BridgeBio gears up for rare muscular dystrophy launch with FDA approval in sight

If approved, BridgeBio Pharma’s BBP-418—which, according to one Jefferies analyst, boasts “pretty darn compelling” data—would be the first therapy for limb-girdle muscular dystrophy. The FDA has an action date of Nov. 27.

Leave a Comment

Your email address will not be published. Required fields are marked *

Scroll to Top