DiscoverCell & Gene: The PodcastIdentifying Drug Development Opportunities for DMD with CureDuchenne
Identifying Drug Development Opportunities for DMD with CureDuchenne

Identifying Drug Development Opportunities for DMD with CureDuchenne

Update: 2024-08-01
Share

Description

We love to hear from our listeners. Send us a message.

Debra Miller, CEO and Founder and Dr. Michael Kelly, Chief Scientific Officer at CureDuchenne talk to Host Erin Harris about the FDA approval for the expansion to the label indication for ELEVIDYS from Sarepta Therapeutics as well as how CureDuchenne works with various biotechs developing gene therapies for Duchenne muscular dystrophy (DMD). Miller and Kelly also share their advice and recommendations for companies developing drugs for DMD - while much progress has been made, more innovation is needed.

Subscribe to the podcast!
Apple | Spotify | YouTube

Comments 
In Channel
loading
00:00
00:00
x

0.5x

0.8x

1.0x

1.25x

1.5x

2.0x

3.0x

Sleep Timer

Off

End of Episode

5 Minutes

10 Minutes

15 Minutes

30 Minutes

45 Minutes

60 Minutes

120 Minutes

Identifying Drug Development Opportunities for DMD with CureDuchenne

Identifying Drug Development Opportunities for DMD with CureDuchenne

Erin Harris