1.58
-1.86%
Close of 9 Nov 2026, in USD
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About Acrivon Therapeutics
From its filings with the US Securities and Exchange Commission
Acrivon Therapeutics is based in Watertown, Massachusetts. Its shares trade on Nasdaq under the ticker ACRV. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported a net loss of $77.9m. At that date it held total assets of $129.7m and shareholders' equity of $112.5m.
We are a clinical-stage biopharmaceutical company discovering and developing precision medicines utilizing our proprietary Generative Phosphoproteomics Acrivon Predictive Precision Proteomics, or AP3, platform designed to quantify compound-specific, drug-regulated pathway activity levels inside the intact cell in an unbiased manner, yielding terabytes of proprietary data and delivering rapid, actionable insights. Our company name, Acrivon, is derived from Greek for “accurate” or “precise”. We chose it to embody how our AP3 platform can, among other highly actionable discovery and development applications, accurately match our therapies with patients who will benefit. Recently approved precision oncology treatments, such as kinase inhibitors, have transformed the cancer treatment landscape, and while the therapeutic benefit of these agents has provided significant benefit to patients, these precision oncology treatments unfortunately only address the less than 10% of patients with cancers that harbor certain easily-identifiable genetic mutations. Our approach is designed to overcome the limitations of genetics-based precision medicine. We do this by using our precision medicine platform, AP3, to discover and develop our pipeline of innovative oncology drug candidates. AP3 is engineered to measure compound-specific effects on the entire tumor cell protein, signaling network and drug-induced resistance mechanisms in an unbiased manner and is modality and disease agnostic.
Quoted from its 10-K, filed 19 Mar 2026. Read the filing on SEC.gov ↗
Company facts
- Sector
- Health Care
- Industry
- Biotechnology
- Listed since
- 15 Nov 2022
- Employees
- 56
- Website
- acrivon.com ↗
- Head office
- 480 ARSENAL WAY, SUITE 100, WATERTOWN, MA, 02472
- Classification
- Pharmaceutical Preparations
- Filer status
- <br>Emerging growth company
Leadership
Pay as last reported
- Dr. Peter Blume-JensenChairman of the Board, President, Chief Executive Officer, since 2018$2.0m
- Dr. Adam LevyChief Financial Officer, Principal Financial Officer
- Dr. Eric DevroeChief Operating Officer$1.1m
- Dr. Kristina MassonExecutive Vice President - Business Operations, Director, since 2018$1.2m
- Dr. Erick GamelinChief Development Officer$538,078
- Mrs. Mary-Alice MillerChief Legal Officer$697,003
- Dr. Raza MirzaChief Medical Officer
- Dr. Charles BaumIndependent Director$152,286
- Dr. Derek DiroccoIndependent Director$151,036
- Dr. Ivana Magovcevic-LiebischIndependent Director$122,476
- Mr. Santhosh PalaniIndependent Director$188,330
- Dr. Sharon ShachamIndependent Director$142,286
Environmental, social and governance
Scores out of 100, from our data supplier
- Overall
- 28
- Environment
- 31
- Social
- 29
- Governance
- 26
- Carbon reduction policy
- No
- Human rights policy
- Yes
SWOT analysis
AI-generated by our data supplier. Not written or checked by our editors.
Strengths
- Acrivon Therapeutics' AP3 platform enables precise oncology drug development with ACR-368 in Phase II trials.
- ACR-368 OncoSignature test improves clinical response rates for platinum-resistant ovarian cancer patients.
- The company's pipeline includes two preclinical programs targeting WEE1 and PKMYT1 inhibitors.
Weaknesses
- Acrivon Therapeutics has only 56 employees, limiting operational capacity.
- The company's IPO occurred in November 2022, indicating limited market history.
- Acrivon's focus on oncology drugs may restrict diversification opportunities.
Opportunities
- ACR-368's Phase II trials across multiple solid tumor types could expand market reach.
- The AP3 platform's predictive capabilities may attract partnerships in oncology research.
- The firm's preclinical programs could lead to new drug approvals in the oncology sector.
Threats
- Competition in the oncology drug market may impact ACR-368's commercial success.
- Regulatory challenges could delay the approval of ACR-368 and other pipeline candidates.
- The biotechnology sector faces high R&D costs that may strain financial resources.
Sources and methodology
- Data on this tab
- Our data supplier
- Chart on the Overview
- TradingView
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