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The Japanese Early-Stage Trial of High-Dose Methylcobalamin for Amyotrophic Lateral Sclerosis (JETALS): Protocol for a Randomized Controlled Trial

Authors :
Kazuyuki Noda
Hiroshi Nokihara
Kiyonobu Komai
Naoki Atsuta
Kazuto Nishinaka
Tatsuo Kagimura
Hiroaki Yanagawa
Jetals
Mitsuya Morita
Makiko Nagai
Tomohiko Ishihara
Takayoshi Shimohata
Yasutaka Sato
Makoto Urushitani
Yuishin Izumi
Yasuhiro Kojima
Masaya Oda
Shun Shimohama
Koji Abe
Toshio Shimizu
Hitoshi Kikuchi
Satoshi Kuwabara
Ryuji Kaji
Masahiro Sonoo
Hidefumi Ito
Sagiri Isose
Nobuo Kohara
Satoshi Teramukai
Hiroyuki Nodera
Ken Ikeda
Kensuke Noma
Ryosuke Oki
Daisuke Kuzume
Kazuaki Kanai
Source :
JMIR Research Protocols
Publication Year :
2018
Publisher :
JMIR Publications, 2018.

Abstract

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

Details

Language :
English
ISSN :
19290748
Volume :
7
Issue :
12
Database :
OpenAIRE
Journal :
JMIR Research Protocols
Accession number :
edsair.doi.dedup.....e6ad774e034eda62ab8e1082d68e9dfa