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Efficacy and Safety of Efdamrofusp Alfa versus Aflibercept in Participants with Neovascular Age-Related Macular Degeneration A Randomized, Double-Masked, Active-Controlled, Noninferiority, Phase II Trial

delete2025-02-01
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PRE
AI
J
Junran Sun
Y
Yanping Song
Y
Yuanyuan Gong
L
Liming Tao
H
Hong Wang
X
Xiangwen Shu
Y
Ying Wen
L
Ling Cui
J
Jian Ye
S
Shujie Lu
J
Junjie Deng
H
Haoyu Li
Y
Yihua Xu
L
Lei Qian
Z
Zhifeng Wu
Y
Yanlong Bi
Q
Qinghuai Liu
W
Wu, Miaoqin
J
Jinglin Zhang
J
Ji‐Long Hao
J
Jianping Tong
H
Hong Dai
赵明伟 (Mingwei Zhao)
J
Junfeng Mao
C
Chaopeng Li
T
Tao He
C
Cheng Pei
X
Xiaoling Liu
X
Xian Wang
M
Mingxin Li
W
Wei Wang
Q
Qinxiang Zheng
H
Huaijin Guan
H
Hui Peng
K
Ke Fan
W
Wenfang Zhang
朱丹 cover
朱丹 (Dan Zhu)
S
Songping Yu
W
Wenbin Wei
D
Ding Lin
J
Jinying Li
P
Peirong Lu
M
Ming Yan
W
W. Liu
H
Huixun Jia
X
Xiaodong Sun *
DOI:10.1016/j.oret.2024.08.014delete
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Abstract

Abstract

En 中文
Purpose: To evaluate efficacy and safety of efdamrofusp alfa compared with aflibercept in neovascular age-related macular degeneration (nAMD). Design: Randomized, double-masked, multicenter, active-controlled, noninferiority phase II study. Participants: A total of 231 treatment-naive and previously treated participants with active choroidal neovascularization secondary to nAMD were enrolled. Methods: Eligible participants were randomized (1:1:1) to 2 mg efdamrofusp alfa, 4 mg efdamrofusp alfa, or 2 mg aflibercept groups. Participants in all groups received 3 initial monthly loading doses, followed by treatment every 8 weeks, with assessment every 4 weeks up to week 52. Main Outcome Measures: The primary end point was the mean best-corrected visual acuity (BCVA) change from baseline to week 36. The prespecified noninferiority margin was set as-5 letters (80% confidence interval [CI]). Results: Each treatment group included 77 participants. The mean BCVA changes from baseline to week 36 for 2 mg efdamrofusp alfa, 4 mg efdamrofusp alfa and aflibercept groups were +10.6, +11.4, and +12.0 letters, respectively; least squares mean difference were-1.4 (80% CI:-3.5 to 0.7) between 2 mg efdamrofusp alfa and aflibercept, and-0.6 (80% CI:-2.7 to 1.6) between 4 mg efdamrofusp alfa and aflibercept. Mean central retinal thickness changes were consistent across groups. Adverse event rate was comparable among the groups. Conclusions: Efdamrofusp alfa demonstrated noninferiority to aflibercept in BCVA improvement, accompanied by a similar safety profile. Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article. Ophthalmology Retina 2025;9:156-165 (c) 2024 Published by Elsevier Inc. on behalf of the American Academy of Ophthalmology
Keywords:
Complement
Efdamrofusp alfa
Fibrosis
Macular atrophy
Neovascular age-related macular degeneration

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Ophthalmology Retina cover
Ophthalmology Retina
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