Ernexa expects FDA review of ERNA-101 IND in Q4 2026

Eterna Therapeutics

Eterna Therapeutics

ERNA

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  • Ernexa set a Q3 2026 IND submission for ERNA-101, positioning the cell therapy for U.S. regulatory review.
  • The company targets FDA review in Q4 2026, with a first-in-human Phase 1 study planned to start in the same quarter.


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