Safety, Tolerability, and Pharmacokinetics of a Novel Anti-Influenza Agent ZX-7101A Tablets in Healthy Chinese Participants: A First-in-Human Phase I Clinical Study

被引:0
作者
Wu, Junzhen [1 ]
Wei, Qiong [1 ]
Jin, Yi [1 ]
Cao, Guoying [1 ]
Yu, Jicheng [1 ]
Wu, Xiaojie [1 ]
Yang, Xinyi [1 ]
Li, Yilin [2 ]
Liu, Mei [2 ]
Qin, Xiaoli [2 ]
Ai, Jingwen [3 ,4 ]
Wang, Yin [2 ]
Zhang, Wenhong [3 ,4 ]
Zhang, Jing [1 ,5 ,6 ,7 ,8 ]
机构
[1] Fudan Univ, Huashan Hosp, Clin Pharmacol Res Ctr, Shanghai, Peoples R China
[2] Nanjing Zenshine Pharmaceut Co Ltd, Nanjing, Peoples R China
[3] Fudan Univ, Huashan Hosp, Natl Med Ctr Infect Dis, Shanghai, Peoples R China
[4] Fudan Univ, Huashan Hosp, Dept Infect Dis, Shanghai Key Lab Infect Dis & Biosafety Emergency, Shanghai, Peoples R China
[5] Fudan Univ, Huashan Hosp, Inst Antibiot, Shanghai, Peoples R China
[6] Key Lab Antibiot Clin Pharmacol Natl Hlth & Commis, Shanghai, Peoples R China
[7] Fudan Univ, Huashan Hosp, Natl Clin Res Ctr Aging & Med, Shanghai, Peoples R China
[8] Fudan Univ, Res Ward Huashan Hosp, Shanghai, Peoples R China
关键词
Influenza; ZX-7101A tablets; ZX-7101; Cap-dependent endonuclease inhibitor; Safety; Pharmacokinetics; INFLUENZA-A; VIRUS;
D O I
10.1016/j.ijantimicag.2024.107381
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: We investigated the safety, tolerability, and pharmacokinetics of ZX-7101A tablets, a novel cap-dependent endonuclease inhibitor, in healthy participants in a first-in-human study. Methods: The single ascending dose (SAD) part of the study included 40, 80, 160, 240, and 320 mg dose cohorts with10 participants in each dose cohort (8 participants received ZX-7101A tablets and 2 participants received placebo). The food effect (FE) part of the study was a randomised, 2-cycle, 2-way crossover design, which enrolled 16 participants to receive a single oral dose of 80 mg ZX-7101A tablets. Results: ZX-7101A tablets were safe and well-tolerated in both SAD and FE studies. No participant died or experienced SAE, or withdrew prematurely. The prodrug ZX-7101A was rapidly transformed into the active ingredient ZX-7101 after a single oral dose of 40-320 mg. The blood concentration of ZX-7101A was below the lower limit of quantification at most time points. ZX-7101 reached peak concentration about 3-4 h postdose in all dose cohorts. The elimination half-life of ZX-7101 was 83.01-125.55 h, and AUC 0-24 was 1655.4-11483.7 h*ng/mL. The FE part showed that the high-fat meal significantly affected the exposure parameters compared to the fasted condition. The C max and AUC0-t of ZX-7101 under the fasted condition were 1.73 and 1.78 times those under the fed condition, respectively. Conclusions: A single oral dose of 40 mg and 80 mg ZX-7101A tablets achieved sufficient ZX-7101 exposure for effectively inhibiting influenza A and B viruses and avian influenza viruses. These findings support 40 mg and 80 mg of ZX-7101A tablets as single dose regimens for use in phase II/III clinical trials. This study was registered at chinadrugtrials.org.cn (identifier: CTR20212778). (c) 2024 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页数:8
相关论文
共 17 条
[1]   Pharmacokinetic and pharmacodynamic analysis of baloxavir marboxil, a novel cap-dependent endonuclease inhibitor, in a murine model of influenza virus infection [J].
