REGULATORY
15 Jan 2026
PARTNERSHIPS
13 Jan 2026
INNOVATION
9 Jan 2026
PARTNERSHIPS
16 Dec 2025

INNOVATION
12 Dec 2025
New trial results suggest gene editing could move from rare use to everyday medicine, pending regulators

INNOVATION
5 Jun 2025
Sector turns to next-generation delivery and risk controls as in vivo gene editing moves toward wider clinical use

PARTNERSHIPS
21 May 2025
CHOP, Penn, and Acuitas use lipid nanoparticles for rare genetic disorder, bypassing viral vectors for the first time in the US.

INSIGHTS
15 May 2025
Mammoth’s one-dose CRISPR delivery to muscle raises hopes for wider, safer genetic treatments.
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