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The Japanese Early-Stage Trial of High-Dose Methylcobalamin for Amyotrophic Lateral Sclerosis (JETALS): Protocol for a Randomized Controlled Trial.
Oki, Ryosuke; Izumi, Yuishin; Nodera, Hiroyuki; Sato, Yasutaka; Nokihara, Hiroshi; Kanai, Kazuaki; Sonoo, Masahiro; Urushitani, Makoto; Nishinaka, Kazuto; Atsuta, Naoki; Kohara, Nobuo; Shimizu, Toshio; Kikuchi, Hitoshi; Oda, Masaya; Ikeda, Ken; Nagai, Makiko; Komai, Kiyonobu; Kojima, Yasuhiro; Kuzume, Daisuke; Isose, Sagiri; Shimohama, Shun; Abe, Koji; Ito, Hidefumi; Noda, Kazuyuki; Ishihara, Tomohiko; Morita, Mitsuya; Shimohata, Takayoshi; Teramukai, Satoshi; Kagimura, Tatsuo; Noma, Kensuke; Yanagawa, Hiroaki; Kuwabara, Satoshi; Kaji, Ryuji.
Afiliação
  • Oki R; Department of Clinical Neuroscience, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
  • Izumi Y; Department of Clinical Neuroscience, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
  • Nodera H; Department of Clinical Neuroscience, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
  • Sato Y; Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Nokihara H; Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Kanai K; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
  • Sonoo M; Department of Neurology, Teikyo University School of Medicine, Tokyo, Japan.
  • Urushitani M; Department of Neurology, Shiga University of Medical Science, Otsu, Japan.
  • Nishinaka K; Department of Neurology, Sumitomo Hospital, Osaka, Japan.
  • Atsuta N; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kohara N; Department of Neurology, Kobe City Medical Centre General Hospital, Kobe, Japan.
  • Shimizu T; Department of Neurology, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan.
  • Kikuchi H; Department of Neurology, Murakami Karindo Hospital, Fukuoka, Japan.
  • Oda M; Department of Neurology, Vihara Hananosato Hospital, Miyoshi, Japan.
  • Ikeda K; Department of Neurology, Toho University Omori Medical Center, Tokyo, Japan.
  • Nagai M; Department of Neurology, Kitasato University East Hospital, Sagamihara, Japan.
  • Komai K; Department of Neurology, National Hospital Organization Iou Hospital, Kanazawa, Japan.
  • Kojima Y; Department of Neurology, Takeda General Hospital, Kyoto, Japan.
  • Kuzume D; Department of Neurology, Chikamori Hospital, Kochi, Japan.
  • Isose S; Department of Neurology, National Hospital Organization Chiba-East Hospital, Chiba, Japan.
  • Shimohama S; Department of Neurology, Sapporo Medical University, Sapporo, Japan.
  • Abe K; Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
  • Ito H; Department of Neurology, Wakayama Medical University, Wakayama, Japan.
  • Noda K; Department of Neurology, Juntendo University Shizuoka Hospital, Izunokuni, Japan.
  • Ishihara T; Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.
  • Morita M; Division of Neurology, Department of Internal Medicine, Jichi Medical University, Tochigi, Japan.
  • Shimohata T; Department of Neurology and Geriatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Teramukai S; Department of Biostatistics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Kagimura T; Translational Research Center for Medical Innovation, Foundation for Biomedical Research and Innovation, Kobe, Japan.
  • Noma K; Division of Regeneration and Medicine, Medical Center for Translational and Clinical Research, Hiroshima University Hospital, Hiroshima, Japan.
  • Yanagawa H; Department of Cardiovascular Regeneration and Medicine, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
  • Kuwabara S; Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Kaji R; Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.
JMIR Res Protoc ; 7(12): e12046, 2018 12 21.
Article em En | MEDLINE | ID: mdl-30578206
BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that affects the upper and lower motor neurons. Currently, only riluzole and edaravone are approved as drugs to treat ALS and new agents with larger effect sizes are warranted. Exploratory analyses in our previous study (study ID #E0302-J081-761) have suggested that high-dose methylcobalamin (E0302) prolonged the overall survival of ALS patients and suppressed ALS progression in patients with a disease duration of less than 12 months. OBJECTIVE: This clinical trial aims to evaluate the efficacy and safety of E0302 for treatment of ALS patients within one year of onset. METHODS: The Japanese early-stage trial of high-dose methylcobalamin for ALS (JETALS) is a prospective, multicenter, placebo-controlled, double-blind, randomized phase III study conducted at 24 tertiary neurology centers and is funded by the Japan Agency for Medical Research and Development. A total of 128 ALS patients within one year of onset were randomized at a 1:1 ratio to receive intramuscular injection with E0302 50 mg or placebo twice a week for 16 weeks. The primary endpoint is changes in the ALS Functional Rating Scale-Revised (ALSFRS-R) total score at 16 weeks. If patients wish to receive E0302 50 mg after the double-blind administration period, E0302 will be provided to them until March 2020 during the continuous administration period. RESULTS: This study began in October 2017 and is being conducted at 24 participating institutions in Japan. The study is in progress and the patient enrollment period is scheduled to end in August 2019, with follow-up scheduled to end in March 2020. CONCLUSIONS: This study is being performed to revalidate the efficacy and safety of E0302 in patients with early-stage ALS in the first year of symptom onset. If positive results are obtained, the aim is to apply for E0302 approval as a new drug for the treatment of ALS. TRIAL REGISTRATION: ClinicalTrials.gov NCT03548311; https://clinicaltrials.gov/ct2/show/NCT03548311 (Archived by WebCite at http://www.webcitation.org/74Fw3rDzb). INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/12046.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article