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An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder, with its currently approved drugs, including riluzole and edaravone, showing limited therapeutic effects. Therefore, safe and effective drugs are urgently necessary. EPI-589 is an orally available, small-molecule,...

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Autores principales: Haji, Shotaro, Fujita, Koji, Oki, Ryosuke, Osaki, Yusuke, Miyamoto, Ryosuke, Morino, Hiroyuki, Nagano, Seiichi, Atsuta, Naoki, Kanazawa, Yuki, Matsumoto, Yuki, Arisawa, Atsuko, Kawai, Hisashi, Sato, Yasutaka, Sakaguchi, Satoshi, Yagi, Kenta, Hamatani, Tatsuto, Kagimura, Tatsuo, Yanagawa, Hiroaki, Mochizuki, Hideki, Doyu, Manabu, Sobue, Gen, Harada, Masafumi, Izumi, Yuishin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926342/
https://www.ncbi.nlm.nih.gov/pubmed/36716091
http://dx.doi.org/10.2196/42032
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author Haji, Shotaro
Fujita, Koji
Oki, Ryosuke
Osaki, Yusuke
Miyamoto, Ryosuke
Morino, Hiroyuki
Nagano, Seiichi
Atsuta, Naoki
Kanazawa, Yuki
Matsumoto, Yuki
Arisawa, Atsuko
Kawai, Hisashi
Sato, Yasutaka
Sakaguchi, Satoshi
Yagi, Kenta
Hamatani, Tatsuto
Kagimura, Tatsuo
Yanagawa, Hiroaki
Mochizuki, Hideki
Doyu, Manabu
Sobue, Gen
Harada, Masafumi
Izumi, Yuishin
author_facet Haji, Shotaro
Fujita, Koji
Oki, Ryosuke
Osaki, Yusuke
Miyamoto, Ryosuke
Morino, Hiroyuki
Nagano, Seiichi
Atsuta, Naoki
Kanazawa, Yuki
Matsumoto, Yuki
Arisawa, Atsuko
Kawai, Hisashi
Sato, Yasutaka
Sakaguchi, Satoshi
Yagi, Kenta
Hamatani, Tatsuto
Kagimura, Tatsuo
Yanagawa, Hiroaki
Mochizuki, Hideki
Doyu, Manabu
Sobue, Gen
Harada, Masafumi
Izumi, Yuishin
author_sort Haji, Shotaro
collection PubMed
description BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder, with its currently approved drugs, including riluzole and edaravone, showing limited therapeutic effects. Therefore, safe and effective drugs are urgently necessary. EPI-589 is an orally available, small-molecule, novel redox-active agent characterized by highly potent protective effects against oxidative stress with high blood-brain barrier permeability. Given the apparent oxidative stress and mitochondrial dysfunction involvement in the pathogenesis of ALS, EPI-589 may hold promise as a therapeutic agent. OBJECTIVE: This protocol aims to describe the design and rationale for the EPI-589 Early Phase 2 Investigator-Initiated Clinical Trial for ALS (EPIC-ALS). METHODS: EPIC-ALS is an explorative, open-labeled, single-arm trial that evaluates the safety and tolerability of EPI-589 in patients with ALS. This trial consists of 12-week run-in, 24-week treatment, and 4-week follow-up periods. Patients will receive 500 mg of EPI-589 3 times daily over the 24-week treatment period. Clinical assessments include the mean monthly change of Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised total score. The biomarkers are selected to analyze the effect on oxidative stress and neuronal damage. The plasma biomarkers are 8-hydroxy-2′-deoxyguanosine (8-OHdG), 3-nitrotyrosine (3-NT), neurofilament light chain (NfL), phosphorylated neurofilament heavy chain (pNfH), homocysteine, and creatinine. The cerebrospinal fluid biomarkers are 8-OHdG, 3-NT, NfL, pNfH, and ornithine. The magnetic resonance biomarkers are fractional anisotropy in the corticospinal tract and N-acetylaspartate in the primary motor area. RESULTS: This trial began data collection in September 2021 and is expected to be completed in October 2023. CONCLUSIONS: This study can provide useful data to understand the characteristics of EPI-589. TRIAL REGISTRATION: Japan Primary Registries Network jRCT2061210031; tinyurl.com/2p84emu6 INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/42032
