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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.
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.
Afiliação
  • Haji S; Department of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Fujita K; Department of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Oki R; Department of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Osaki Y; Department of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Miyamoto R; Department of Neurology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Morino H; Department of Medical Genetics, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Nagano S; Department of Neurotherapeutics, Osaka University Graduate School of Medicine, Suita, Japan.
  • Atsuta N; Department of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Kanazawa Y; Department of Neurology, Aichi Medical University School of Medicine, Nagakute, Japan.
  • Matsumoto Y; Department of Biomedical Information Sciences, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Arisawa A; Department of Radiology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Kawai H; Department of Diagnostic and Interventional Radiology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Sato Y; Department of Radiology, Aichi Medical University School of Medicine, Nagakute, Japan.
  • Sakaguchi S; Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Yagi K; Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Hamatani T; Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Kagimura T; Sumitomo Pharma Co, Ltd, Osaka, Japan.
  • Yanagawa H; The Translational Research Center for Medical Innovation, Foundation for Biomedical Research and Innovation at Kobe, Kobe, Japan.
  • Mochizuki H; Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Doyu M; Department of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Sobue G; Department of Neurology, Aichi Medical University School of Medicine, Nagakute, Japan.
  • Harada M; Aichi Medical University School of Medicine, Nagakute, Japan.
  • Izumi Y; Department of Radiology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
JMIR Res Protoc ; 12: e42032, 2023 Jan 30.
Article em En | MEDLINE | ID: mdl-36716091
ABSTRACT

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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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article