Home
Categories
EXPLORE
Music
Education
Technology
History
Science
News
Society & Culture
About Us
Contact Us
Copyright
© 2024 PodJoint
00:00 / 00:00
Sign in

or

Don't have an account?
Sign up
Forgot password
https://is1-ssl.mzstatic.com/image/thumb/Podcasts125/v4/4d/06/80/4d068008-4092-58f8-6592-f900e2d86508/mza_5090466875224206838.jpeg/600x600bb.jpg
RARECast
RARECast
570 episodes
6 days ago

RARECast is a Global Genes podcast hosted by award-winning journalist Daniel Levine. It focuses on the intersection of rare disease with business, science, and policy.

Show more...
Business
RSS
All content for RARECast is the property of RARECast and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.

RARECast is a Global Genes podcast hosted by award-winning journalist Daniel Levine. It focuses on the intersection of rare disease with business, science, and policy.

Show more...
Business
https://content.production.cdn.art19.com/images/78/62/a0/61/7862a061-1aa5-444e-930f-1ae380f2243f/2d4db572ece3b5f6f2226f0fd6a05549552ced99839225e9ca281c4efc9f05c4d01c0bd056920ee48155e9ac30d73d97d96d460f45cd0dd760e9a62efea54909.jpeg
Changing a Treatment Landscape by De-Risking Drug Development
RARECast
28 minutes 8 seconds
2 weeks ago
Changing a Treatment Landscape by De-Risking Drug Development
Spinocerebellar ataxia is a group of inherited, heterogeneous neurodegenerative diseases affecting coordination, speech, and vision. There are currently no FDA approved therapies for the more than 50 known types of SCA​, but there is a growing pipeline of therapeutic candidates. We spoke to Andrew Rosen, CEO of the National Ataxia Foundation, about the challenges of developing therapies for spinocerebellar ataxia, the critical role of patient-led organizations in early-stage research and advocacy, and the recent surge of therapeutic activity targeting these neurodegenerative conditions.
RARECast

RARECast is a Global Genes podcast hosted by award-winning journalist Daniel Levine. It focuses on the intersection of rare disease with business, science, and policy.