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Abeona Therapeut SEC Filings

ABEO NASDAQ

Welcome to our dedicated page for Abeona Therapeut SEC filings (Ticker: ABEO), 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.

Parsing a biotech filing is tough enough; add gene-therapy jargon and Abeona Therapeutics’ disclosures can feel impenetrable. Whether you are tracking cash runway for pivotal trials or gauging FDA feedback on its pz-cel program, each 8-K and 10-K is packed with scientific nuance investors can’t afford to miss.

Stock Titan turns that complexity into clarity. Our AI-powered summaries cut through the 200-page annual report so you immediately see clinical milestones, manufacturing expenditures, and risk factors—Abeona Therapeutics annual report 10-K simplified. Need fresh numbers? The Abeona Therapeutics quarterly earnings report 10-Q filing posts here seconds after EDGAR releases, complete with trend charts and a plain-English breakdown. Material news arrives first via Abeona Therapeutics 8-K material events explained, while understanding Abeona Therapeutics SEC documents with AI means no more deciphering footnotes alone.

Curious about management’s own trades before key read-outs? Our real-time alerts surface every Abeona Therapeutics insider trading Form 4 transactions, plus historical context for Abeona Therapeutics executive stock transactions Form 4. You’ll also find the Abeona Therapeutics proxy statement executive compensation with easy-to-scan pay tables and governance scores. Below is everything available in one place:

  • 10-K and 10-Q filings with AI commentary—Abeona Therapeutics earnings report filing analysis
  • 8-K event notices covering trial data, financings and CMC updates
  • Abeona Therapeutics Form 4 insider transactions real-time feed
  • DEF 14A proxy statements for compensation and voting matters

All documents refresh automatically, so the moment Abeona files, you’re already informed.

Filing
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Abeona Therapeutics Inc. (ABEO) filed a Form 144 indicating that insider Joseph Vazzano intends to sell up to 25,335 common shares through broker Stifel Nicolaus on or about 07 July 2025 (approximate sale date 07/09/2025). The proposed transaction carries an aggregate market value of $148,354, equal to roughly 0.05 % of the company’s 51.16 million shares outstanding, and follows a prior sale of 17,795 shares for $120,314 on 06 June 2025. The stock to be sold originates from 51,733 restricted-stock units acquired on 07 July 2025 and qualifies for resale under Rule 144.

The filing contains no operational or financial updates and merely provides advance notice of a relatively small insider sale. Given the modest size of the transaction versus Abeona’s float, the market impact is expected to be minimal, although investors may monitor cumulative insider activity for sentiment cues.

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Filing
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ENDRA Life Sciences Inc. (Nasdaq: NDRA) filed a Form 8-K on 9 July 2025 to report that it has submitted a Form S-1 registration statement with the SEC. The S-1 covers a proposed public offering of the company’s common stock and accompanying warrants. The filing also notes that the Prospectus attached to the S-1 (incorporated in the 8-K as Exhibit 99.1) contains preliminary, unaudited financial results for the fiscal quarter ended 30 June 2025. No quantitative financial figures or offering terms (such as number of shares, warrant ratio, pricing range, or expected gross proceeds) are included in the 8-K itself. The company specifies that the information furnished under Item 2.02 and Exhibit 99.1 is not deemed “filed” for purposes of Section 18 of the Exchange Act and may only be incorporated by reference if expressly stated in future filings. Other than identifying the CFO as the signing officer, the report provides no additional operational or financial details.

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Filing
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Methode Electronics, Inc. (NYSE: MEI) filed its Form 10-K for the 53-week fiscal year ended 3 May 2025. The report confirms MEI’s status as an accelerated filer and outlines a global organisation of roughly 6,500 employees and 800 contractors across North America, EMEA and Asia.

Business model and segments. Methode operates three continuing segments—Automotive, Industrial and Interface—after discontinuing and largely divesting its Medical unit (Dabir Surfaces) in FY24. Segment mix shifted materially year-over-year:

  • Automotive: 48.6 % of FY25 net sales (down from 53.7 % in FY24 and 62.4 % in FY23) as certain centre-console and EV programmes rolled off.
  • Industrial: 46.5 % (up from 41.3 % in FY24 and 32.6 % in FY23) driven by lighting, busbar and power-distribution products.
  • Interface: 4.9 % (little changed versus prior years).
The five largest customers accounted for ~36 % of consolidated revenue in FY25, but no single customer exceeded 10 %.

