Safety and efficacy of amnion-derived mesenchymal stem cells (AM01) in patients with steroid-refractory acute graft-versus-host disease after allogeneic haematopoietic stem cell transplantation: a study protocol for a phase I/II Japanese trial. Issue 7 (9th July 2019)

• Record Type: Journal Article
• Authors: Yamahara, Kenichi; Hamada, Akiko; Soma, Toshihiro; Okamoto, Rika; Okada, Masaya; Yoshihara, Satoshi; Yoshihara, Kyoko; Ikegame, Kazuhiro; Tamaki, Hiroya; Kaida, Katsuji; Inoue, Takayuki; Ohsugi, Yuko; Nishikawa, Hiroki; Hayashi, Hiroshi; Ito, Yoichi M; Iijima, Hiroaki; Ohnishi, Shunsuke; Hashimoto, Daigo; Isoe, Toshiyuki; Teshima, Takanori; Ogawa, Hiroyasu; Sato, Norihiro; Fujimori, Yoshihiro
• Is Part Of: BMJ open. Volume 9:Issue 7(2019)
• Publication Date: 2019-07-09
• Subjects: clinical trials -- haematology; Medicine -- Research -- Periodicals; 610.72
• DOI: 10.1136/bmjopen-2018-026403
• Languages: English
• ISSNs: 2044-6055

Abstract

Abstract : Introduction: Regenerative medicine and cell therapies have been gaining much attention among clinicians. Therapeutic infusion of mesenchymal stromal cells (MSCs) is now a leading investigational strategy for the treatment of acute graft-versus-host disease (aGVHD). Bone marrow MSCs are approved for manufacture and marketing as a cell therapy for aGVHD. Our non-clinical studies confirmed that human amnion-derived MSCs had immunomodulatory activity equal to or higher than that of human bone marrow MSCs. This study will aim to evaluate the safety and efficacy of amnion-derived MSCs (AM01) in patients with steroid-refractory aGVHD. Methods and analysis: This study will be a multicentre, single-arm, open-label trial (an interventional study). This clinical trial will begin with a low-dose group, and when safety has been confirmed in at least three cases in the low-dose group, treatment will begin for the high-dose group, for which the safety will also be verified. The primary endpoint is to assess the safety of intravenous infusion therapy of AM01 within 24 hours after intravenous infusion of AM01. The secondary endpoint is to explore the efficacy of intravenous infusion therapy with AM01. Ethics and dissemination: The institutional review boards of all participating hospitals approved this study protocol (latest V3.3.0, 3 August 2018). Final data will be publicly announced. A report releasing the study results will be submitted for publication to an appropriate peer-reviewed journal. Trial registration number: UMIN000029945.