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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...

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Autores principales: Hwang-Bo, Jeon, Kim, Byungwook, Park, Dae Won, Lee, Yeong-Geun, Kwon, Jeong Eun, Chung, Jae-Yong, Kang, Se Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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.
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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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