COMPANY
Iterion Therapeutics
Preclinical studies have shown tegavivint inhibits β-catenin activity without overt toxicity, and has been shown to not be affected by CTNNB1 gain-of-function mutations typically found in cancer cells.2-3, 5-10 In parallel with the tegavivint program, Iterion has ongoing R&D programs investigating and developing 2nd generation TBL1 inhibitors. From company website Source · Oct 13, 2026
Timeline
Clinical trials (lead sponsor) 2
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT05797805 | A Study of Tegavivint (BC2059) in Patients With Advanced Hepatocellular Carcinoma | Phase 1/Phase 2 | Recruiting | Sep 13, 2023 | 2026-05 (estimated) |
| NCT03459469 | Phase I, Open-label, Non-randomized Study to Evaluate Safety of BC2059 | I | Completed | Jul 15, 2018 | May 1, 2022 (actual) |
NIH awards 1
- NIH award 1R41HL142357-01 FY2018: $299,974 awarded for that fiscal year; activity R41 (STTR); PI LARSON, JEFFREY LEROY; recipient as written: ITERION THERAPEUTICS INC. , HOUSTON, TX. Chronic intrapulmonary delivery o source ↗