsquamous non-small cell lung cancer. Lung Cancer. 2020;146:12–8.CrossRef Reck M, Luft A, Bondarenko I, Shevnia S, Trukhin D, Kovalenko NV, et al. A phase III, randomized, double-blind, multicenter study to compare the efficacy, safety, pharmacokinetics, and immunogenicity between SB8 (proposed bevacizumab biosimilar) and reference bevacizumab in patients with metastatic or recurrent nonsquamous non-small cell lung cancer. Lung Cancer. 2020;146:12–8.CrossRef
6.
go back to reference Pivot X, Bondarenko I, Nowecki Z, Dvorkin M, Trishkina E, Ahn JH, et al. A phase III study comparing SB3 (a proposed trastuzumab biosimilar) and trastuzumab reference product in HER2-positive early breast cancer treated with neoadjuvant-adjuvant treatment: final safety, immunogenicity and survival results. Eur J Cancer. 2018;93:19–27.CrossRef Pivot X, Bondarenko I, Nowecki Z, Dvorkin M, Trishkina E, Ahn JH, et al. A phase III study comparing SB3 (a proposed trastuzumab biosimilar) and trastuzumab reference product in HER2-positive early breast cancer treated with neoadjuvant-adjuvant treatment: final safety, immunogenicity and survival results. Eur J Cancer. 2018;93:19–27.CrossRef
7.
go back to reference Vigneron J, D’Huart E, Demoré B. Stability studies in oncology. Eur J Oncol Pharm. 2019;2(2):e12.CrossRef Vigneron J, D’Huart E, Demoré B. Stability studies in oncology. Eur J Oncol Pharm. 2019;2(2):e12.CrossRef
9.
go back to reference International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use. Validation of analytical procedures: text and methodology Q2(R1). 1994. International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use. Validation of analytical procedures: text and methodology Q2(R1). 1994.
13.
go back to reference Vlasak J, Ionescu R. Fragmentation of monoclonal antibodies. MAbs. 2011;3(3):253–63.CrossRef Vlasak J, Ionescu R. Fragmentation of monoclonal antibodies. MAbs. 2011;3(3):253–63.CrossRef
14.
go back to reference Herrmann JE, Collins MF. Quantitation of immunoglobulin adsorption to plastics. J Immunol Methods. 1976;10(4):363–6.CrossRef Herrmann JE, Collins MF. Quantitation of immunoglobulin adsorption to plastics. J Immunol Methods. 1976;10(4):363–6.CrossRef
Metadata
Title
Evaluation of the Physico-Chemical and Biological Stability of SB8 (Aybintio), a Proposed Biosimilar to Bevacizumab, Under Ambient and In-Use Conditions
Authors
Dongkuk Park
Jihyun Kim
Jihoon Yun
Su Jin Park
Publication date
01-10-2020
Publisher
Springer Healthcare
Keyword
Bevacizumab
Published in
Advances in Therapy / Issue 10/2020
Print ISSN: 0741-238X
Electronic ISSN: 1865-8652
DOI
https://doi.org/10.1007/s12325-020-01465-0

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