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Aethlon Medical (AEMD) investor relations material
Aethlon Medical Registration Filing summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Company overview and business model
Focuses on developing the Hemopurifier, a clinical-stage immunotherapeutic device targeting cancer, life-threatening viral infections, and organ transplantation applications.
Hemopurifier uses proprietary lectin-based technology to remove harmful exosomes and viral particles from biological fluids.
FDA has designated the Hemopurifier as a Breakthrough Device for advanced/metastatic cancer and life-threatening viruses not addressed by approved therapies.
Ongoing clinical trials in Australia and India for oncology indications; prior studies in HIV, hepatitis C, Ebola, and COVID-19.
No current sales or marketing capability; future commercialization plans include building or contracting distribution and sales.
Financial performance and metrics
Research and development expenses were $2,212,000 and $2,520,000 for fiscal years ended March 31, 2025 and 2024, respectively.
For the six months ended September 30, 2025 and 2024, R&D expenses were $818,686 and $702,115, respectively.
As of December 18, 2025, 971,872 shares of common stock were outstanding.
Net tangible book value as of September 30, 2025 was $6.95 per share; after the offering, as adjusted, $4.86 per share.
Use of proceeds and capital allocation
Net proceeds intended for general corporate purposes, including R&D, administrative expenses, working capital, and capital expenditures.
May use proceeds for debt repayment, refinancing, or acquisitions, but no current commitments.
Management has broad discretion over allocation of proceeds.
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