other material
confidence high
sentiment positive
materiality 0.65
Lexeo Therapeutics licenses full data and IP for LX2006 FA cardiomyopathy gene therapy from Cornell
Lexeo Therapeutics, Inc.
- Upfront fees total $600,000; potential regulatory milestones up to $2.1M and commercial milestones up to $100M.
- Exclusive license to patent rights and non-exclusive know-how for AAVrh.10hFXN (LX2006), including right to reference IND.
- 11 participants dosed across two trials (Lexeo's SUNRISE-FA and Weill Cornell Phase 1A); no treatment-related SAEs reported.
- Interim clinical data readout expected mid-2024, combining data from both studies with up to 18-month follow-up.
- LX2006 has FDA Orphan Drug, Rare Pediatric Disease, and Fast Track designations for FA cardiomyopathy.