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A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis

INTRODUCTION: YLB113 is a biosimilar of the reference product (RP), etanercept, under development for treatment of patients with moderate-to-severe rheumatoid arthritis (RA) and other approved indications. A phase 3 study was conducted in Europe, Japan, and India to compare the efficacy, safety, and...

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Autores principales: Yamanaka, Hisashi, Kamatani, Naoyuki, Tanaka, Yoshiya, Hibino, Toshihiko, Drescher, Edit, Sánchez-Bursón, Juan, Rettenbacher, Manfred, Bhatia, Girish, Gadve, Snehal, Shah, Chirag, Bakhle, Dhananjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021908/
https://www.ncbi.nlm.nih.gov/pubmed/31833011
http://dx.doi.org/10.1007/s40744-019-00186-3
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author Yamanaka, Hisashi
Kamatani, Naoyuki
Tanaka, Yoshiya
Hibino, Toshihiko
Drescher, Edit
Sánchez-Bursón, Juan
Rettenbacher, Manfred
Bhatia, Girish
Gadve, Snehal
Shah, Chirag
Bakhle, Dhananjay
author_facet Yamanaka, Hisashi
Kamatani, Naoyuki
Tanaka, Yoshiya
Hibino, Toshihiko
Drescher, Edit
Sánchez-Bursón, Juan
Rettenbacher, Manfred
Bhatia, Girish
Gadve, Snehal
Shah, Chirag
Bakhle, Dhananjay
author_sort Yamanaka, Hisashi
collection PubMed
description INTRODUCTION: YLB113 is a biosimilar of the reference product (RP), etanercept, under development for treatment of patients with moderate-to-severe rheumatoid arthritis (RA) and other approved indications. A phase 3 study was conducted in Europe, Japan, and India to compare the efficacy, safety, and immunogenicity of YLB113 with the RP over a treatment period of 52 weeks. METHODS: Overall, 528 patients with moderate-to-severe RA receiving concomitant methotrexate were randomized to receive a once-weekly, subcutaneous dose of 50 mg YLB113 or the RP. The primary endpoint was ACR20 response rate at week 24, with similarity confirmed if the 95% confidence interval (CI) for YLB113 and the RP was within the range of − 15 to 15%. Safety and immunogenicity endpoints were assessed to week 52. RESULTS: Based on the European analysis, in the full analysis set, ACR20 response at week 24 was 83.3% and 88.5% for YLB113 and the RP, respectively. Responses were within the predefined clinical equivalence margin. The sensitivity analysis in the per protocol set revealed a similar proportion of subjects exhibiting ACR20 response at week 24 between groups, with a difference of − 5.1% (95% CI − 11.07 to 0.81). The incidence of treatment-emergent adverse events was comparable between groups, and the incidence of antidrug antibody development to week 24 favored YLB113 (0.8 vs. 8.3%). CONCLUSIONS: This study demonstrated biosimilarity of YLB113 to the RP regarding efficacy, safety, and immunogenicity in patients with moderate-to-severe RA. Based on the same mechanism of action, biosimilarity could be extrapolated to other therapeutic indications approved for etanercept. TRIAL REGISTRATION: EudraCT Number: 2015-002,809-12. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40744-019-00186-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-70219082020-02-28 A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis Yamanaka, Hisashi Kamatani, Naoyuki Tanaka, Yoshiya Hibino, Toshihiko Drescher, Edit Sánchez-Bursón, Juan Rettenbacher, Manfred Bhatia, Girish Gadve, Snehal Shah, Chirag Bakhle, Dhananjay Rheumatol Ther Original Research INTRODUCTION: YLB113 is a biosimilar of the reference product (RP), etanercept, under development for treatment of patients with moderate-to-severe rheumatoid arthritis (RA) and other approved indications. A phase 3 study was conducted in Europe, Japan, and India to compare the efficacy, safety, and immunogenicity of YLB113 with the RP over a treatment period of 52 weeks. METHODS: Overall, 528 patients with moderate-to-severe RA receiving concomitant methotrexate were randomized to receive a once-weekly, subcutaneous dose of 50 mg YLB113 or the RP. The primary endpoint was ACR20 response rate at week 24, with similarity confirmed if the 95% confidence interval (CI) for YLB113 and the RP was within the range of − 15 to 15%. Safety and immunogenicity endpoints were assessed to week 52. RESULTS: Based on the European analysis, in the full analysis set, ACR20 response at week 24 was 83.3% and 88.5% for YLB113 and the RP, respectively. Responses were within the predefined clinical equivalence margin. The sensitivity analysis in the per protocol set revealed a similar proportion of subjects exhibiting ACR20 response at week 24 between groups, with a difference of − 5.1% (95% CI − 11.07 to 0.81). The incidence of treatment-emergent adverse events was comparable between groups, and the incidence of antidrug antibody development to week 24 favored YLB113 (0.8 vs. 8.3%). CONCLUSIONS: This study demonstrated biosimilarity of YLB113 to the RP regarding efficacy, safety, and immunogenicity in patients with moderate-to-severe RA. Based on the same mechanism of action, biosimilarity could be extrapolated to other therapeutic indications approved for etanercept. TRIAL REGISTRATION: EudraCT Number: 2015-002,809-12. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40744-019-00186-3) contains supplementary material, which is available to authorized users. Springer Healthcare 2019-12-12 /pmc/articles/PMC7021908/ /pubmed/31833011 http://dx.doi.org/10.1007/s40744-019-00186-3 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Yamanaka, Hisashi
Kamatani, Naoyuki
Tanaka, Yoshiya
Hibino, Toshihiko
Drescher, Edit
Sánchez-Bursón, Juan
Rettenbacher, Manfred
Bhatia, Girish
Gadve, Snehal
Shah, Chirag
Bakhle, Dhananjay
A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
title A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
title_full A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
title_fullStr A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
title_full_unstemmed A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
title_short A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
title_sort comparative study to assess the efficacy, safety, and immunogenicity of ylb113 and the etanercept reference product for the treatment of patients with rheumatoid arthritis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021908/
https://www.ncbi.nlm.nih.gov/pubmed/31833011
http://dx.doi.org/10.1007/s40744-019-00186-3
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