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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 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

In the News


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

View All News

Recent Publications


ALSUntangled #80: ISRIB (Integrated stress response InhiBitor).

Journal Article Amyotroph Lateral Scler Frontotemporal Degener · November 2025 ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we assess ISRIB, a molecule that attenuates the integrated stress response (ISR). The ISR is an intracellular signaling network thro ... Full text Link to item Cite

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

Journal Article Amyotroph Lateral Scler Frontotemporal Degener · September 13, 2025 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
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Recent Grants


SEA-NOBI-ALS

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

Pridopine EAP 2 (Clinical Site Agreement)

ResearchPrincipal Investigator · Awarded by Massachusetts General Hospital · 2024 - 2027

An Intermediate Expanded Access Protocol (EAP) with CNM-Au8 for Amyotrophic Lateral Sclerosis

ResearchPrincipal Investigator · Awarded by Clene Nanomedicine Inc. · 2024 - 2026

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Education, Training & Certifications


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