Clinical TrialsThe Phase 3 SELECT-MDS-1 study successfully passed a predetermined interim futility analysis regarding the complete response rate, conducted by an Independent Data Monitoring Committee.
Financial PerformanceFinancial results were largely consistent with consensus estimates, and Syros ended the quarter with $79MM in cash and reiterated guidance for runway into 3Q25.
Regulatory ApprovalsThe FDA recently granted Fast Track Designation to tamibarotene in combination with venetoclax and azacitidine.