| Symbol | APRE |
|---|---|
| Name | APREA THERAPEUTICS, INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Pharmaceutical Preparations |
| Address | 535 BOYLSTON STREET, BOSTON, Massachusetts, 02116, United States |
| Telephone | +1 617 463-9385 |
| Fax | — |
| — | |
| Website | https://www.aprea.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | — |
| Description | Aprea Therapeutics Inc is a clinical-stage biopharmaceutical company focused on developing and commercializing cancer therapeutics that reactivate mutant p53 tumor suppressor protein. Its product candidate, APR-246, is a small molecule p53 reactivator that is in late-stage clinical development for hematologic malignancies, including myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). Additional info from NASDAQ: |
New Form S-3 - Aprea Therapeutics, Inc. <b>Filed:</b> 2026-04-22 <b>AccNo:</b> 0001104659-26-046900 <b>Size:</b> 524 KB
Read moreAprea Therapeutics to Provide Clinical Update on ACESOT-1051 Phase 1 Trial Evaluating WEE1 Inhibitor, APR-1051, at ASCO 2026 Annual Meeting
Read moreNew Form PRE 14A - Aprea Therapeutics, Inc. <b>Filed:</b> 2026-04-20 <b>AccNo:</b> 0001104659-26-045158 <b>Size:</b> 2 MB
Read moreNew Form SCHEDULE 13G - Aprea Therapeutics, Inc. <b>Filed:</b> 2026-04-07 <b>AccNo:</b> 0002050709-26-000012 <b>Size:</b> 81 KB
Read moreHamill John P. 🟢 acquired 62.0K shares (2 derivative) of Aprea Therapeutics, Inc. (APRE) at $0.68 Transaction Date: Mar 31, 2026 | Filing ID: 038522
Read moreDirector Peters Richard 🟢 acquired 247.8K shares (2 derivative) of Aprea Therapeutics, Inc. (APRE) at $0.68 Transaction Date: Mar 31, 2026 | Filing ID: 038518
Read more(99% Neutral) APREA THERAPEUTICS, INC. (APRE) Announces Clinical Development Update
Read moreAprea Therapeutics Announces Oversubscribed $30 Million Private Placement
Read moreNew Form EFFECT - Aprea Therapeutics, Inc. <b>Filed:</b> 2026-03-19 <b>AccNo:</b> 9999999995-26-000871 <b>Size:</b> 1 KB
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT06260514 | Study of APR-1051 in Patients With Advanced Solid Tumors | Phase1 | Advanced Solid Tumor | Recruiting | 2024-06-13 | 2028-06-01 | ClinicalTrials.gov |
| NCT04905914 | Study Of ATRN-119 In Patients With Advanced Solid Tumors | Phase1 | Advanced Solid Tumor | Active_Not_Recruiting | 2023-01-09 | 2028-02-01 | ClinicalTrials.gov |
| NCT04638309 | APR-548 in Combination With Azacitidine for the Treatment of TP53 Myelodysplast… | Phase1 | MDS | Terminated | 2021-09-20 | 2022-04-25 | ClinicalTrials.gov |
| NCT04419389 | APR-246 in Combination With Acalabrutinib or Venetoclax Based Therapy in Subjec… | Phase1 | Non Hodgkin Lymphoma | Terminated | 2021-03-02 | 2021-08-24 | ClinicalTrials.gov |
| NCT03588078 | Study of the Safety and Efficacy of APR-246 in Combination With Azacitidine | Phase1 | Myelodysplastic Syndrome With Gene Mutation | Unknown | 2018-09-15 | 2021-05-15 | ClinicalTrials.gov |
| NCT03391050 | A Study of APR-246 in Combination With Dabrafenib in Resistant Patients With BR… | Phase1 | Melanoma | Terminated | 2018-01-18 | 2018-08-08 | ClinicalTrials.gov |
| NCT03072043 | Phase 1b/2 Safety and Efficacy of APR-246 w/Azacitidine for tx of TP53 Mutant M… | Phase1 | Myelodysplastic Syndrome | Completed | 2017-05-18 | 2021-12-08 | ClinicalTrials.gov |
| NCT00900614 | Safety Study of APR-246 in Patients With Refractory Hematologic Cancer or Prost… | Phase1 | Hematologic Neoplasms | Completed | 2009-05-01 | 2010-10-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | Other | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| APR-1051 | DRUG | Phase PHASE1 | Advanced Solid Tumor | RECRUITING | NCT06260514 |
| ATRN-119 | DRUG | Phase PHASE1 | Advanced Solid Tumor | ACTIVE_NOT_RECRUITING | NCT04905914 |
| APR-548 + Azacitidine | DRUG | Phase PHASE1 | MDS | TERMINATED | NCT04638309 |
| APR-246 (eprenetapopt) 4.5 g/d + Venetoclax + Rituximab in RT | DRUG | Phase PHASE1 | Non Hodgkin Lymphoma | TERMINATED | NCT04419389 |
| APR-246 (eprenetapopt) 4.5 g/d + (Acalabrutinib, OR, (Venetoclax +Rituximab)), in CLL and/or MCL and/or RT | DRUG | Phase PHASE1 | Non Hodgkin Lymphoma | TERMINATED | NCT04419389 |
| APR-246 (eprenetapopt) 4.5 g/d + Venetoclax + Rituximab in CLL | DRUG | Phase PHASE1 | Non Hodgkin Lymphoma | TERMINATED | NCT04419389 |
| APR-246 (eprenetapopt) + Acalabrutinib in CLL | DRUG | Phase PHASE1 | Non Hodgkin Lymphoma | TERMINATED | NCT04419389 |
| APR-246 (eprenetapopt) + Pembrolizumab | DRUG | Phase PHASE1 | Bladder Cancer | COMPLETED | NCT04383938 |
| Venetoclax | DRUG | Phase PHASE1 | Myeloid Malignancy | COMPLETED | NCT04214860 |
| APR-246 + azacitidine | DRUG | Phase PHASE3 | MDS | COMPLETED | NCT03745716 |
| Dabrafenib | DRUG | Phase PHASE1 | Melanoma | TERMINATED | NCT03391050 |
| Pegylated Liposomal Doxorubicin Hydrochloride (PLD) | DRUG | Phase PHASE2 | High-grade Serous Ovarian Cancer | COMPLETED | NCT03268382 |
| Azacitidine | DRUG | Phase PHASE1 | Myeloid Malignancy | COMPLETED | NCT04214860 |
| Carboplatin and Pegylated Liposomal Doxorubicin Hydrochloride (PLD) | DRUG | Phase PHASE1 | Platinum Sensitive Recurrent High-grade Serous Ovarian Cancer With Mutated p53 | COMPLETED | NCT02098343 |
| APR-246 | DRUG | Phase PHASE1 | Myeloid Malignancy | COMPLETED | NCT04214860 |