Biopharma Transcript

Aprea Therapeutics, Inc. APRE

Nasdaq · Phase 1 · oncology · small molecule · EDGAR · Updated Nov 5, 2026

Aprea Therapeutics, Inc. (Nasdaq: APRE) is an oncology drug developer. Its lead program, APR-1051, is in Phase 1 for PPP2R1A-mutated endometrial cancer (uterine serous carcinoma) and cyclin E-overexpressing platinum-resistant ovarian cancer. Its next catalyst on record is APR-1051: Clinical data update at 38th EORTC-NCI-AACR Symposium (November 2026).

Upcoming catalysts

  1. November 2026
    APR-1051 — Clinical data update at 38th EORTC-NCI-AACR SymposiumWe expect to report the next clinical data update from ACESOT-1051 at the 38th EORTC-NCI-AACR Symposium in November 2026.

Next further out: APR-1051 — Enrollment acceleration to 6-10 patients per month (Q4 2026). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
APR-246 (eprenetapopt)Undisclosed (discontinued program)small moleculePhase 3
ATRN-119Undisclosed (ATR inhibitor for oncology)small moleculePhase 2
APR-1051PPP2R1A-mutated endometrial cancer and cyclin E-overexpressing platinum-resistant ovarian cancersmall moleculePhase 1

Recent results and decisions

  1. May 6, 2026
    positive APR-1051 achieved a confirmed partial response in a patient with uterine carcinosarcoma harboring PPP2R1A mutation, with treatment ongoing at 140 days.Best Response: Confirmed Partial Response (PR) • PR (-50%) at first assessment Feb 10, 2026 • Confirmed PR with additional -9.5% reduction from C3D1 Mar 10, 2026 Filing

For subscribers

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