Strategic highlights. • Accelerated diversification away from automotive as Industrial gains share.
• R&D spending remained robust at $41.8 million (FY25) versus $49.1 million (FY24) and $35.0 million (FY23).
• A new CEO, Jonathan DeGaynor, was appointed, emphasising talent alignment and inclusivity.

Capital structure. The company’s $400 million revolving credit facility had $319.4 million outstanding at year-end. Methode was out of compliance with its leverage and interest-coverage covenants as of 3 May 2025 but secured a waiver and amendment on 7 Jul 2025. The facility includes an “anti-cash-hoarding” clause requiring prepayment of excess U.S. cash above $65 million.

Risk landscape. Management lists extensive risk factors, notably: dependence on cyclical automotive, commercial-vehicle and construction markets; lower-than-expected EV adoption prompting OEM programme cancellations; inflationary cost pressure; global supply-chain constraints; concentration of large customers; unionised labour abroad; variable-rate debt exposure; and the need to comply with tightened credit covenants. Additional operational risks include pricing pressure, rapid technology shifts, and geopolitical uncertainty.

Human capital & ESG. 95 % of employees are outside the U.S.; the company highlights diversity, safety and compliance training. No environmental capital-spending needs deemed material to date.

Key takeaways for investors: Methode is navigating a pivot toward industrial applications while wrestling with automotive programme roll-offs and covenant pressure. Revenue diversification, solid R&D investment and no single-customer dominance are favourable, but leverage, EV-demand volatility and price-down pressures temper the outlook.

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Filing
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Schedule 13D/A highlights Tang Capital Management, Kevin Tang and affiliated investment vehicles disclosed updated ownership and transaction details regarding Cargo Therapeutics, Inc. ("CRGX").

  • Beneficial ownership: The reporting group controls 3,059,630 common shares, representing 6.6 % of the 46,113,353 shares outstanding. Voting and dispositive power over the shares is shared among Tang Capital Management, Tang Capital Partners (TCP), Tang Capital Partners International (TCPI) and Kevin Tang.
  • Source of funds: Approximately $22 million of working capital from TCP and TCPI, held in margin accounts, was used to acquire the stake.
  • New strategic development – signed Merger Agreement (7 July 2025):
    • Buyer: Concentra Biosciences, LLC; vehicle: Concentra Merger Sub VII, Inc.
    • Tender-offer price: $4.379 in cash per CRGX share plus one contingent value right (CVR).
    • Subsequent merger: Merger Sub will merge into Cargo Therapeutics, with Cargo surviving as a Concentra subsidiary.
    • Key closing conditions: (i) >50 % of outstanding shares tendered; (ii) Closing Net Cash ≥ $217.5 million; (iii) customary regulatory and procedural conditions.
    • Limited guaranty: TCP provided a guarantee capped at $213.1 million for certain obligations under the Merger Agreement.
    • CVR structure: Holders will be entitled to (i) 100 % of Closing Net Cash above $217.5 million, and (ii) 80 % of net proceeds from any sale, transfer or license of CRG-022, CRG-023 or the company’s allogeneic platform occurring within two years post-merger, subject to a $250 k expense cap.
  • No recent trading activity: The reporting persons executed no CRGX share transactions during the past 60 days.

The amendment primarily informs investors of the cash-and-CVR takeover proposal, outlines financial protections (guaranty, cash threshold) and updates the group’s unchanged 6.6 % ownership position.

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Filing
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Jupiter Neurosciences, Inc. (Nasdaq: JUNS) filed an 8-K on 2 July 2025 disclosing Compensation Committee approval of a one-time bonus package for key executives.

Equity component: The committee granted an aggregate 357,448 stock options under the 2023 Equity Incentive Plan: 255,320 to Chief Business Officer Alison Silva and 102,128 to CFO Saleem Elmassri. All options carry a $1.19 exercise price (the 2 July 2025 closing price), a 10-year term, and three-year ratable vesting starting on the grant date, contingent on continued employment. Any shares issued upon exercise will be fully paid and non-assessable.

