- Aethlon Medical outlined its Hemopurifier platform, an extracorporeal blood filtration device designed to capture enveloped viruses and extracellular vesicles using an affinity resin.
- The company reported 173 treatments in 44 patients and said its clinical safety database shows a favorable safety profile.
- Aethlon Medical said it has two FDA Breakthrough Device designations covering advanced or metastatic cancer and life-threatening viral infections with no approved therapies.
- In its Australian oncology trial, the company said cohorts 1 and 2 are complete and cohort 3 is open for enrollment.
- Key financial highlights cited cash of about USD 7.0 million and about 1.6 million shares outstanding.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Aethlon Medical Inc. published the original content used to generate this news brief on March 27, 2026, and is solely responsible for the information contained therein.
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