Welcome to our dedicated page for AETHLON MEDICAL SEC filings (Ticker: AEMD), 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.
Aethlon Medical, Inc. filings document the regulatory record of a Nevada clinical-stage medical device company developing the investigational Aethlon Hemopurifier. Form 8-K reports cover quarterly financial results furnished under Regulation FD, material agreements tied to securities purchase arrangements, warrant-related capital-structure updates, and approved changes to the company's equity incentive plan.
Proxy materials cover annual-meeting and stockholder voting matters, including governance and compensation-plan proposals. Registration statements describe securities offered for sale, share-capital terms and related offering mechanics for the company's common stock and other securities.
Aethlon Medical, Inc. (AEMD) filed a Form 8-K reporting a material event dated September 4, 2025 that primarily attaches transaction documents and a press release. The filing includes forms of a Common Warrant, Pre-Funded Warrant, and a Placement Agent Warrant, a Warrant Agency Agreement with Computershare, a Securities Purchase Agreement with investors, a Placement Agency Agreement with Maxim Group, LLC, and a Press Release dated the same day.
The exhibits indicate the company executed a financing-related transaction structure involving warrants and a placement agent; the warrant agency relationship was documented with Computershare. The filing text is an exhibits list and does not disclose pricing, proceeds, or specific investor identities within the provided content.
Aethlon Medical, Inc. (AEMD) is offering common stock and pre-funded warrants in a best-efforts offering with no minimum, which could produce proceeds of approximately $4,218,750 before expenses based on the figures shown. The company agreed to pay a placement agent a 6.25% cash fee and issue placement agent warrants equal to 4.0% of the shares sold in the offering. If all inducement and company warrants are exercised, common shares outstanding would be 14,348,711.
The prospectus discloses significant risk factors: Aethlon has no current revenue streams, a history of operating losses, and substantial doubt about its ability to continue as a going concern for 12 months. Net tangible book value per share was $1.32 as of June 30, 2025. The company lists an extensive patent portfolio and global filings for devices and methods related to exosome removal and viral treatment. Shares trade on the Nasdaq Capital Market under AEMD; officers and directors are subject to a 60-day lock-up following this prospectus.
Aethlon Medical, Inc. (AEMD) filed an amended S-1 registration statement describing a best-efforts offering of up to 4,566,210 shares of common stock and related pre-funded warrants and placement-agent warrants. The company discloses it has no material revenue, a history of significant operating losses, and substantial doubt about its ability to continue as a going concern for 12 months without additional financing. Placement agent compensation includes a cash fee equal to 6.25% of gross proceeds and warrants equal to 4.0% of shares issued. Net tangible book value was $1.32 per share as of June 30, 2025. The filing highlights material dilution risks from outstanding warrants and reserved shares, regulatory and FDA compliance risks for its Hemopurifier and related technologies, numerous owned and pending patents across jurisdictions, and a 60-day lock-up by officers and directors.
Aethlon Medical, Inc. furnished an updated corporate investor presentation that may be used in conferences and investor meetings. The presentation, dated August 20, 2025, is available on the company’s website and is attached as Exhibit 99.1. The company emphasizes that this material is being provided under Regulation FD as “furnished, not filed,” meaning it is not subject to certain liability provisions of the securities laws and is not automatically incorporated into other SEC filings unless specifically referenced. This update is primarily an informational disclosure for investors and other stakeholders, rather than a report of new financial results or a major transaction.
Aethlon Medical, Inc. (AEMD) is filing an S-1 registration statement that covers a Company Offering and a resale by Selling Securityholders of up to 1,550,000 shares issuable upon exercise of inducement warrants. The prospectus discloses a history of significant operating losses, no current revenue streams, and expresses substantial doubt about the company’s ability to continue as a going concern for 12 months following its most recent financial statements. The offering is on a best-efforts basis with no minimum, so proceeds are presently undeterminable. Placement-agent compensation includes a 6.5% cash fee on gross proceeds and warrants equal to 4.0% of shares issued in the offering. Pre-funded warrants include a 4.99% beneficial ownership exercise blocker (expandable to 9.99% after notice). The company lists a broad patent portfolio across the U.S., Europe, Asia, Canada and other jurisdictions and states proceeds, if received, would be used for general corporate purposes, R&D, clinical trials and working capital.
Armistice Capital, LLC and Steven Boyd report beneficial ownership of 185,000 shares of Aethlon Medical Inc. Together they hold 7.16% of the outstanding common stock, based on 2,585,316 shares outstanding as of June 24, 2025. Armistice Capital is the investment manager of the Armistice Capital Master Fund Ltd., the direct holder of the shares, and exercises shared voting and dispositive power over the securities. Mr. Boyd, as managing member, is reported to share those voting and disposition rights. The Master Fund disclaims direct beneficial ownership due to its investment management agreement.
Aethlon Medical, Inc. (AEMD) reported a quarterly net loss of $1.76 million for the three months ended June 30, 2025, an improvement from $2.57 million a year earlier driven by lower payroll and professional fees. Revenue remained $0; operating expenses declined to $1.79 million from $2.62 million as headcount-related costs, severance and certain consulting fees decreased. Basic and diluted loss per share was ($0.85) versus ($2.76) in the prior year on a larger weighted-average share base of 2,076,416 shares.
Balance sheet highlights: cash and cash equivalents were $3.77 million, total assets $5.31 million, total liabilities $1.88 million, and stockholders' equity $3.42 million. Working capital fell to $2.42 million from $4.05 million at March 31, 2025. Management discloses substantial doubt about the company's ability to continue as a going concern and expects existing cash to be insufficient to fund operations for at least twelve months without additional financing.
Clinical and operational updates stated explicitly: the Hemopurifier phase 1 oncology trial is active at three Australian sites, three participants were treated in cohort 1 with no DSMB safety concerns, cohort 2 enrollment is open, the planned India trial (CDSCO-approved July 7, 2025) was cancelled to conserve resources, and a preprint reported >98% removal of platelet-derived EVs in an ex-vivo study. The company effected a 1-for-8 reverse stock split effective June 9, 2025 and maintains an open IDE for viral indications.