Tier 2 — strong

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

de la Rubia JE, Drehmer E, Platero JL, Benlloch M, Caplliure-Llopis J, Villaron-Casales C, de Bernardo N, AlarcÓn J, Fuente C, Carrera S, Sancho D, GarcÍa-Pardo P, Pascual R, JuÁrez M, Cuerda-Ballester M, Forner A, Sancho-Castillo S, Barrios C, Obrador E, Marchio P, Salvador R, Holmes HE, Dellinger RW, Guarente L, Estrela JM
Amyotrophic lateral sclerosis & frontotemporal degeneration 2019 20; 1-2; 115-122

Bibliography

PubMed
PMID 30668199
Funding
Funding details are not specified in the accessible publication information.
Competing interests
A complete competing-interest declaration is not specified in the accessible publication information.

Study snapshot

DesignRandomized controlled study of a multi-ingredient or combined intervention
ModelHuman participants
Sample32 people with ALS recruited; 20 completed
InterventionEH301: NR plus pterostilbene versus placebo
Duration4 months
EndpointsALS functional rating; respiratory function; strength

What the study showed, in plain terms

This small EH301 pilot reported favorable functional, respiratory and strength measures compared with placebo.

Key findings

This small EH301 pilot reported favorable functional, respiratory and strength measures compared with placebo.

What this study can and cannot tell us

Substantial attrition, baseline imbalance concerns and combination treatment. The study does not establish NR monotherapy or confirmed disease modification.

Editorial review

Reviewed by the Biohack Blueprint research team

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