Cash component: Cash bonuses are conditioned on the company achieving >$3.5 million cash on hand. When this liquidity trigger is met, the following payments will be made: CEO Christer Rosén $210,000; CBO Alison Silva $45,000; CSO Marshall Hayward $50,000; CAO Alexander Rosén $72,000; Titan Advisory Services $72,000. No timetable is provided for meeting the cash threshold.

The committee cited management’s role in the December 2024 IPO, willingness to defer 2024 compensation, and forgiveness of company debts as justification. No other operational or financial metrics were disclosed in this filing.

Investor considerations: The option grants represent potential dilution at a strike near current market price, aligning management incentives with shareholder value over a three-year horizon. However, the contingent cash bonuses suggest liquidity remains constrained, and future payouts will draw on available cash once the threshold is met.

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Filing
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GS Finance Corp., a subsidiary of The Goldman Sachs Group, Inc., is issuing $592,000 of Autocallable Equity-Linked Notes due July 15, 2030 under its Series F medium-term note program. The notes are fully and unconditionally guaranteed by The Goldman Sachs Group, Inc. and will be sold at 100% of face value on the original issue date of July 10 2025.

Structure: the zero-coupon notes provide two potential payment scenarios:

  • Automatic call – If, on the single call observation date (July 7 2027), the closing price of each reference stock (UNH, CRWD, AMZN, PLTR, NVDA) is ≥ 80% of its initial price, the notes are redeemed early for $1,450 per $1,000 face amount (45.0% gross return, ≈18% IRR).
  • Maturity payment – If not called, holders receive on July 15 2030:
    • Face amount × [1 + 100% × lesser-performing stock return] if each final price > initial price.
    • Face amount ($1,000) if any final price ≤ initial price.

Reference stock initial prices: UNH $303.71; CRWD $505.46; AMZN $223.47; PLTR $139.12; NVDA $158.24 (all recorded on trade date 07-07-25).

Economics & fees: underwriting discount 1.125%; net proceeds 98.875%. The estimated value at pricing is $938 per $1,000, reflecting model value minus fees and hedging spread. GS &Co.’s bid/ask adjustment ($62) amortises to zero by 10-07-25, after which secondary quotes align with the model value.

Risk / return profile:

  • Principal preservation – No loss of principal provided GS and guarantor remain solvent.
  • Upside capped – 45% maximum via automatic call; otherwise uncapped but only if all five stocks rise.
  • Worst-of basket – Maturity upside linked to single worst performer; any lagging stock nullifies growth.
  • Credit risk – Payments depend on GS Finance Corp. and The Goldman Sachs Group, Inc.
  • Liquidity – No listing; market-making discretionary; investors may face wide spreads.
  • Valuation discount – Issue price exceeds model value by 6.2%, creating negative carry if sold early.

Key dates: Trade 07-07-25 | Issue 07-10-25 | Call observation 07-07-27 | Call payment 07-14-27 | Determination 07-08-30 | Maturity 07-15-30.

Investors seeking equity exposure with principal protection and potential for a 45% pre-maturity return may find the notes attractive, but must weigh valuation discount, concentration in five high-beta technology / healthcare names, call risk, and Goldman Sachs credit exposure.

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Filing
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GCL Global Holdings Ltd ("GCL") has filed Prospectus Supplement No. 8 and a Form 6-K to disclose a new warrant issuance linked to an existing SG$5 million credit facility extended to its wholly-owned subsidiary, Epicsoft Asia Pte. Ltd.

  • Financing context: The facility, arranged with Oversea-Chinese Banking Corporation (OCBC) on 1 Oct 2024 and amended 12 Mar 2025, provides up to SG$5 million (≈ US$3.75 million). One condition precedent for draw-down is issuance of a warrant to OCBC.
  • Warrant terms: • Shares underlying warrant: 899,281 ordinary shares • Exercise price: US$4.17 per share • Aggregate exercise proceeds: US$3.75 million • Term: 5 years from 7 Jul 2025 • Automatic exercise triggers if (i) VWAP > US$12 for 20 consecutive trading days, (ii) ≥ 1 million average daily volume, (iii) market cap ≥ US$1 billion, and (iv) an effective resale registration statement is available.
  • Use of proceeds: All exercise proceeds will first repay outstanding amounts under the OCBC facility; any excess is earmarked for the subsidiary’s working capital.
  • Dilution & registration: The warrant represents potential dilution of ~899k shares (≈ 1.1% of the 83.5 million shares covered by the broader resale prospectus). GCL must file a resale registration statement for these warrant shares within six months (by 7 Jan 2026).
  • Listing & compliance: Shares are listed on Nasdaq Global Select Market; GCL commits to maintain listing, register shares, and provide customary registration rights, indemnities and adjustment mechanisms.

