» Articles » PMID: 29553864

Analytical and Functional Similarity of Amgen Biosimilar ABP 215 to Bevacizumab

Overview
Journal MAbs
Date 2018 Mar 20
PMID 29553864
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

ABP 215 is a biosimilar product to bevacizumab. Bevacizumab acts by binding to vascular endothelial growth factor A, inhibiting endothelial cell proliferation and new blood vessel formation, thereby leading to tumor vasculature normalization. The ABP 215 analytical similarity assessment was designed to assess the structural and functional similarity of ABP 215 and bevacizumab sourced from both the United States (US) and the European Union (EU). Similarity assessment was also made between the US- and EU-sourced bevacizumab to assess the similarity between the two products. The physicochemical properties and structural similarity of ABP 215 and bevacizumab were characterized using sensitive state-of-the-art analytical techniques capable of detecting small differences in product attributes. ABP 215 has the same amino acid sequence and exhibits similar post-translational modification profiles compared to bevacizumab. The functional similarity assessment employed orthogonal assays designed to interrogate all expected biological activities, including those known to affect the mechanisms of action for ABP 215 and bevacizumab. More than 20 batches of bevacizumab (US) and bevacizumab (EU), and 13 batches of ABP 215 representing unique drug substance lots were assessed for similarity. The large dataset allows meaningful comparisons and garners confidence in the overall conclusion for the analytical similarity assessment of ABP 215 to both US- and EU-sourced bevacizumab. The structural and purity attributes, and biological properties of ABP 215 are demonstrated to be highly similar to those of bevacizumab.

Citing Articles

Preserved bevacizumab (Avastin®) eye drops for application in multidose containers - an in-vitro characterisation.

Lessiak U, Brandstoetter T, Nell B, Klein K, Mlynek G, Wimmer L BMC Vet Res. 2025; 21(1):129.

PMID: 40025446 PMC: 11871757. DOI: 10.1186/s12917-025-04592-4.


An Automated Tool for Glycosimilarity Assessment of mAb Therapeutic Biosimilars: Trastuzumab and Bevacizumab as Case Studies.

Shrivastava A, Patil S, Shah R, Rathore A BioDrugs. 2025; 39(2):333-345.

PMID: 39873867 DOI: 10.1007/s40259-025-00704-6.


Assessing Protein Content and Dimer Formation in the Bevacizumab Reference Product and Biosimilar Versions Marketed in Spain.

Oliva A, Echezarreta M, Santana-Mayor A, Conde-Diaz A, Goncalves J, Chow S Pharmaceutics. 2025; 16(12.

PMID: 39771500 PMC: 11728500. DOI: 10.3390/pharmaceutics16121520.


Comparison of Efficacy, Safety, and Economic Outcomes Between Biosimilar ABP 215 and Originator Bevacizumab in Japanese Patients With Colorectal Cancer.

Sumimoto T, Tanaka R, Tatsuta R, Kubota M, Itoh H Cureus. 2024; 16(10):e72260.

PMID: 39583480 PMC: 11584936. DOI: 10.7759/cureus.72260.


Real-world clinical efficacy of bevacizumab biosimilar in patients with advanced non-small-cell lung cancer.

Ou W, Hsu K, Tseng J, Lee P, Chen K, Huang Y Ther Adv Med Oncol. 2024; 16:17588359241290718.

PMID: 39483140 PMC: 11526195. DOI: 10.1177/17588359241290718.


References
1.
Goetze A, Liu Y, Zhang Z, Shah B, Lee E, Bondarenko P . High-mannose glycans on the Fc region of therapeutic IgG antibodies increase serum clearance in humans. Glycobiology. 2011; 21(7):949-59. DOI: 10.1093/glycob/cwr027. View

2.
Wang Y, Fei D, Vanderlaan M, Song A . Biological activity of bevacizumab, a humanized anti-VEGF antibody in vitro. Angiogenesis. 2005; 7(4):335-45. DOI: 10.1007/s10456-004-8272-2. View

3.
Schenauer M, Flynn G, Goetze A . Identification and quantification of host cell protein impurities in biotherapeutics using mass spectrometry. Anal Biochem. 2012; 428(2):150-7. DOI: 10.1016/j.ab.2012.05.018. View

4.
Hodoniczky J, Zheng Y, James D . Control of recombinant monoclonal antibody effector functions by Fc N-glycan remodeling in vitro. Biotechnol Prog. 2005; 21(6):1644-52. DOI: 10.1021/bp050228w. View

5.
Zhang Q, Goetze A, Cui H, Wylie J, Trimble S, Hewig A . Comprehensive tracking of host cell proteins during monoclonal antibody purifications using mass spectrometry. MAbs. 2014; 6(3):659-70. PMC: 4011910. DOI: 10.4161/mabs.28120. View