
Cystic Fibrosis Foundation Invests $15M in ReCode for Gene Editing
Key Highlights
- Cystic Fibrosis Foundation commits $15M to ReCode Therapeutics for lung-targeted gene editing collaboration with Intellia Therapeutics.
- ReCode focuses on lipid nanoparticle delivery systems for lung stem cell targeting, critical for permanent gene correction.
- Intellia’s therapy aims to correct CFTR gene nonsense mutations affecting individuals not eligible for CFTR modulators.
- Investment builds on a separate $15M CF Foundation funding for messenger RNA therapy now in clinical trials.
- The initiative targets transformative treatments for CF, particularly for patients unable to benefit from current modulators.
Source: Business Wire
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