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Aprea Therapeutics APRE · USD

Health Care · US listing · 🇺🇸 United States

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0.50

-3.21%

Close of 9 Nov 2026, in USD

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About Aprea Therapeutics

From its filings with the US Securities and Exchange Commission

SEC filings

Aprea Therapeutics is based in Doylestown, Pennsylvania and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker APRE. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported a net loss of $12.6m. At that date it held total assets of $15.9m and shareholders' equity of $12.4m.

In its own words

We are a clinical-stage precision medicine oncology company focused on the discovery and development of targeted therapies for patients with biomarker-defined cancers. Our approach focuses on matching treatments to specific cancer-related genetic mutations to potentially maximize effectiveness and minimize side effects. Specifically, we develop small molecule inhibitors designed to exploit genetic mutations in cancer to widen the therapeutic window and intended to make treatments more effective at destroying cancer cells while sparing healthy tissue. We have assembled a team with extensive experience in the discovery, development, and commercialization of oncology drugs to support our mission of developing novel synthetic lethality-based cancer therapeutics.

Aprea Therapeutics AB was originally incorporated in 2002 and commenced principal operations in 2006. On September 20, 2019, we consummated a reorganization, pursuant to which all of the issued and outstanding stock and options of Aprea Therapeutics AB were exchanged for common stock, preferred stock or options, as applicable, of Aprea Therapeutics, Inc. As a result, Aprea Therapeutics AB became a wholly-owned subsidiary of Aprea Therapeutics, Inc.

Quoted from its 10-K, filed 16 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
3 Oct 2019
Employees
8
Website
aprea.com ↗
Head office
3805 OLD EASTON ROAD, DOYLESTOWN, PA, 18902
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Dr. Richard PetersIndependent Chairman of the Board$97,431
  • Dr. Oren GiladPresident, Chief Executive Officer, Director, since 2022$760,091
  • Mr. John HamillChief Financial Officer, Senior Vice President, Secretary$536,649
  • Dr. Nadeem MirzaChief Medical Officer$447,738
  • Mr. John HennemanLead Independent Director$75,431
  • Dr. Jean-Pierre BizzariIndependent$44,000
  • Mr. Marc DueyIndependent Director$62,431
  • Mr. Michael GrissingerIndependent Director$71,931
  • Dr. Gabriela GruiaIndependent Director$44,000
  • Dr. Rifat PamukcuIndependent Director$70,431
  • Dr. Bernd SeizingerIndependent Director$75,931

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
39
Environment
18
Social
74
Governance
23
Women in the workforce
50%
Carbon reduction policy
No
Human rights policy
No

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Headquartered in Boston, Massachusetts, a major biotech hub.
  • Focuses on developing cancer therapeutics targeting mutant p53 tumor suppressor protein.
  • Lead product candidate APR-246 is in clinical development for hematologic malignancies.

Weaknesses

  • Operates with only 8 employees, indicating limited workforce capacity.
  • IPO occurred in 2019, suggesting a relatively young company with limited market history.
  • Relies on a single lead product candidate, APR-246, for development focus.

Opportunities

  • Potential for APR-246 to address unmet needs in MDS and AML treatments.
  • Development of APR-548 as an oral p53 reactivator could expand therapeutic options.
  • Clinical-stage focus may attract partnerships or investment for further development.

Threats

  • Dependence on a single product candidate could pose significant risk if development fails.
  • Biotechnology sector is highly competitive with numerous players targeting similar therapies.
  • Regulatory approval processes for cancer therapeutics are lengthy and uncertain.

Sources and methodology

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