CUE-401 — Initial data
H2 2026
We anticipate receiving human safety data in the second half of 2026 and human proof-of-concept data in the second half of 2027.Source filing
catalyst calendar
CUE BIOPHARMA INC · Data as of 2026-10-25
H2 2026
We anticipate receiving human safety data in the second half of 2026 and human proof-of-concept data in the second half of 2027.Source filing
Late 2026
Company anticipates submitting an IND to the FDA and initiating a Phase 1 clinical study by year-end 2026Source filing
2027
Compelling data generated in preclinical models of multiple solid tumors, including pancreatic and ovarian, demonstrates the clinical potential of this novel immunotherapy approach with IND enabling studies on track for 2027 submissionSource filing
H2 2027
We anticipate receiving human safety data in the second half of 2026 and human proof-of-concept data in the second half of 2027.Source filing