The filing primarily informs investors of incremental potential dilution, outlines the company’s obligations to register the warrant shares, and clarifies that any cash from warrant exercise will reduce debt associated with the SG$5 million facility. No new earnings or operational metrics are provided.

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On June 27, 2025 Abeona Therapeutics Inc. (“Abeona”) closed the previously announced sale of its Rare Pediatric Disease Priority Review Voucher (PRV) to an undisclosed buyer for $155 million in gross cash proceeds under the asset purchase agreement dated May 9, 2025. The voucher had been granted by the FDA on April 28, 2025 following approval of Abeona’s BLA for ZEVASKYN™ (prademagene zamikeracel). The transaction is reported in this Form 8-K under Item 2.01.

In a press release furnished with the filing (Exhibit 99.1) the company disclosed that, including the net PRV proceeds, unaudited cash, cash equivalents, restricted cash and short-term investments stood at approximately $225 million as of June 30, 2025. Management notes the figure is preliminary, unaudited and subject to quarter-end closing procedures; the independent auditor has not reviewed the estimate.

The agreement itself will be filed with Abeona’s forthcoming Form 10-Q. No other material liabilities, guidance changes or pro-forma financials were provided.

The sale injects substantial non-dilutive capital and materially strengthens the company’s liquidity profile while removing the PRV from Abeona’s asset base.

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FAQ

What is the current stock price of Abeona Therapeut (ABEO)?

The current stock price of Abeona Therapeut (ABEO) is $5.83 as of July 9, 2025.

What is the market cap of Abeona Therapeut (ABEO)?

The market cap of Abeona Therapeut (ABEO) is approximately 284.9M.

What is the primary focus of Abeona Therapeutics Inc?

Abeona Therapeutics Inc is focused on developing innovative gene and cell therapies for life‐threatening rare genetic diseases, leveraging advanced biotechnologies.

What type of technologies does Abeona utilize in its research?

The company employs advanced technologies including adeno-associated virus (AAV)-based vectors and CRISPR/Cas9 gene editing to address genetic abnormalities in rare diseases.

How does Abeona develop its therapies?

Abeona develops its therapies through a robust clinical-stage pipeline, combining innovative genetic therapeutic approaches with strategic collaborations and rigorous regulatory oversight.

What is the role of regulatory compliance in Abeona's operations?

Regulatory compliance is integral to Abeona’s operations; the company adheres to stringent FDA standards, ensuring quality in manufacturing and clinical trial processes to maintain safety and efficacy.

How does Abeona’s pipeline reflect its commitment to innovation?

The pipeline includes diverse approaches such as AAV-based gene therapies and autologous cell therapy platforms, underscoring the company’s commitment to versatility and precision in treating rare genetic diseases.

What significance do FDA inspections and regulatory milestones have for Abeona?

Successful FDA inspections and favorable regulatory assignments demonstrate Abeona’s commitment to high manufacturing and operational standards, crucial for the safe development of advanced therapeutic products.

How does Abeona differentiate itself from competitors?

Abeona sets itself apart through its focus on precision medicine for rare diseases, its use of cutting-edge gene therapy technologies, and its dedication to strict regulatory compliance and quality manufacturing.

What are the key challenges faced by clinical-stage biotech companies like Abeona?

Key challenges include navigating complex regulatory environments, ensuring high standards in clinical trial execution, and managing the risks associated with advanced biotechnological research and development.
Abeona Therapeut

NASDAQ:ABEO

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ABEO Stock Data

284.94M
48.02M
5.45%
76.5%
5.8%
Biotechnology
Pharmaceutical Preparations
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United States
CLEVELAND