Aflibercept Biosimilar MYL-1701P vs Reference Aflibercept in Diabetic Macular Edema
Susan B. Bressler, Abhijit Barve, Prasanna C. Ganapathi, Katrin Beckmann, Rajendra S. Apte, Dennis M. Marcus, Kristīne Baumane, Somesh Agarwal, Piotr Oleksy, David A. Reichstein, Sunil S. Patel, Jan Ernest, Rózsa Dégı̀, Vishali Gupta, Genichiro Kishino, Motohiro Kamei, Subramanian Loganathan, INSIGHT Study Group, Nauman Chaudhry, David A. Reichstein, Ali Tabassian, Howard F. Fine, Raymond N. Sjaarda, Dennis M. Marcus, Mark Barakat, Pravin U. Dugel, David Eichenbaum, Amr Dessouki, Adam Berger, BRYAN N. ANGLE, Margaret Chang, Sunil Patel, David M. Brown, Allen B. Thach, Carl W. Baker, Alan J Gordon, Sam E. Mansour, Gregory M Fox, D. Virgil Alfaro, John B. Davies, Ghassan R Ghorayeb, Glenn Stoller, Thomas Mark Johnson, Jan Němčanský, J Řehák, Jan Studnička, Jan Ernest, Vladimír Korda, Miroslav Veith, Daniel Krzyzanek, B Kalvodová, Pavel Stodůlka, Nicolas Feltgen, Katrin Lorenz PD, Salvatore Grisanti, Maria Andreea Gamulescu, Ulrich Kellner, Walter Sekundo, Claudia Dahlke, Oliver Zeitz, Kristīne Baumane, Guna Laganovska, Signe Ozolina, Attila Vajas, András Seres, Alexis Tsorbatzoglou, Judit Radnoti, Katalin Kiss, Katalin Gombos, Rózsa Dégı̀, Balázs Varsányi, Ágnes Kerényi, Sumiyo Noge, Tomoyuki Muramatsu, T. Kaga, Hideyasu Oh, Miki Watanabe, Yuji Oshima, Hideaki Fujita, Genichiro Kishino, Tsukasa Hanemoto, Kōji Murata, Takashi Kitaoka, Isao Saito, Teruyo Tanabe, Nobuyuki Ebihara, Hiroko Imaizumi, Kiyoshi Ishii, Motohiro Kamei, Minoru Furuta, Akira Ojima, Osamu Sawada, Tsutomu Kawasaki, Hiroshi Otake, Norihito Doi, Keitetsu Abe, Satoshi Matsuda, Namie Kobayashi, Yuki Yoshizumi, M V Budzinskaya
Abstract
Importance: Biosimilars may be lower-cost alternatives to originator biologic products, potentially offering expanded access or reduced economic burden, but have not been evaluated with aflibercept in diabetic macular edema (DME). Objective: To compare efficacy and safety of MYL-1701P, an aflibercept biosimilar, with reference aflibercept (Eylea [Regeneron]) in DME. Design, Setting, and Participants: This was a double-masked, randomized clinical trial that included participants at 77 centers across the US, Europe, Japan, and India. Included in the analysis were individuals 18 years and older with type 1 or type 2 diabetes with central DME and best-corrected visual acuity (BCVA) letter score of 73 to 38 in the study eye using an Early Treatment Diabetic Retinopathy Study (ETDRS) chart. Study data were analyzed from October to December 2021. Interventions: Formulations of MYL-1701P (0.5-mg vial) or reference aflibercept every 4 weeks for 5 consecutive intravitreal injections, followed by every 8 weeks through week 52. Main Outcomes and Measures: The primary outcome was the adjusted difference in least squares mean (SE) change from baseline BCVA letter score at week 8 with an equivalence margin of -3 to +3 letters. Secondary outcomes included change in central subfield thickness (CST), BCVA, number of injections over 52 weeks, incidence of adverse events (AEs), and antidrug antibodies (ADAs). Results: A total of 355 participants (mean [SD] age, 62.2 [9.2] years; 216 male [60.8%]) were randomized to MYL-1701P (179 participants [50.4%]) and aflibercept (176 participants [49.6%]). At week 8, mean (SE) change in BCVA was 6.60 (0.55) letters vs 6.56 (0.55) letters in the MYL-1701P vs aflibercept groups. The adjusted mean difference of 0.04 letters (90% CI, -1.16 to 1.24 letters) met the primary outcome. At week 8, mean (SE) change in CST was -112 (7) μm vs -124 (7) μm in the MYL-1701P vs aflibercept groups (adjusted mean difference, 12 μm; 90% CI, -3 to 26 μm). The incidence of treatment-emergent AEs in the MYL-1701P and aflibercept arms were ocular (30.9% [55 of 178] vs 29.5% [52 of 176]), serious ocular (0.6% [1 of 178] vs 1.1% [2 of 176]), nonocular (65.2% [116 of 178] vs 65.3% [115 of 176]), and serious nonocular (16.9% [30 of 178] vs 11.9% [21 of 176]). The mean (SD) total number of injections was 8.4 (2.1) vs 8.7 (1.8) in the MYL-1701P vs aflibercept groups. The incidence of treatment-induced or treatment-boosted ADAs was 2.8% (5 of 177) vs 5.7% (10 of 176) in the MYL-1701P vs aflibercept arms. Conclusions and Relevance: MYL-1701P demonstrated clinical equivalence in regard to efficacy, with comparable safety and immunogenicity, to reference aflibercept. These findings support use of MLY-1701P as an alternative to reference aflibercept. Trial Registration: ClinicalTrials.gov Identifier: NCT03610646.