SpliSense Secures Up to $13 Million from the Cystic Fibrosis Foundation to Advance Phase 2b Study of SPL84 for Cystic Fibrosis
Cystic Fibrosis Foundation funding follows positive SPL84 Phase 2a clinical results demonstrating clinical proof-of-concept for an inhaled antisense oligonucleotide therapy in a lung disease. Funding supports the ongoing global Phase 2b study evaluating SPL84 in people with cystic fibrosis carrying the 3849+10kb C-to-T mutation.
















































