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A e thlon Medical, Inc . Nasdaq : AEMD BIO International Convention San Francisco

Key Takeaway: A e thlon Medical, Inc . Nasdaq : AEMD BIO International Convention San Francisco June 7, 2016 Jim Joyce Chairman, CEO FORWARD LOOKING STATEMENTS The following presentation may contain predictions, estimates, and other forward looking statements that involve risks and uncertaint

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A e thlon Medical, Inc . Nasdaq : AEMD BIO International Convention San Francisco June 7, 2016 Jim Joyce Chairman, CEO
FORWARD LOOKING STATEMENTS The following presentation may contain predictions, estimates, and other forward looking statements that involve risks and uncertainties, including whether and when our products are successfully developed and introduced ; market acceptance of the A e thlon ADAPT and ELLSA platform technologies, the H e mopurifier and other product offerings ; regulatory delays, manufacturing delays, and other risks detailed in our SEC filings, which are accessible at www . sec . gov or on our website : www . A e thlonMedical . com
IMMUNOTHERAPEUTIC TECHNOLOGIES TO COMBAT INFECTIOUS DISEASE & CANCER
Summary Clinical - stage Company Lead therapeutic - The Aethlon Hemopurifier - B road - spectrum countermeasure against emerging pandemic threats - Discovered to capture cancer - promoting exosomes Significant unmet need in cancer care Exosome Sciences, Inc. (diagnostic subsidiary) - ELLSA exosome isolation platform (virus & cancer) - Discovered a candidate biomarker to diagnose CTE
The A e thlon Hemopurifier Broad - s pectrum e limination of circulating viruses, viral particles and bacterial toxins
DEPLOYED WITHIN THE GLOBAL INFRASTRUCTURE OF DIALYSIS & CRRT MACHINES
The Hemopurifier Mechanism of Action Rapid separation of disease targets from the circulatory blood path Capture of disease targets through adherence to surface structure that provides immune - evasion - Lectin - affinity attachment to high - mannose signature that cloaks pathogen targets from immune surveillance
The Hemopurifier establishes a therapeutic strategy to address the hundreds of viruses that are not treatable with antiviral drug agents .
The A e thlon Hemopurifier FDA approved IDE study currently being conducted
Previous Human Treatment Experiences
BROAD - SPECTRUM HUMAN TREATMENT EXPERIENCES HIV - AIDS Hepatitis - C Ebola
The Treatment of Ebola Virus Frankfurt University Hospital Special approval from The Federal Institute for Drugs and Medical Devices (BfArM)
Hemopurifier therapy administration to a comatose Ebola patient with multiple - organ failure
Dr. Stefan B ttner Holding Hemopurifier After Ebola Treatment
Ebola Treatment Data Presented By Dr. Helmut Geiger American Society of Nephrology Annual Meeting 6.5 hour Hemopurifier therapy administration Pre - treatment viral load: 400,000 copies/ml Post - treatment viral load: 1,000 copies/ml Patient recovered and returned home
Extracorporeal Virus Elimination for the Treatment of Severe Ebola Virus Disease - First Experience with Lectin Affinity Plasmapheresis Stefan Bu ttner a Benjamin Koch a Olga Dolnik b Markus Eickmann b Tilo Freiwald a Sarah Rudolf a Ju rgen Engel a Stephan Becker b Claudio Ronco c Helmut Geiger a a Medical Clinic III, Department of Nephrology, University Hospital Frankfurt, Frankfurt am Main, and b Institute of Virology, Philipps University Marburg, Marburg, Germany; c Department of Nephrology, Dialysis and Transplantation, International Renal Research Institute of Vicenza (IRRIV), San Bortolo Hospital, Vicenza, Italy Published: Journal of Blood Purification
"Top 25 Best Inventions" "11 Most Remarkable Advances in Healthcare"
Pre - clinical Validations ( Reported t o date )
In Vitro Hemopurifier Validations Viruses - Hepatitis C, HIV, Ebola, H1N1 Swine Flu, H5N1 Bird Flu, 1918 Spanish Flu (reconstructed), Monkey Pox, West Nile Virus, Chikungunya and Dengue Viral Toxins Ebola glycoprotein ( gp ), HIV gp120, HIV NEF - exosomes Bacterial Toxins L ipopolysaccharide (LPS) and L ipoteichoic acid (LTA) Tumor - derived E xosomes
