A Prospective, Multicenter, Randomized Phase II Study to Evaluate the Efficacy and Safety of Eculizu...
A Prospective, Multicenter, Randomized Phase II Study to Evaluate the Efficacy and Safety of Eculizumab in Patients with Guillain-Barré Syndrome (GBS): Protocol of Japanese Eculizumab Trial for GBS (JET-GBS)
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Author / Creator
Yamaguchi, Nobuko , Misawa, Sonoko , Sato, Yasunori , Nagashima, Kengo , Katayama, Kanako , Sekiguchi, Yukari , Iwai, Yuta , Amino, Hiroshi , Suichi, Tomoki , Yokota, Takanori , Nishida, Yoichiro , Kohara, Nobuo , Hirata, Koichi , Nishiyama, Kazutoshi , Yabe, Ichiro , Kaida, Ken-Ichi , Suzuki, Norihiro , Nodera, Hiroyuki , Tsuji, Shoji , Koike, Haruki , Kira, Jun-Ichi , Hanaoka, Hideki , Kusunoki, Susumu , Kuwabara, Satoshi and JET-GBS Group
Publisher
Canada: JMIR Publications
Journal title
Language
English
Formats
Publication information
Publisher
Canada: JMIR Publications
Subjects
More information
Scope and Contents
Contents
Guillain-Barré syndrome (GBS) is an immune-mediated neuropathy that causes acute flaccid paralysis. Immunoglobulin and plasma exchange are established treatments for GBS; however, a substantial number of patients, particularly those with severe disease, have poor recovery and residual deficits. Recent studies suggest that complement activation plays a pivotal role in GBS-associated axonal degeneration, and eculizumab is a humanized monoclonal antibody that specifically binds to complement component 5 and potently inhibits complement activation.
This clinical trial aims to evaluate the efficacy and safety of eculizumab, a humanized monoclonal antibody directed against complement component 5, for treatment of GBS.
The Japanese Eculizumab Trial for GBS (JET-GBS) is a prospective, multicenter, placebo-controlled, double-blind, randomized phase II study conducted at 13 tertiary neurology centers and is funded by the Japan Agency for Medical Research and Development. A total of 33 GBS patients unable to walk independently within 2 weeks from symptom onset (Hughes functional grade 3-5) were randomized at a 2:1 ratio to receive either intravenous eculizumab (900 mg/day) or placebo once weekly for 4 weeks, followed by 20 weeks of follow-up. The primary endpoint for efficacy is the proportion of patients who regain their ability to walk without aid at 4 weeks after the first dose of the study treatment, while primary safety outcomes are the incidence of adverse events and serious adverse events during the trial.
Enrollment for the trial began in August 2015. This trial is still ongoing. All participants have been enrolled, and follow-up will be completed in October 2016.
This study is the first to investigate the efficacy and safety of eculizumab for GBS. In case of a positive result, we will plan a phase III trial to investigate this issue in a larger number of patients.
UMIN Clinical Trials Registry UMIN 000018171; https:/upload.umin.ac.jp/cgi-open-bin/ctr/ctr.cgi?function= brows&action=brows&type=summary&language=J&recptno=R000020978 (Archived by WebCite at http://www.webcitation.org/ 6lTiG8ltG). Clinical Trials.gov NCT02493725; https://clinicaltrials.gov/ct2/show/NCT02493725 (Archived by WebCite at http://www.webcitation.org/6lVJZXKSL)....
Alternative Titles
Full title
A Prospective, Multicenter, Randomized Phase II Study to Evaluate the Efficacy and Safety of Eculizumab in Patients with Guillain-Barré Syndrome (GBS): Protocol of Japanese Eculizumab Trial for GBS (JET-GBS)
Authors, Artists and Contributors
Author / Creator
Misawa, Sonoko
Sato, Yasunori
Nagashima, Kengo
Katayama, Kanako
Sekiguchi, Yukari
Iwai, Yuta
Amino, Hiroshi
Suichi, Tomoki
Yokota, Takanori
Nishida, Yoichiro
Kohara, Nobuo
Hirata, Koichi
Nishiyama, Kazutoshi
Yabe, Ichiro
Kaida, Ken-Ichi
Suzuki, Norihiro
Nodera, Hiroyuki
Tsuji, Shoji
Koike, Haruki
Kira, Jun-Ichi
Hanaoka, Hideki
Kusunoki, Susumu
Kuwabara, Satoshi
JET-GBS Group
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5118582
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5118582
Other Identifiers
ISSN
1929-0748
E-ISSN
1929-0748
DOI
10.2196/resprot.6610