Clinical DataUpdated Phase 1b data for SL-172154 in combination with azacitidine in high-risk myelodysplastic syndromes and TP53-mutant acute myeloid leukemia showed improved and stable complete remission and overall response rates above most historical data.
FinancialsThe company ended the quarter with $117.2 million in cash, which management believes provides runway for all ongoing operations into 2026, beyond results from its Phase 1 clinical trials of SL-172154.
Regulatory EnvironmentWith the FDA showing growing comfort with minimal residual disease analyses, there is a possibility that this effect, if replicated in randomized cohorts, could ultimately form the basis of an accelerated approval.