Initiated tumor - derived exosome research in 2006 Considered c ellular debris w ith n o b iological f unction CANCER
2016 Tumor - derived exosomes are significant therapeutic and diagnostic targets
Tumor - Derived Exosomes
Tumor - Derived Exosomes A Significant Unmet Medical Need in Cancer The seeds of cancer metastasis - Metastasis contributes to 90% of cancer deaths - The mystery of the Soil & Seed Theory of 1889 Tumor - derived exosomes promote: - Tumorigenesis - Cancer progression - Angiogenesis - Immune - evasion - Resistance to radiation and chemotherapeutic drugs
The Hemopurifier provides an adjunct strategy to optimize emerging immuno - oncology drugs or improve the benefit of chemotherapeutic regimens
ELLSA (Enzyme - linked lectin - specific assay) Proprietary exosome isolation platform
ELLSA Isolates disease - origin exosomes from bodily fluids - ELLSA step + specific antibody step to diagnose and monitor a variety of disease indications - Urine based proof - of - principal established in HIV Identified HIV - specific exosomes in 111 HIV - infected individuals, but not in the urine of 35 HIV negative control subjects. A potential noninvasive global strategy to diagnose HIV infection. In collaboration with Morehouse School of Medicine, who conducted the study
Chronic Traumatic Encephalopathy (CTE)
Discovery of CTE biomarker candidate ( TauSome ) TauSome testing was conducted in the DETECT study - In collaboration with the Boston University CTE Center Principal Investigator: Robert Stern Ph.D. - Goal: a test that could detect CTE in living individuals - 78 former NFL players (high risk CTE group) - 16 athlete controls (low risk CTE group)
Preliminary Study of Plasma Exosomal Tau as a Potential Biomarker for Chronic Traumatic Encephalopathy Stern , Tripodis , Baugh, Fritts , Martin, Chaisson , Cantu, Joyce, Shah, Ikezu , Zhang, Gercel - Taylor, & Taylor J Alzheimer's Disease, 2016 Findings suggest that TauSome plasma levels may be an accurate, noninvasive CTE biomarker - TauSome levels significantly higher in the NFL group - TauSome levels correlated with cognitive decline
0 2 4 6 8 10 12 14 16 18 1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 31 33 35 37 39 41 43 45 47 49 51 53 55 57 59 61 63 65 67 69 71 73 75 77 79 81 83 85 87 89 91 93 TauSome Concentration (x10 9 /mL) Patient Samples *Horizontal lines represent average TauSome concentration for each group. Control Samples - n=16 - Avg : 310,000,000 TauSomes /mL - SD: 1.9 E8 NFL Player Samples - n=78 - Avg : 2,800,000,000 TauSomes /mL - SD: 2.9 E9
TauSome Next Steps (more testing required) - Validate that TauSomes are brain - derived - Refine technique to ELLSA - antibody or other scalable methodology - Initiate TauSome studies in other tauopathies - Initiate TauSome studies in other high - risk CTE groups - TauSome testing to be included in new (up to a 17 - sites) CTE study funded by a $ 16 million NIH grant
Summary Clinical - stage Company Lead therapeutic - The Aethlon Hemopurifier - B road - spectrum countermeasure against emerging pandemic threats - Discovered to capture cancer - promoting exosomes Significant unmet need in cancer care Exosome Sciences, Inc. (diagnostic subsidiary) - ELLSA exosome isolation platform (virus & cancer) - Discovered a candidate biomarker to diagnose CTE
IMMUNOTHERAPEUTIC TECHNOLOGIES TO COMBAT INFECTIOUS DISEASE & CANCER
Acknowledgement and Thanks Team Aethlon Battelle Memorial Research Institute Boston University CTE Center DaVita Med Center Dialysis Defense Advanced Research Projects Agency (DARPA ) Frankfurt University Hospital Medanta Medicity , Fortis and Apollo Hospitals Morehouse School of Medicine National Institute of Virology (NIV) Pune, India Philipps University Marburg U.S. Army Medical Research Institute for Infectious Diseases (USAMRIID ) U.S. Centers for Disease Control (CDC)
CONTACT: A e thlon Medical, Inc 9635 Granite Ridge Drive Suite 100 San Diego, California 92123 Jim Joyce Chairman & CEO jj@aethlonmedical.com 858.459.7800 x301
Last updated: Jun 7, 2016