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Richard Stanley Bedlack

Stewart, Hughes and Wendt Distinguished Professor
Neurology, Neuromuscular Disease
Duke Box 3333, Durham, NC 27710
932 Morreene Rd ROOM234, Durham, NC

Overview


1. Investigator-initiated and multi-center clinical trials testing new treatments for amyotrophic lateral sclerosis and diabetic neuropathy.

2. Epidemiologic studies to better understand the causes and variability in prognosis of amyotrophic lateral sclerosis and diabetic neuropathy.

3. Basic science studies to develop novel biomarkers for amyotrophic lateral sclerosis.

Current Duke Appointments & Affiliations


Stewart, Hughes and Wendt Distinguished Professor · 2023 - Present Neurology, Neuromuscular Disease, Neurology
Professor of Neurology · 2018 - Present Neurology, Neuromuscular Disease, Neurology
Faculty Network Member of the Duke Institute for Brain Sciences · 2011 - Present Duke Institute for Brain Sciences, University Institutes and Centers
Associate of the Duke Initiative for Science & Society · 2017 - Present Duke Science & Society, University Initiatives & Academic Support Units

Recent News Items


Published July 31, 2024
Study Finds Genetic Variant Among People Who Experience a Rare Recovery from ALS
Published May 4, 2023
Duke Awards 44 Distinguished Professorships
Published July 11, 2022
Watch Duke Doctors Race Cars to Raise Money for ALS

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Recent Scholarly Works


ALSUntangled #82: N-acetylcysteine.

Journal article Amyotroph Lateral Scler Frontotemporal Degener · August 2026 N-acetylcysteine is a thiol-containing compound and a precursor of glutathione, with mechanistic plausibility for ALS, including reducing oxidative stress, regulating neuroinflammation, and mitigating mitochondrial dysfunction. Preclinical studies have yie ... Full text Link to item Cite

Examining IGFBP7 as a potential therapeutic target in people with ALS.

Journal article Amyotroph Lateral Scler Frontotemporal Degener · May 2026 A single nucleotide variant in an insulin-like growth factor (IGFBP7) promotor, which reduces IGFBP7 levels in brain, was previously associated with an ALS "reversal" phenotype. This raises the question of whether IGFBP7 might be a therapeutic target in AL ... Full text Link to item Cite

ALSUntangled #81: Pyridostigmine (mestinon®).

Journal article Amyotroph Lateral Scler Frontotemporal Degener · May 2026 Pyridostigmine (Mestinon®, Bausch Health, Canada Inc.) increases acetylcholine availability at the neuromuscular junction, enhancing transmission. Preclinical studies suggest that neuromuscular junction dysfunction develops early in ALS, and pyridostigmine ... Full text Link to item Cite
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Recent Grants


Healy ALS Platform Study - Regimen I - NUZ-001 TO#14

Clinical TrialPrincipal Investigator · Awarded by Massachusetts General Hospital · 2026 - 2030

SEA-NOBI-ALS

Clinical TrialPrincipal Investigator · Awarded by WideTrial, Inc. · 2025 - 2028

Clinical Research in ALS & Related Disorders for Therapeutic Development (CReATE)

ResearchPrincipal Investigator · Awarded by University of Miami · 2025 - 2027

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Education


University of Connecticut · 1995 Ph.D.
University of Connecticut · 1995 M.D.