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Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults
PURPOSE: Herpes zoster (HZ), or shingles, is a clinical syndrome resulting from the reactivation of latent varicella zoster virus (VZV) within the sensory ganglia. We evaluated the safety and tolerability of ES16001 (ethanol extract of Elaeocarpus sylvestris var. ellipticus), a novel inhibitor of va...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359576/ https://www.ncbi.nlm.nih.gov/pubmed/34384499 http://dx.doi.org/10.1186/s40001-021-00565-z |
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author | Hwang-Bo, Jeon Kim, Byungwook Park, Dae Won Lee, Yeong-Geun Kwon, Jeong Eun Chung, Jae-Yong Kang, Se Chan |
author_facet | Hwang-Bo, Jeon Kim, Byungwook Park, Dae Won Lee, Yeong-Geun Kwon, Jeong Eun Chung, Jae-Yong Kang, Se Chan |
author_sort | Hwang-Bo, Jeon |
collection | PubMed |
description | PURPOSE: Herpes zoster (HZ), or shingles, is a clinical syndrome resulting from the reactivation of latent varicella zoster virus (VZV) within the sensory ganglia. We evaluated the safety and tolerability of ES16001 (ethanol extract of Elaeocarpus sylvestris var. ellipticus), a novel inhibitor of varicella zoster virus reactivation in healthy adults. METHOD: Single-center, randomized, double-blind, placebo-controlled, single and multiple ascending dose (SAD and MAD, respectively) studies were conducted in 20- to 45-year-old healthy adults without chronic disease. In the SAD study (n = 32), subjects randomly received a single oral dose of 240, 480, 960, or 1440 mg ES16001 or a placebo. In the MAD study (n = 16), subjects randomly received once daily doses of 480 or 960 mg ES16001 or a placebo for 5 days. The safety and tolerability of the drug were evaluated by monitoring participants’ treatment emergent adverse events (TEAEs) and vital signs, electrocardiograms (ECGs), physical examinations, and clinical laboratory tests. RESULTS: In the SAD study, 11 adverse reactions were seen in 5 subjects, and in the MAD study, 8 adverse reactions were seen in 6 subjects. All adverse reactions were mild, and no serious adverse reactions occurred. The most common adverse reaction was an increase in alanine aminotransferase (ALT), but all test values were in the clinically non-significant range, and their clinical significance was judged to be small considering the fact that most of the test values returned to normal immediately after the end of drug administration. CONCLUSION: ES16001 has good safety and tolerability when administered both once and repeatedly to healthy subjects. Further research is needed to identify any possible drug-induced hepatotoxicity, which appears infrequently. Our findings provide a rationale for further clinical investigations of ES16001 for the prevention of HZ. Trial registration: CRIS, KCT0006066. Registered 7 April 2021—Retrospectively registered, https://cris.nih.go.kr/cris/search/detailSearch.do/19071). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-021-00565-z. |
format | Online Article Text |
id | pubmed-8359576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83595762021-08-16 Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults Hwang-Bo, Jeon Kim, Byungwook Park, Dae Won Lee, Yeong-Geun Kwon, Jeong Eun Chung, Jae-Yong Kang, Se Chan Eur J Med Res Research PURPOSE: Herpes zoster (HZ), or shingles, is a clinical syndrome resulting from the reactivation of latent varicella zoster virus (VZV) within the sensory ganglia. We evaluated the safety and tolerability of ES16001 (ethanol extract of Elaeocarpus sylvestris var. ellipticus), a novel inhibitor of varicella zoster virus reactivation in healthy adults. METHOD: Single-center, randomized, double-blind, placebo-controlled, single and multiple ascending dose (SAD and MAD, respectively) studies were conducted in 20- to 45-year-old healthy adults without chronic disease. In the SAD study (n = 32), subjects randomly received a single oral dose of 240, 480, 960, or 1440 mg ES16001 or a placebo. In the MAD study (n = 16), subjects randomly received once daily doses of 480 or 960 mg ES16001 or a placebo for 5 days. The safety and tolerability of the drug were evaluated by monitoring participants’ treatment emergent adverse events (TEAEs) and vital signs, electrocardiograms (ECGs), physical examinations, and clinical laboratory tests. RESULTS: In the SAD study, 11 adverse reactions were seen in 5 subjects, and in the MAD study, 8 adverse reactions were seen in 6 subjects. All adverse reactions were mild, and no serious adverse reactions occurred. The most common adverse reaction was an increase in alanine aminotransferase (ALT), but all test values were in the clinically non-significant range, and their clinical significance was judged to be small considering the fact that most of the test values returned to normal immediately after the end of drug administration. CONCLUSION: ES16001 has good safety and tolerability when administered both once and repeatedly to healthy subjects. Further research is needed to identify any possible drug-induced hepatotoxicity, which appears infrequently. Our findings provide a rationale for further clinical investigations of ES16001 for the prevention of HZ. Trial registration: CRIS, KCT0006066. Registered 7 April 2021—Retrospectively registered, https://cris.nih.go.kr/cris/search/detailSearch.do/19071). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-021-00565-z. BioMed Central 2021-08-12 /pmc/articles/PMC8359576/ /pubmed/34384499 http://dx.doi.org/10.1186/s40001-021-00565-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hwang-Bo, Jeon Kim, Byungwook Park, Dae Won Lee, Yeong-Geun Kwon, Jeong Eun Chung, Jae-Yong Kang, Se Chan Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
title | Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
title_full | Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
title_fullStr | Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
title_full_unstemmed | Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
title_short | Safety, tolerability of ES16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
title_sort | safety, tolerability of es16001, a novel varicella zoster virus reactivation inhibitor, in healthy adults |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359576/ https://www.ncbi.nlm.nih.gov/pubmed/34384499 http://dx.doi.org/10.1186/s40001-021-00565-z |
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