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spelling pubmed-99263422023-02-15 An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study Haji, Shotaro Fujita, Koji Oki, Ryosuke Osaki, Yusuke Miyamoto, Ryosuke Morino, Hiroyuki Nagano, Seiichi Atsuta, Naoki Kanazawa, Yuki Matsumoto, Yuki Arisawa, Atsuko Kawai, Hisashi Sato, Yasutaka Sakaguchi, Satoshi Yagi, Kenta Hamatani, Tatsuto Kagimura, Tatsuo Yanagawa, Hiroaki Mochizuki, Hideki Doyu, Manabu Sobue, Gen Harada, Masafumi Izumi, Yuishin JMIR Res Protoc Protocol BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder, with its currently approved drugs, including riluzole and edaravone, showing limited therapeutic effects. Therefore, safe and effective drugs are urgently necessary. EPI-589 is an orally available, small-molecule, novel redox-active agent characterized by highly potent protective effects against oxidative stress with high blood-brain barrier permeability. Given the apparent oxidative stress and mitochondrial dysfunction involvement in the pathogenesis of ALS, EPI-589 may hold promise as a therapeutic agent. OBJECTIVE: This protocol aims to describe the design and rationale for the EPI-589 Early Phase 2 Investigator-Initiated Clinical Trial for ALS (EPIC-ALS). METHODS: EPIC-ALS is an explorative, open-labeled, single-arm trial that evaluates the safety and tolerability of EPI-589 in patients with ALS. This trial consists of 12-week run-in, 24-week treatment, and 4-week follow-up periods. Patients will receive 500 mg of EPI-589 3 times daily over the 24-week treatment period. Clinical assessments include the mean monthly change of Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised total score. The biomarkers are selected to analyze the effect on oxidative stress and neuronal damage. The plasma biomarkers are 8-hydroxy-2′-deoxyguanosine (8-OHdG), 3-nitrotyrosine (3-NT), neurofilament light chain (NfL), phosphorylated neurofilament heavy chain (pNfH), homocysteine, and creatinine. The cerebrospinal fluid biomarkers are 8-OHdG, 3-NT, NfL, pNfH, and ornithine. The magnetic resonance biomarkers are fractional anisotropy in the corticospinal tract and N-acetylaspartate in the primary motor area. RESULTS: This trial began data collection in September 2021 and is expected to be completed in October 2023. CONCLUSIONS: This study can provide useful data to understand the characteristics of EPI-589. TRIAL REGISTRATION: Japan Primary Registries Network jRCT2061210031; tinyurl.com/2p84emu6 INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/42032 JMIR Publications 2023-01-30 /pmc/articles/PMC9926342/ /pubmed/36716091 http://dx.doi.org/10.2196/42032 Text en ©Shotaro Haji, Koji Fujita, Ryosuke Oki, Yusuke Osaki, Ryosuke Miyamoto, Hiroyuki Morino, Seiichi Nagano, Naoki Atsuta, Yuki Kanazawa, Yuki Matsumoto, Atsuko Arisawa, Hisashi Kawai, Yasutaka Sato, Satoshi Sakaguchi, Kenta Yagi, Tatsuto Hamatani, Tatsuo Kagimura, Hiroaki Yanagawa, Hideki Mochizuki, Manabu Doyu, Gen Sobue, Masafumi Harada, Yuishin Izumi. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 30.01.2023. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on https://www.researchprotocols.org, as well as this copyright and license information must be included.
spellingShingle Protocol
Haji, Shotaro
Fujita, Koji
Oki, Ryosuke
Osaki, Yusuke
Miyamoto, Ryosuke
Morino, Hiroyuki
Nagano, Seiichi
Atsuta, Naoki
Kanazawa, Yuki
Matsumoto, Yuki
Arisawa, Atsuko
Kawai, Hisashi
Sato, Yasutaka
Sakaguchi, Satoshi
Yagi, Kenta
Hamatani, Tatsuto
Kagimura, Tatsuo
Yanagawa, Hiroaki
Mochizuki, Hideki
Doyu, Manabu
Sobue, Gen
Harada, Masafumi
Izumi, Yuishin
An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study
title An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study
title_full An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study
title_fullStr An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study
title_full_unstemmed An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study
title_short An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study
title_sort exploratory trial of epi-589 in amyotrophic lateral sclerosis (epic-als): protocol for a multicenter, open-labeled, 24-week, single-group study
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926342/
https://www.ncbi.nlm.nih.gov/pubmed/36716091
http://dx.doi.org/10.2196/42032
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