Biomarker & Efficacy ValidationAcrivon has developed an OncoSignature assay that successfully stratifies likely responders, enriching the objective response rate to 47%-58% compared to lower rates in previous studies.
Clinical Trials & Drug DevelopmentAcrivon's dual WEE1/PKMYT1 inhibitor, ACR-2316, has dosed the first patient ahead of schedule in its Phase 1 trial and completed the enrollment of the first cohort.
Financial PositionThe company has a strong cash position with $202.8M on the balance sheet, which is expected to support its operations until the second half of 2026.