Stopped: This decision is based solely on internal company prioritization and resource allocation considerations. No patients have been enrolled or dosed in this study and no clinical data have been generated.
This is a Phase 1a/1b, multicenter study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and clinical activity of TER-1754 (a novel AKT1 inhibitor) in patients with HHT.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Phase 1a: Safety and Tolerability of TER-1754
Timeframe: up to 48 weeks
Phase 1a: Maximum Tolerated Dose (MTD) and/or Maximum Administrated Dose (MAD) of TER-1754
Timeframe: 28 days
Phase 1b - Evaluate the Change from baseline in epistaxis and symptom-related clinical activity scores at Week 24
Timeframe: 48 weeks