Efficacy and tolerability of EH301 for amyotrophic lateral sclerosis: a randomized, double-blind, placebo-controlled human pilot study.

Raquel Pascual, José M Estrela, Leonard Guarente, Ryan W Dellinger, Holly E Holmes, Rosario Salvador, Patricia Marchio, Elena Obrador, Carlos Barrios, Sandra Sancho-Castillo, Alfonso Forner, María Cuerda-Ballester, Marta JuÁrez, JosÉ E de la Rubia, Pilar GarcÍa-Pardo, David Sancho, Sandra Carrera, Cristian Fuente, Jorge AlarcÓn, Nieves de Bernardo, Carlos Villaron-Casales, Jordi Caplliure-Llopis, MarÍa Benlloch, JosÉ L Platero, Eraci Drehmer

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration 2020;20(1-2):115-122

PMID: 30668199

Abstract

BACKGROUND

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease, characterized by progressive loss of spinal and cortical motor neurons, leading to muscular atrophy, respiratory failure, and ultimately death. There is no known cure, and the clinical benefit of the two drugs approved to treat ALS remains unclear. Novel disease-modifying therapeutics that are able to modulate the disease course are desperately needed. Our objective was to evaluate the efficacy and tolerability of Elysium Health's candidate drug EH301 in people with ALS (PALS).

METHODS

This was a single-center, prospective, double-blind, randomized, placebo-controlled pilot study. Thirty-two PALS were recruited thanks to the collaboration of the Spanish Foundation for ALS Research (FUNDELA). Study participants were randomized to receive either EH301 or placebo and underwent evaluation for 4 months. Differences between EH301 and placebo-treated participants were evaluated based on standard clinical endpoints, including the revised ALS functional rating scale (ALSFRS-R), forced vital capacity (FVC), and the Medical Research Council (MRC) grading scale.

RESULTS

Compared to placebo, participants treated with EH301 demonstrated significant improvements in the ALSFRS-R score, pulmonary function, muscular strength, and in skeletal muscle/fat weight ratio. EH301 was shown to significantly slow the progression of ALS relative to placebo, and even showed improvements in several key outcome measures compared with baseline.

CONCLUSIONS

This study provides evidence in support of the disease-modifying effects of EH301 for the treatment of ALS.

Address: a Department of Nursing , Catholic University San Vicente Mártir , Valencia , Spain.; b Department of Health and Functional Valorization , Catholic University San Vicente Martir , Valencia , Spain.; c Primary Care Service, University Hospital La Ribera , Alcira , Spain.; d Department of Physiotherapy , European University of Valencia , Valencia , Spain.; e Department of Health Sciences , Catholic University San Vicente Martir , Valencia , Spain.; f Department of Medicine , University Jaume I , Castellón , Spain.; g Rehabilitation Service, General University Hospital , Valencia , Spain.; h Clínica Artes & Timefit , Valencia , Spain.; i Institute for Research on Musculoskeletal Disorders , Catholic University San Vicente Mártir , Valencia , Spain.; j Department of Physiology , University of Valencia , Valencia , Spain.; k Virgen del Consuelo Hospital , Valencia , Spain.; l Elysium Health, Inc. , New York , NY , USA and.; m Department of Biology and Glenn Laboratories for the Science of Aging , MIT , Cambridge , MA , USA.
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