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EP 126: Patient-led research for ultra-rare disease drug development with Julia Taravella, Executive Director of Rare Trait Hope Fund

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Manage episode 406430447 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
0:00 Introduction

0:25 Julia’s personal experience with ultra-rare diseases within her family

10:25 The importance of increasing accessibility to genetic testing across populations to learn more about ultra-rare diseases

14:00 The origin story of Rare Trait Hope Fund

23:50 Current research and next steps in developing potential gene therapies for aspartylglucosaminuria

32:20 How best to applykey insights and best practices to improve the approach to ultra-rare disease treatment development

38:30 Next steps for Rare Trait Hope Fund and how people can help with Julia’s mission

44:00 Julia’s advice for families who are advocating for rare disease research and therapy development

46:50 Closing remarks

For more information on Rare Trait Hope Fund, please visit: https://www.raretrait.com/.
  continue reading

169 episoade

Artwork
iconDistribuie
 
Manage episode 406430447 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
0:00 Introduction

0:25 Julia’s personal experience with ultra-rare diseases within her family

10:25 The importance of increasing accessibility to genetic testing across populations to learn more about ultra-rare diseases

14:00 The origin story of Rare Trait Hope Fund

23:50 Current research and next steps in developing potential gene therapies for aspartylglucosaminuria

32:20 How best to applykey insights and best practices to improve the approach to ultra-rare disease treatment development

38:30 Next steps for Rare Trait Hope Fund and how people can help with Julia’s mission

44:00 Julia’s advice for families who are advocating for rare disease research and therapy development

46:50 Closing remarks

For more information on Rare Trait Hope Fund, please visit: https://www.raretrait.com/.
  continue reading

169 episoade

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