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A randomized placebo-controlled phase 3 study of mesenchymal stem cells induced to secrete high levels of neurotrophic factors in amyotrophic lateral sclerosis.

Authors :
Cudkowicz ME
Lindborg SR
Goyal NA
Miller RG
Burford MJ
Berry JD
Nicholson KA
Mozaffar T
Katz JS
Jenkins LJ
Baloh RH
Lewis RA
Staff NP
Owegi MA
Berry DA
Gothelf Y
Levy YS
Aricha R
Kern RZ
Windebank AJ
Brown RH Jr
Source :
Muscle & nerve [Muscle Nerve] 2022 Mar; Vol. 65 (3), pp. 291-302. Date of Electronic Publication: 2022 Jan 05.
Publication Year :
2022

Abstract

Introduction/aims: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative illness with great unmet patient need. We aimed to evaluate whether mesenchymal stem cells induced to secrete high levels of neurotrophic factors (MSC-NTF), a novel autologous cell-therapy capable of targeting multiple pathways, could safely slow ALS disease progression.<br />Methods: This randomized, double-blind, placebo-controlled study enrolled ALS participants meeting revised El Escorial criteria, revised ALS Functional Rating Scale (ALSFRS-R) ≥25 (screening) and ≥3 ALSFRS-R points decline prior to randomization. Participants received three treatments of MSC-NTF or placebo intrathecally. The primary endpoint evaluated efficacy of MSC-NTF through a responder analysis and safety. A change in disease progression post-treatment of ≥1.25 points/mo defines a clinical response. A pre-specified analysis leveraged baseline ALSFRS-R of 35 as a subgroup threshold.<br />Results: Overall, MSC-NTF treatment was well tolerated; there were no safety concerns. Thirty-three percent of MSC-NTF and 28% of placebo participants met clinical response criteria at 28 wk (odds ratio [OR] = 1.33, P = .45); thus, the primary endpoint was not met. A pre-specified analysis of participants with baseline ALSFRS-R ≥ 35 (n = 58) showed a clinical response rate at 28 wk of 35% MSC-NTF and 16% placebo (OR = 2.6, P = .29). Significant improvements in cerebrospinal biomarkers of neuroinflammation, neurodegeneration, and neurotrophic factor support were observed with MSC-NTF, with placebo unchanged.<br />Discussion: The study did not reach statistical significance on the primary endpoint. However, a pre-specified subgroup suggests that MSC-NTF participants with less severe disease may have retained more function compared to placebo. Given the unmet patient need, the results of this trial warrant further investigation.<br /> (© 2021 BrainStorm Cell Therapeutics. Muscle & Nerve published by Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1097-4598
Volume :
65
Issue :
3
Database :
MEDLINE
Journal :
Muscle & nerve
Publication Type :
Academic Journal
Accession number :
34890069
Full Text :
https://doi.org/10.1002/mus.27472