Cumulative major molecular response (MMR) rate of 69% by 24 weeks, with 53% of patients achieving MMR by 24 weeks in ongoing randomized Phase 1b cohorts
ELVN-001 continues to demonstrate a favorable safety and tolerability profile across all dose levels evaluated, consistent with previously reported data
Data further reinforce ELVN-001's positioning as the potentially best-in-class active-site TKI in CML
Multiple key data, regulatory and operational catalysts expected in 2026
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