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
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
相关论文
共 26 条
  • [21] Safety and immunogenicity of a respiratory syncytial virus fusion glycoprotein F subunit vaccine in healthy adults: Results of a phase 1, randomized, observer-blind, controlled, dosage-escalation study
    Leroux-Roels, Geert
    De Boever, Fien
    Maes, Cathy
    Thi Lien-Anh Nguyen
    Baker, Sherryl
    Lopez, Antonio Gonzalez
    VACCINE, 2019, 37 (20) : 2694 - 2703
  • [22] A Phase 1 Randomized, Double-Blind, Placebo-Controlled Trial to Assess the Safety, Tolerability, and Pharmacokinetics of a Respiratory Syncytial Virus Neutralizing Monoclonal Antibody MK-1654 in Healthy Adults
    Aliprantis, Antonios O.
    Wolford, Dennis
    Caro, Luzelena
    Maas, Brian M.
    Ma, Hua
    Montgomery, Diana L.
    Sterling, Laura M.
    Hunt, Allen
    Cox, Kara S.
    Vora, Kalpit A.
    Roadcap, Brad A.
    Railkar, Radha A.
    Lee, Andrew W.
    Stoch, S. Aubrey
    Lai, Eseng
    CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2021, 10 (05): : 556 - 566
  • [23] Novel genetically-modified chimpanzee adenovirus and MVA-vectored respiratory syncytial virus vaccine safely boosts humoral and cellular immunity in healthy older adults
    Green, Christopher A.
    Sande, Charles J.
    Scarselli, Elisa
    Capone, Stefania
    Vitelli, Alessandra
    Nicosia, Alfredo
    Silva-Reyes, Laura
    Thompson, Amber J.
    de Lara, Catherine M.
    Taylor, Kathryn S.
    Haworth, Kathryn
    Hutchings, Claire L.
    Cargill, Tamsin
    Angus, Brian
    Klenerman, Paul
    Pollard, Andrew J.
    JOURNAL OF INFECTION, 2019, 78 (05) : 382 - 392
  • [24] Quantification of clesrovimab, an investigational, half-life extended, anti-respiratory syncytial virus protein F human monoclonal antibody in the nasal epithelial lining fluid of healthy adults
    Phuah, Jia Yao
    Maas, Brian M.
    Tang, Aimin
    Zhang, Ying
    Caro, Luzelena
    Railkar, Radha A.
    Swanson, Michael D.
    Cao, Yu
    Li, Hankun
    Roadcap, Brad
    Catchpole, Andrew P.
    Aliprantis, Antonios O.
    Vora, Kalpit A.
    BIOMEDICINE & PHARMACOTHERAPY, 2023, 169
  • [25] First-in-Human Randomized Study to Assess the Safety and Immunogenicity of an Investigational Respiratory Syncytial Virus (RSV) Vaccine Based on Chimpanzee-Adenovirus-155 Viral Vector-Expressing RSV Fusion, Nucleocapsid, and Antitermination Viral Proteins in Healthy Adults
    Cicconi, Paola
    Jones, Claire
    Sarkar, Esha
    Silva-Reyes, Laura
    Klenerman, Paul
    de Lara, Catherine
    Hutchings, Claire
    Moris, Philippe
    Janssens, Michel
    Fissette, Laurence A.
    Picciolato, Marta
    Leach, Amanda
    Gonzalez-Lopez, Antonio
    Dieussaert, Ilse
    Snape, Matthew D.
    CLINICAL INFECTIOUS DISEASES, 2020, 70 (10) : 2073 - 2081
  • [26] Safety and immunogenicity of novel respiratory syncytial virus (RSV) vaccines based on the RSV viral proteins F, N and M2-1 encoded by simian adenovirus (PanAd3-RSV) and MVA (MVA-RSV); protocol for an open-label, dose-escalation, single-centre, phase 1 clinical trial in healthy adults
    Green, C. A.
    Scarselli, E.
    Voysey, M.
    Capone, S.
    Vitelli, A.
    Nicosia, A.
    Cortese, R.
    Thompson, A. J.
    Sande, C. S.
    de Lara, Catherine
    Klenerman, P.
    Pollard, A. J.
    BMJ OPEN, 2015, 5 (10):