Editas Medicine gets approval to start Phase 1/2 EDIT-401 trial in Australia
The company plans patient dosing this year, reporting initial safety data in Q1 2027, while new preclinical durability data presents at the AHA Scientific Sessions.
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Gene editing company developing CRISPR medicines
editasmedicine.comLast updated
In short: Editas Medicine advanced EDIT-401 toward first-in-human trials while cutting 65% of its workforce in a strategy shift.
The company plans patient dosing this year, reporting initial safety data in Q1 2027, while new preclinical durability data presents at the AHA Scientific Sessions.
The board approved a grant of up to 950,000 shares at $3.03 per share as an inducement for his employment, vesting over four years.
Dr Ory leads clinical strategy and trials for the company genome editing programs across multiple therapeutic areas.
EDIT-401 is on track for CTN submission this month, with preclinical data showing ~90% LDL-C reduction; company raised $125M and extends cash runway into 2H 2028.
In studies on non-human primates, EDIT-401 reduced bad cholesterol and other harmful blood fats by around 90%.
The addition of Editas Medicine’s novel gene editing SLEEK technology, combined with the use of a high efficiency and high fidelity proprietary CRISPR enzyme, and...
Editas Medicine, Inc.(NasdaqGS:EDIT) added to Russell 2500 Growth Benchmark CI Jun. 29 Editas Medicine, Inc.(NasdaqGS:EDIT) added to Russell 2000 Growth Benchmark CI Jun. 29 Editas...
Editas Medicine (NASDAQ:EDIT) is preparing to begin a first-in-human study of EDIT-401, an in vivo CRISPR-edited medicine designed to lower LDL cholesterol in patients with...
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