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Intellia jumps as FDA lifts hold on gene‑editing trial for rare nerve disease

** Shares of gene therapy developer Intellia Therapeutics NTLA.O rise 21% to $16.87 premarket

** Co says U.S. FDA has lifted clinical hold on its late‑stage trial testing nex‑z for hereditary ATTR amyloidosis with polyneuropathy — a disease caused by harmful protein deposits that damage nerves

** FDA paused the study in October after a related‑trial patient had serious liver issues; Co agrees to tighter liver‑function monitoring - NTLA

** Co says it will raise trial size to about 60 patients from 50 and restart enrollment quickly

** Nex‑z is a one‑time therapy that co is developing with drugmaker Regeneron REGN.O, per co

** Shares down ~23% in 2025

 (Reporting by Sahil Pandey in Bengaluru)

 ((Sahil.Pandey@thomsonreuters.com))

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