Aethlon Medical

Aethlon Medical

AEMD
Is this your company? Claim your profile to update info and connect with investors.
Claim profile

Private Company

Total funding raised: $43M

Market Cap: $3.8MFounded: 1999Employees: 11-50HQ: San Diego, United States

Overview

Aethlon Medical is a clinical-stage biotech focused on developing its proprietary Hemopurifier® device, a lectin-affinity blood filter designed as an adjunctive therapy to remove immunosuppressive exosomes in cancer and enveloped viruses in infections. Its key achievements include securing dual FDA Breakthrough Device designations and advancing an ongoing safety and feasibility trial in oncology patients in Australia. The company's strategy leverages this regulatory pathway to accelerate development in two high-need areas, aiming to validate a platform that could enhance the efficacy of existing immunotherapies and provide a rapid-response tool for pandemic threats.

OncologyInfectious Disease

Technology Platform

The Hemopurifier® is a lectin-affinity based blood filtration device designed to selectively remove specific glycosylated targets from circulation, including immunosuppressive tumor-derived exosomes in cancer and enveloped viruses in infectious disease.

Funding History

7
Total raised:$43M
PIPE$5M
PIPE$8M
IPOUndisclosed
Series C$15M

Opportunities

The Hemopurifier addresses the massive unmet need of immunotherapy resistance in oncology by targeting tumor-derived exosomes, potentially expanding the population of responders.
Its broad-spectrum mechanism also presents a strategic opportunity in government-funded pandemic preparedness as a rapid-response countermeasure against novel viral threats.

Risk Factors

The company faces significant clinical risk that its technology may not demonstrate efficacy, severe financial risk due to its pre-revenue status and dependence on dilutive financings, and regulatory/commercialization risk in bringing a novel device to market.

Competitive Landscape

Aethlon faces limited direct competition, with its primary differentiation being an FDA Breakthrough Device for exosome depletion in cancer. In infectious disease, it competes with other broad-spectrum blood purification devices like ExThera's Seraph® 100, but targets a distinct viral indication.

Company Timeline

1999Founded

Founded in San Diego, United States

2003Series B

Series B: $10.0M

2005Series C

Series C: $15.0M

2006IPO

Initial Public Offering