STOCK TITAN

Acrivon Therapeutics, Inc. SEC Filings

ACRV NASDAQ

Welcome to our dedicated page for Acrivon Therapeutics SEC filings (Ticker: ACRV), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.

Clinical-stage biotech filings can read like a graduate textbook—especially when Acrivon Therapeutics packs its 10-K with proteomics jargon, trial protocols, and liquidity tables. If you’re searching “Acrivon Therapeutics SEC filings explained simply” or wondering how platinum-resistant ovarian cancer data affects the balance sheet, you’re in the right place. Stock Titan’s AI dissects every page the moment it hits EDGAR, so you spend minutes—not hours—finding what matters.

Need to track “Acrivon Therapeutics insider trading Form 4 transactions” before the next readout? Our dashboard streams Form 4 insider transactions in real time, flags option exercises, and links them to upcoming milestones disclosed in 8-Ks. Curious about cash runway? The quarterly earnings report 10-Q filing is paired with plain-English summaries that spotlight R&D spend, burn rate, and AP3 platform progress. We also map risk-factor changes between annual report 10-K filings, highlight any shelf-registration clues in S-3s, and surface board votes from the latest proxy statement on executive compensation.

Whether you’re parsing an “Acrivon Therapeutics earnings report filing analysis,” monitoring “Acrivon Therapeutics executive stock transactions Form 4,” or decoding an “Acrivon Therapeutics 8-K material events explained,” Stock Titan delivers comprehensive coverage. Our AI-powered summaries translate dense pathway diagrams into actionable insights, while expert commentary points out dilution risk and regulatory catalysts. Set custom alerts to know the second a new study start appears, compare segment performance across periods, and keep a pulse on WEE1/PKMYT1 clinical updates. All ACRV filings, all in one place, always up to date.

Rhea-AI Summary

Nelnet, Inc. (NNI) – Form 4 filed 07/21/2025

Director and >10% owner Angela L. Muhleisen reported a Code G gift of 41,250 Class A shares on 07/17/2025 at $0.00 per share. Her direct holdings fall to 972,199 shares (down c. 4%).

She continues to report ~2.23 million additional shares held indirectly through her late spouse’s estate (1.23 m) and multiple dynasty trusts/GRATs, bringing total reported beneficial ownership to roughly 3.2 million shares. The filing states that 857,353 shares held by her adult son and 869,025 shares held by her adult daughter are no longer included in her reportable holdings.

No open-market sales, purchases, or derivative transactions were disclosed; the activity appears related to estate or family wealth planning and is unlikely to affect Nelnet’s capital structure or liquidity.

Rhea-AI Impact
Rhea-AI Sentiment
End-of-Day
-- %
Tags
insider

FAQ

What is the current stock price of Acrivon Therapeutics (ACRV)?

The current stock price of Acrivon Therapeutics (ACRV) is $1.39 as of July 22, 2025.

What is the market cap of Acrivon Therapeutics (ACRV)?

The market cap of Acrivon Therapeutics (ACRV) is approximately 41.7M.

What is the primary focus of Acrivon Therapeutics?

Acrivon Therapeutics specializes in precision oncology by developing targeted drugs using its proprietary proteomics-based AP3 platform to identify patients likely to benefit from specific treatments.

How does the AP3 platform work?

The AP3 platform integrates global proteomics and digital imaging to measure compound-specific effects on tumor cell protein signaling networks, which aids in designing drug-tailored biomarker signatures and companion diagnostics.

What are Acrivon’s key pipeline programs?

The company’s key programs include ACR-368, a selective inhibitor targeting CHK1 and CHK2, and ACR-2316, a dual inhibitor targeting WEE1/PKMYT1, both developed to address critical pathways in oncology.

How does Acrivon select patients for its clinical trials?

Acrivon uses its OncoSignature companion diagnostics, which are generated through the AP3 platform, to prospectively identify patients whose tumors exhibit the biomarker signatures indicating sensitivity to its drug candidates.

What differentiates ACR-368 from other oncology therapies?

ACR-368 is distinct because it is developed based on a mechanistic understanding of checkpoint kinases, leveraging a proteomics-driven approach to ensure that the therapy is matched with patients most likely to benefit.

How does Acrivon support its drug development process?

The company incorporates comprehensive proteomic analyses and digital imaging to gather high-resolution data on tumor biology, ensuring that its drug design is accurately aligned with patient-specific tumor mechanisms.

What role do companion diagnostics play in Acrivon’s strategy?

Companion diagnostics, such as the OncoSignature assay, are pivotal to Acrivon’s strategy as they enable the precise identification of patients most likely to respond to its targeted therapies, thereby enhancing treatment efficacy.

How is Acrivon positioned within the competitive precision oncology landscape?

Acrivon leverages its unique AP3 platform to deliver detailed proteomic insights and targeted drug design, setting a high standard for precision medicine in oncology and differentiating it from competitors who use traditional screening methods.
Acrivon Therapeutics, Inc.

NASDAQ:ACRV

ACRV Rankings

ACRV Stock Data

41.70M
24.82M
22.06%
74.97%
2.4%
Biotechnology
Pharmaceutical Preparations
Link
United States
WATERTOWN