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Barry J Byrne, MD, PhD

Pediatric Cardiologist

Photo of Barry J Byrne

Research at a glance

Top areas of exploration

  • Genetic Therapy , 88 publications
  • Genetic Vectors , 80 publications
  • Glycogen Storage Disease Type II , 61 publications
  • Muscle, Skeletal , 42 publications

Research activity

361 publications

22,175 citations

Why is this important?

Active clinical trials

Solid - SGT - 001

This is a controlled, open-label, single-ascending dose study to evaluate the safety, tolerability and efficacy of SGT-001 in adolescents and children with Duchenne muscular dystrophy (DMD). Patients will receive a single intravenous (IV) infusion鈥�

Investigator
Barry J Byrne
Status
Accepting Candidates
Ages
4 Years - 17 Years
Sexes
Male

My publications

361 publications

2024

Neonatal systemic gene therapy restores cardiorespiratory function in a rat model of Pompe disease.

bioRxiv : the preprint server for biology

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2024

Neurological glycogen storage diseases and emerging therapeutics.

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics

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2024

Perspectives of the Friedreich ataxia community on gene therapy clinical trials.

Molecular therapy. Methods & clinical development

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2024

Safety and efficacy of givinostat in boys with Duchenne muscular dystrophy (EPIDYS): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.

The Lancet. Neurology

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2024

Switching treatment to cipaglucosidase alfa plus miglustat positively affects patient-reported outcome measures in patients with late-onset Pompe disease.

Journal of patient-reported outcomes

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