Aethlon Medical Publishes Long COVID Study Findings

Written by Emily J. Thompson, Senior Investment Analyst

Source: PRnewswire

Updated: Dec 02 2025

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Should l Buy AEMD?

Source: PRnewswire

Research Advancement: Aethlon Medical's preclinical study published on November 20, 2025, indicates that elevated extracellular vesicles in Long COVID plasma may provide a therapeutic target for Galanthus nivalis agglutinin (GNA) affinity resin, suggesting potential breakthroughs in Long COVID treatment.
Clinical Collaboration: The study, conducted in partnership with the UCSF Long COVID clinic, analyzed plasma samples from Long COVID patients and recovered controls, revealing significantly higher levels of extracellular vesicles in Long COVID patients, highlighting the device's potential application in treating post-COVID symptoms.
Technological Innovation: The Hemopurifier® device effectively removes harmful extracellular vesicles through plasma separation and GNA affinity resin, previously demonstrated in severe acute COVID-19 patients, indicating its potential efficacy in Long COVID patients and expanding its clinical application scope.
Market Potential: With Long COVID affecting 44 to 48 million people in the U.S. and an estimated economic burden of $2 billion, Aethlon's research findings could introduce new treatment options in this area, enhancing the company's competitiveness in the medical device market.

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About AEMD

Aethlon Medical, Inc. is a clinical-stage medical device company. The Company is focused on advancing the Hemopurifier (HP), a clinical-stage immunotherapeutic device intended for applications in cancer, life-threatening viral infections, and organ transplantation and other areas of significant unmet needs. In pre-clinical studies, the Hemopurifier has exhibited the capacity to remove harmful extracellular vesicles (EVs) and enveloped viruses from biological fluids, utilizing its proprietary lectin-based mechanism. These extracellular vesicles have been implicated in disease processes such as immune suppression and metastasis in cancer as well as in the progression of severe life-threatening infectious diseases. The United States Food and Drug Administration (FDA) has designated the Hemopurifier as a Breakthrough Device for the treatment of individuals with advanced or metastatic cancer who are unresponsive to or intolerant of standard of care therapy.

About the author

Emily J. Thompson

Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.

Aethlon Medical Schedules Q3 Financial Results Conference Call

4 days agoPRnewswire

Financial Results Announcement: Aethlon Medical will release its fiscal third-quarter financial results for the period ending December 31, 2025, on February 12, 2026, at 4:15 p.m. ET, highlighting advancements in cancer and life-threatening infectious disease treatments.
Conference Call Details: Management will host a conference call on the same day at 4:30 p.m. ET to review financial results and recent corporate developments, followed by a Q&A session to enhance interaction between investors and management.
Registration Process: Interested parties can register via a provided link to receive dial-in numbers, while those unable to pre-register can call the toll-free number 1-844-836-8741 or the international number 1-412-317-5442 to ensure participation in the call.
Hemopurifier Device Overview: Aethlon's Hemopurifier is a clinical-stage immunotherapeutic device designed to combat cancer and life-threatening viral infections, having received FDA Breakthrough Device designation, demonstrating potential in treating patients with refractory cancer.

Aethlon Medical Secures $3.3 Million Financing to Accelerate Cancer Treatment

Dec 05 2025PRnewswire

Financing Agreement: Aethlon Medical has entered into a securities purchase agreement with a single institutional investor to sell 595,897 shares and warrants for 1,042,820 shares, raising approximately $3.3 million, expected to close on December 8, 2025, enhancing liquidity for R&D support.
Warrant Inducement: The company has negotiated a warrant inducement agreement to lower the exercise price of March and September 2025 warrants to $4.03, which is expected to encourage the investor to exercise these warrants, providing additional funding for the company.
Market Compliance: This financing adheres to Nasdaq rules under Section 4(a)(2) of the Securities Act, ensuring the company's compliance in capital markets, which enhances investor confidence and improves the company's reputation.
Future Growth Potential: Aethlon is focused on developing the Hemopurifier to address unmet needs in oncology and infectious diseases, and this financing will accelerate clinical trial processes, boosting the company's competitiveness in the medical device sector.

American Eagle Shares Rise 15%; Check Out 20 Stocks Making Moves in Premarket Trading

Dec 03 2025Benzinga

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