Intellia Therapeutics and ReCode Therapeutics Enter into a Collaboration Agreement to Develop Novel Gene Editing Therapies for Cystic Fibrosis (CF)
Shots:
- The collaboration combines Intellia’s CRISPR-based gene editing platform incl. DNA writing technology with ReCode’s SORT LNP delivery platform to correct CF disease-causing gene mutations
- The companies will initially focus on developing therapies for CF patients with limited or no treatment options. As per the agreement, Intellia will design the editing strategy & research-grade components for the investigational therapies & ReCode will lead the subsequent pre/clinical development & commercialization of certain programs globally
- Intellia will be eligible to receive a pre-specified development & commercial milestone payment, plus royalties & is also eligible to exercise an option to lead commercialization across the US for certain programs
Ref: Intellia Therapeutics | Image: Intellia Therapeutics
Related News:- Vertex’s Kaftrio+Ivacafor Receives EC’s Approval for the Treatment of Children aged 2 to 5yrs. with Cystic Fibrosis (CF)
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Shivani was a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She was covering news related to Product approvals, clinical trial results, and updates. We can be contacted at connect@pharmashots.com.