A phase Ib/IIa clinical trial of dantrolene sodium in patients with Wolfram syndrome

Damien Abreu1,2, Stephen I Stone3, Toni S Pearson4

  • 1Division of Endocrinology, Metabolism, and Lipid Research, Department of Medicine.

JCI Insight
|June 29, 2021
PubMed

Insights

Dantrolene sodium shows promise for Wolfram syndrome treatment, demonstrating good tolerability in patients. While not significantly improving all functions, it warrants further research for ER-targeted therapies.

Area of Science:

  • Rare genetic disorders
  • Endoplasmic reticulum (ER) stress
  • Neurodegenerative diseases

Background:

  • Wolfram syndrome is a rare ER disorder causing diabetes, optic nerve atrophy, and neurodegeneration.
  • Current treatments are lacking, but preclinical data suggest targeting ER calcium homeostasis may be beneficial.
  • Dantrolene sodium is a potential therapeutic agent for Wolfram syndrome.

Purpose of the Study:

  • To assess the safety and tolerability of dantrolene sodium in Wolfram syndrome patients.
  • To evaluate the efficacy of dantrolene sodium on pancreatic beta cell function, vision, and neurological functions.

Main Methods:

  • An open-label phase Ib/IIa clinical trial was conducted.
  • Adult and pediatric patients with Wolfram syndrome participated.
  • Safety, tolerability, and efficacy endpoints were measured over 6 months.

Main Results:

  • Dantrolene sodium was well-tolerated by all participants.
  • No significant improvement in overall beta cell function was observed.
  • A correlation was found between baseline beta cell function and responsiveness after treatment.

Conclusions:

  • Dantrolene sodium is safe and tolerable for Wolfram syndrome patients.
  • Further investigation into ER-targeting small molecules, including dantrolene sodium, is justified.
  • This study supports continued research for novel Wolfram syndrome treatments.