Literature DB >> 35404074

Safety, Tolerability, and Pharmacokinetics of the Novel Hepatitis B Virus Expression Inhibitor GST-HG131 in Healthy Chinese Subjects: a First-in-Human Single- and Multiple-Dose Escalation Trial.

Xiaojiao Li1, Yusi Liu1, Hanxin Yao2, Meng Wang1, Lei Gao1, Jinfeng Lou1, John Mao3, Wenqiang Wu3, Yixin Zhou3, Yanan Tang3, Wenhao Yan3, Yanbin Hu4, Charles Ding5, Shuhui Chen5, Junqi Niu6, Yanhua Ding1.   

Abstract

GST-HG131, a novel dihydroquinolizinone (DHQ) compound, has been shown to reduce circulating levels of HBsAg in animals. This first-in-human trial evaluated the safety, tolerability, and pharmacokinetic profile of GST-HG131 in healthy Chinese subjects. This was a double-blind, randomized, placebo-controlled phase Ia clinical trial that was conducted in two parts. Part A was a single-ascending-dose (SAD; GST-HG131 10 30, 60, 100, 150, 200, 250 or 300 mg or placebo) study, which also assessed the food effect of GST-HG131 100 mg. Part B was a multiple-ascending-dose (MAD; GST-HG131 30, 60 or 100 mg or placebo BID) study. Tolerability assessments included adverse events, vital signs, 12-lead electrocardiogram, physical examination, and clinical laboratory tests. PK analyses were conducted in blood, urine, and fecal samples. Single doses of GST-HG131 ≤ 300 mg and multiple doses of GST-HG131 ≤ 60 mg were generally safe and well tolerated; however, multiple dosing was stopped at GST-HG131 100 mg, as pre-defined stopping rules specified in the protocol were met (Grade II drug related AEs of nausea and dizziness in >50% of subjects). In the SAD study, median tmax of GST-HG131 was 1-6 h, and t1/2 ranged from 3.88 h to 14.3 h. PK parameters were proportional to dose. Exposure was reduced after food intake. In the MAD study, steady-state was attained on day 4, and there was no apparent plasma accumulation of GST-HG131 on day 7 (Racc < 1.5). In conclusion, GST-HG131 exhibited an acceptable safety profile in healthy subjects at single doses ranging from 10-300 mg and multiple doses (BID) ranging from 30-60 mg, and the MAD doses (30 mg and 60 mg BID) that potentially meet the therapeutic AUC requirements. These findings imply GST-HG131 has potential as a therapeutic option for CHB infection. (This study has been registered at ClinicalTrials.gov under identifier NCT04499443.).

Entities:  

Keywords:  GST-HG131; food effect; hepatitis B virus expression inhibitor; pharmacokinetics; safety

Mesh:

Year:  2022        PMID: 35404074      PMCID: PMC9112976          DOI: 10.1128/aac.00094-22

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.938


  13 in total

1.  Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells.

Authors:  Neha Nagpal; Jianing Wang; Jing Zeng; Emily Lo; Diane H Moon; Kevin Luk; Roman O Braun; Lauri M Burroughs; Sioban B Keel; Christopher Reilly; R Coleman Lindsley; Scot A Wolfe; Albert K Tai; Patrick Cahan; Daniel E Bauer; Yick W Fong; Suneet Agarwal
Journal:  Cell Stem Cell       Date:  2020-04-21       Impact factor: 24.633

Review 2.  Therapeutic strategies for hepatitis B virus infection: towards a cure.

Authors:  Gregory C Fanning; Fabien Zoulim; Jinlin Hou; Antonio Bertoletti
Journal:  Nat Rev Drug Discov       Date:  2019-08-27       Impact factor: 84.694

3.  Discovery of RG7834: The First-in-Class Selective and Orally Available Small Molecule Hepatitis B Virus Expression Inhibitor with Novel Mechanism of Action.

