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Pestronk, Alan

https://orcid.org/0000-0002-8991-5770

A5025781296 | I204465549

Mayo Clinic

Washington University in St. Louis

Citations 8

A randomized, double-blind, placebo-controlled study of losmapimod in patients with facioscapulohumeral muscular dystrophy: Results of the REACH study

Journal of Neuromuscular Diseases | February 6, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1177/22143602261419558 | PMID 41649965

Background: Losmapimod is an orally administered small molecule and selective p38α/β mitogen-activated protein kinase (MAPK) inhibitor able to reduce aberrant expression of DUX4 in vitro and thereby potentially slowing disease progression in patients with facioscapulohumeral muscular dystrophy (FSHD). Objective: This global, randomized, placebo-controlled, double-blind phase 3 study in patients with FSHD1 and FSHD2 examined the efficacy and safety of losmapimod over a 48-week treatment period compared to placebo (NCT05397470, EUDRACT 2022-000389-16). Methods: The primary endpoint was change in quantification of reachable workspace (RWS) expressed as relative surface area (RSA). Other endpoints included measures of muscle composition (fat content and lean muscle) using magnetic resonance imaging (MRI), muscle strength using quantitative dynamometry, and quality of life measures. Results: 130 participants received losmapimod and 130 participants received placebo, with 252 participants completing the 48-week treatment period. There were no statistically significant differences between groups in change in RSA and all secondary efficacy endpoints from baseline to Week 48. Losmapimod treatment was well-tolerated, and most adverse events were mild. Conclusions: Losmapimod was generally well tolerated with a favorable safety profile at a dose of 15 mg twice daily. Although none of the efficacy endpoints were met, study design and data from the study may inform future studies of FSHD therapies.
Dysferlinopathy as Cause of Long-term Asymptomatic HyperCKemia and Myalgia (P10-11.016)

Neurology | April 7, 2025 | Volume: 104 | Issue: 7_Supplement_1 | Pages: No page available

10.1212/wnl.0000000000210746

Ophthalmoparesis as an Unusual Manifestation of Anti-HMGCR Antibody-related Myopathies (P11-11.007)

Neurology | April 9, 2024 | Volume: 102 | Issue: 7_supplement_1 | Pages: No page available

10.1212/wnl.0000000000205413

Efficacy and Safety of Dichlorphenamide for the Treatment of Periodic Paralysis: a Phase 3 Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Trial (PL02.001)

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.pl02.001

Survival and Disease Progression in SOD1 Familial ALS in North America (P3.185)

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.p3.185

Pentoxifylline as a rescue treatment for DMD

Neurology | March 8, 2012 | Volume: 78 | Issue: 12 | Pages: 904-913

10.1212/wnl.0b013e31824c46be | PMID 22402864

Phase II screening trial of lithium carbonate in amyotrophic lateral sclerosis

Neurology | August 4, 2011 | Volume: 77 | Issue: 10 | Pages: 973-979

10.1212/wnl.0b013e31822dc7a5 | PMID 21813790

P3‐287: TDP‐43 A315T mutation in familial motor neuron disease

Alzheimer's & Dementia | July 24, 2008 | Volume: 4 | Issue: 4S_Part_18 | Pages: No page available

10.1016/j.jalz.2008.05.1855