EDP-938 Has a High Barrier to Resistance in Healthy Adults Experimentally Infected with Respiratory Syncytial Virus

被引:1
|
作者
Levene, Rachel Emily [1 ]
DeVincenzo, John [1 ]
Conery, Annie L. [1 ]
Ahmed, Alaa [1 ]
Or, Yat Sun [1 ]
Rhodin, Michael H. J. [1 ]
机构
[1] Enanta Pharmaceut Inc, 500 Arsenal St, Watertown, MA 02472 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2024年 / 231卷 / 02期
关键词
RSV; antiviral; antiviral resistance; clinical trials; challenge trial; N inhibitor; EDP-938; REVERSE GENETICS; INHIBITOR; MECHANISM; BURDEN; RISK; SITE;
D O I
10.1093/infdis/jiae471
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background EDP-938 is an oral once-daily RSV nucleoprotein (N) inhibitor with potent antiviral activity. In a human RSV challenge trial, EDP-938 significantly reduced viral load and symptom severity. During antiviral development, it is critical to understand the propensity for resistance to develop. In vitro studies of EDP-938 suggest a higher barrier to resistance as compared to RSV fusion inhibitors. We evaluated the development of viral resistance to EDP-938 in a human challenge trial.Methods A subset of the 124 participants with RSV infection were chosen for genetic analysis; 159 nasal wash samples from 48 participants were analyzed using next-generation sequencing of the N gene of RSV. Of the 48 participant sampled, 37 were from EDP-938-treated and 11 were placebo-treated participants, representing 45% and 26% of the participants, respectively. The effects of treatment-emergent mutations on viral load, EDP-938 efficacy, and viral fitness were evaluated.Results Two of the 37 EDP-938-treated participants with samples sequenced had treatment-emergent mutations: N:L139I and N:E112G. From in vitro analysis, N:L139I reduced sensitivity to EDP-938 by approximately 10-fold, while N:E112G had no effect. However, N:L139I was associated with a reduction in viral fitness, suggesting clinical resistance is associated with fitness costs. Neither of these variants were associated with reduced viral clearance.Conclusions In human RSV infections treated with EDP-938, emergence of RSV variants with reduced sensitivity to EDP-938 occurred in only 1 participant and was associated with reduced viral fitness. EDP-938's high barrier to resistance highlights its robust mechanism of action.Clinical Trials Registration NCT03691623. In an RSV human challenge trial only 1 participant had a treatment-emergent mutation associated with resistance to EDP-938. This resistance mutation was associated with reductions in viral fitness. Thus, EDP-938 has a high barrier to resistance.
引用
收藏
页码:e290 / e298
页数:9
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