The purpose of this study is to evaluate the safety, tolerability and determine the recommended dose for further clinical evaluation of ELVN-001 in patients with chronic myeloid leukemia with and without T315I mutations in patients who are relapsed, refractory or intolerant to TKIs.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Phase 1a: Incidence of dose limiting toxicities
Timeframe: 28 days
Phase 1a: Incidence of adverse events (AEs)
Timeframe: up to 28 days
Phase 1a: Incidence of clinically significant laboratory abnormalities
Timeframe: up to 28 days
Phase 1a: Incidence of clinically significant ECG abnormalities
Timeframe: up to 28 days
Phase 1b: Incidence of adverse events
Timeframe: up to 3 years
Phase 1b: Incidence of clinically significant laboratory abnormalities
Timeframe: up to 3 years
Phase 1b: Incidence of clinically significant ECG abnormalities
Timeframe: up to 3 years