Ando, Yoshinori ;
Noshi, Takeshi ;
Sato, Kenji ;
Ishibashi, Toru ;
Yoshida, Yuki ;
Hasegawa, Takahiro ;
Onishi, Motoyasu ;
Kitano, Mitsutaka ;
Oka, Ryoko ;
Kawai, Makoto ;
Yoshida, Ryu ;
Sato, Akihiko ;
Shishido, Takao ;
Naito, Akira .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2021, 76 (01) :189-198
[2]  
[Anonymous], 2002, OIG-14431
[3]   Oseltamivir [J].
Bardsley-Elliot, A ;
Noble, S .
DRUGS, 1999, 58 (05) :851-860
[4]   Highly Pathogenic Avian Influenza H5N1 Virus Infections in Wild Red Foxes (Vulpes vulpes) Show Neurotropism and Adaptive Virus Mutations [J].
Bordes, Luca ;
Vreman, Sandra ;
Heutink, Rene ;
Roose, Marit ;
Venema, Sandra ;
Pritz-Verschuren, Sylvia B. E. ;
Rijks, Jolianne M. M. ;
Gonzales, Jose L. ;
Germeraad, Evelien A. A. ;
Engelsma, Marc ;
Beerens, Nancy .
MICROBIOLOGY SPECTRUM, 2023, 11 (01)
[5]   Highly Pathogenic Avian Influenza A(H5N1) Clade 2.3.4.4b Virus in Domestic Cat, France, 2022 [J].
Briand, Francois-Xavier ;
Souchaud, Florent ;
Pierre, Isabelle ;
Beven, Veronique ;
Hirchaud, Edouard ;
Herault, Fabrice ;
Planel, Rene ;
Rigaudeau, Angelina ;
Bernard-Stoecklin, Sibylle ;
Van der Werf, Sylvie ;
Lina, Bruno ;
Gerbier, Guillaume ;
Eterradossi, Nicolas ;
Schmitz, Audrey ;
Niqueux, Eric ;
Grasland, Beatrice .
EMERGING INFECTIOUS DISEASES, 2023, 29 (08) :1696-1698
[6]   Human seasonal influenza under COVID-19 and the potential consequences of influenza lineage elimination [J].
Dhanasekaran, Vijaykrishna ;
Sullivan, Sheena ;
Edwards, Kimberly M. ;
Xie, Ruopeng ;
Khvorov, Arseniy ;
Valkenburg, Sophie A. ;
Cowling, Benjamin J. ;
Barr, Ian G. .
NATURE COMMUNICATIONS, 2022, 13 (01)
[7]   Baloxavir Marboxil for Uncomplicated Influenza in Adults and Adolescents [J].
Hayden, Frederick G. ;
Sugaya, Norio ;
Hirotsu, Nobuo ;
Lee, Nelson ;
de Jong, Menno D. ;
Hurt, Aeron C. ;
Ishida, Tadashi ;
Sekino, Hisakuni ;
Yamada, Kota ;
Portsmouth, Simon ;
Kawaguchi, Keiko ;
Shishido, Takao ;
Arai, Masatsugu ;
Tsuchiya, Kenji ;
Uehara, Takeki ;
Watanabe, Akira .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (10) :913-923
[8]   Baloxavir: First Global Approval [J].
Heo, Young-A .
DRUGS, 2018, 78 (06) :693-697
[9]   Epidemiological and virological surveillance of influenza viruses in China during 2020-2021 [J].
Huang, Wei-juan ;
Cheng, Yan-hui ;
Tan, Min-ju ;
Liu, Jia ;
Li, Xi-yan ;
Zeng, Xiao-xu ;
Tang, Jing ;
Wei, He-jiang ;
Chen, Tao ;
Yang, Lei ;
Xie, Yi-ran ;
Yang, Jia-ying ;
Xiao, Ning ;
Wang, Da-yan .
INFECTIOUS DISEASES OF POVERTY, 2022, 11 (01)
[10]   Drug resistance in influenza A virus: the epidemiology and management [J].
Hussain, Mazhar ;
Galvin, Henry D. ;
Haw, Tatt Y. ;
Nutsford, Ashley N. ;
Husain, Matloob .
INFECTION AND DRUG RESISTANCE, 2017, 10 :121-134