Authors:  Xingchun Han; Chengang Zhou; Min Jiang; Yongguang Wang; Jianhua Wang; Zhanling Cheng; Min Wang; Yongqiang Liu; Chungen Liang; Jianping Wang; Zhanguo Wang; Robert Weikert; Wenzhe Lv; Jianxun Xie; Xin Yu; Xue Zhou; Souphalone Luangsay; Hong C Shen; Alexander V Mayweg; Hassan Javanbakht; Song Yang
Journal:  J Med Chem       Date:  2018-10-17       Impact factor: 7.446

4.  The Dihydroquinolizinone Compound RG7834 Inhibits the Polyadenylase Function of PAPD5 and PAPD7 and Accelerates the Degradation of Matured Hepatitis B Virus Surface Protein mRNA.

Authors:  Liren Sun; Fang Zhang; Fang Guo; Fei Liu; Jessie Kulsuptrakul; Andreas Puschnik; Min Gao; Rene Rijnbrand; Michael Sofia; Timothy Block; Tianlun Zhou
Journal:  Antimicrob Agents Chemother       Date:  2020-12-16       Impact factor: 5.191

5.  A novel orally available small molecule that inhibits hepatitis B virus expression.

Authors:  Henrik Mueller; Steffen Wildum; Souphalone Luangsay; Johanna Walther; Anaïs Lopez; Philipp Tropberger; Giorgio Ottaviani; Wenzhe Lu; Neil John Parrott; Jitao David Zhang; Roland Schmucki; Tomas Racek; Jean-Christophe Hoflack; Erich Kueng; Floriane Point; Xue Zhou; Guido Steiner; Marc Lütgehetmann; Gianna Rapp; Tassilo Volz; Maura Dandri; Song Yang; John A T Young; Hassan Javanbakht
Journal:  J Hepatol       Date:  2017-10-25       Impact factor: 25.083

6.  PAPD5/7 Are Host Factors That Are Required for Hepatitis B Virus RNA Stabilization.

Authors:  Henrik Mueller; Anaïs Lopez; Philipp Tropberger; Steffen Wildum; Josephine Schmaler; Lykke Pedersen; Xingchun Han; Yongguang Wang; Søren Ottosen; Song Yang; John A T Young; Hassan Javanbakht
Journal:  Hepatology       Date:  2019-03-01       Impact factor: 17.425

Review 7.  Toward a new era of hepatitis B virus therapeutics: The pursuit of a functional cure.

Authors:  Efthymios P Tsounis; Evanthia Tourkochristou; Athanasia Mouzaki; Christos Triantos
Journal:  World J Gastroenterol       Date:  2021-06-07       Impact factor: 5.742

8.  Efficacy of an Inhibitor of Hepatitis B Virus Expression in Combination With Entecavir and Interferon-α in Woodchucks Chronically Infected With Woodchuck Hepatitis Virus.

Authors:  Stephan Menne; Steffen Wildum; Guido Steiner; Manasa Suresh; Kyle Korolowicz; Maria Balarezo; Changsuek Yon; Marta Murreddu; Xupeng Hong; Bhaskar V Kallakury; Robin Tucker; Song Yang; John A T Young; Hassan Javanbakht
Journal:  Hepatol Commun       Date:  2020-04-22

Review 9.  Hepatitis B Virus Cure: Targets and Future Therapies.

Authors:  Hye Won Lee; Jae Seung Lee; Sang Hoon Ahn
Journal:  Int J Mol Sci       Date:  2020-12-28       Impact factor: 5.923

10.  Hepatoselective Dihydroquinolizinone Bis-acids for HBsAg mRNA Degradation.

Authors:  Nicky Hwang; Liren Sun; Daisy Noe; Patrick Y S Lam; Tianlun Zhou; Timothy M Block; Yanming Du
Journal:  ACS Med Chem Lett       Date:  2021-06-22       Impact factor: 4.632

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