Acrivon Announces Late-Breaking Oral Plenary Presentation of Early Phase 1/2 Clinical Results in AP3-Predicted Tumors for its First-in-Class WEE1/PKMYT1 Inhibitor ACR-2316 at the 38th EORTC-NCI-AACR Symposium
Acrivon said early Phase 1/2 dose-escalation results for ACR-2316 will be presented in a late-breaking oral plenary at the 38th EORTC-NCI-AACR Symposium on November 20, 2026. The company reported confirmed complete and partial responses in heavily pretreated AP3-predicted tumors, activity in K-Ras pathway-mutated cancers, and a favorable safety profile to date.
Why it matters — The reported clinical activity and safety findings, along with plans to expand the study to pancreatic cancer and explore combinations, are relevant to observers tracking ACRV’s ACR-2316 program.