Editas Medicine reported a net loss of $60.7 million, or $0.88 per share, for the fourth quarter of 2022. Collaboration and other research and development revenues decreased, while research and development expenses increased due to investments in the EDIT-301 program.
Parallel patient dosing commenced in the EDIT-301 RUBY trial for SCD.
Clinical update for RUBY trial expected by mid-2023, with plans to dose 20 total patients by year-end.
First patient dosing in EDIT-301 EDITHAL trial for TDT is on track for Q1 2023, with a clinical update expected by year-end.
Agreement reached to sell iNK cell franchise and out-license gene editing technologies to Shoreline Biosciences.
Editas Medicine is focused on advancing its EDIT-301 program for SCD and TDT, with key milestones expected in 2023. The company also aims to sharpen its focus, strengthen its technology, and expand business development efforts.