Biopharma Transcript

Acrivon Therapeutics, Inc. ACRV

Nasdaq · Phase 2 · oncology · small molecule · EDGAR · Updated Oct 24, 2026

Acrivon Therapeutics, Inc. (Nasdaq: ACRV) is an oncology drug developer. Its lead program, ACR-368 (prexasertib), is in Phase 2 for endometrial cancer.

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
ACR-368endometrial cancersmall moleculePhase 2
ACR-2316solid tumors (WEE1/PKMYT1)small moleculePhase 1
CDK11 programoncologysmall moleculePre-clinical

Recent results and decisions

  1. Aug 12, 2026
    started ACR-2316 advanced into randomized dose expansion (120 mg and 160 mg QD, 3d on/4d off) of the Phase 1/2 study.ACR-2316 advanced into the randomized dose expansion stage of the Phase 1/2 study, supported by observed favorable safety profile and durable antitumor activity. Filing
  2. May 13, 2026
    started Arm 4 (single-agent ACR-368, all-comer serous EC) enrollment and dosing recently initiated.Arm 4 enrollment and dosing was recently initiated, investigating single agent ACR-368 without ULDG, in the same “serous all comer” subject population as Arm 3 Filing
  3. Mar 19, 2026
    positive ESGO late-breaker recap: serous EC cORR 52% (N=23) vs 22% (N=37) non-serous in subjects with <=2 prior lines (previously reported in Jan 2026).Consistent with higher BM levels in serous versus non-serous EC, an interim analysis across both OncoSignature-positive (BM+) and BM- serous EC subjects showed a cORR of 52% (N = 23) versus 22% (N = 37) in non-serous EC subjects Filing

3 more on record.

For subscribers

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