AEMD (.47) trying to break the 52-wk high. This will move much higher by next week on anticipated breakthrough news in HCV!
Best, $heff
Aethlon Medical (AEMD.OB) is developing the Hemopurifier filter cartridge as a potentially new and additive treatment for chronic infection with the hepatitis C virus (HCV), in addition to other viral infections (HIV, influenza-pandemic flu), bio-terror agents, and cancer. The Company's filter technology platform combines principles of both dialysis and affinity chromatography to selectively remove unwanted substances from the blood (e.g. viruses) with a coating of a plant protein called a lectin that binds to specific carbohydrate molecules on the surface of some cell membranes which are not normally present in humans.
To conduct human studies in the U.S., AEMD.OB must receive approval from the FDA based on the Company's Investigational Device Exemption (IDE) application, which must be amended for the Company's proposed use in HCV therapy. The Company hopes to schedule a meeting with the FDA during Fall 2009 (11/15/09 is just an estimate for this entry) based on study data generated in India that includes two small clinical trials demonstrating the ability for the Hemopurifier to bind/remove HCV from the blood of infected patients. This data will be presented at the ASN Conference on Oct. 30th.
From BioMedReports.com
AEMD.OB has completed safety and efficacy studies including 12 collaborative in-vitro studies, animal studies, and human studies. In addition, the Company has conducted five years of research + proof of principle studies on the Hemopurifier and is moving towards commercialization on a named-patient basis in India.
Best, $heff
Aethlon Medical (AEMD.OB) is developing the Hemopurifier filter cartridge as a potentially new and additive treatment for chronic infection with the hepatitis C virus (HCV), in addition to other viral infections (HIV, influenza-pandemic flu), bio-terror agents, and cancer. The Company's filter technology platform combines principles of both dialysis and affinity chromatography to selectively remove unwanted substances from the blood (e.g. viruses) with a coating of a plant protein called a lectin that binds to specific carbohydrate molecules on the surface of some cell membranes which are not normally present in humans.
To conduct human studies in the U.S., AEMD.OB must receive approval from the FDA based on the Company's Investigational Device Exemption (IDE) application, which must be amended for the Company's proposed use in HCV therapy. The Company hopes to schedule a meeting with the FDA during Fall 2009 (11/15/09 is just an estimate for this entry) based on study data generated in India that includes two small clinical trials demonstrating the ability for the Hemopurifier to bind/remove HCV from the blood of infected patients. This data will be presented at the ASN Conference on Oct. 30th.
From BioMedReports.com
AEMD.OB has completed safety and efficacy studies including 12 collaborative in-vitro studies, animal studies, and human studies. In addition, the Company has conducted five years of research + proof of principle studies on the Hemopurifier and is moving towards commercialization on a named-patient basis in India.
Recent AEMD News
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:10 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:09 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:08 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/21/2026 09:00:06 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/01/2026 11:27:48 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/01/2026 11:27:34 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/01/2026 11:27:18 PM
- Advancements in Novel Immunotherapeutics in The Oncology Battle • Newsfile • 03/24/2026 02:30:00 PM
- Aethlon Medical, Inc. Advances to Final Cohort in Oncology Clinical Trial Following Positive DSMB Review • PR Newswire (US) • 03/24/2026 12:01:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/17/2026 01:15:09 PM
- Life Sciences Virtual Investor Forum Presentations Now Available for Online Viewing • GlobeNewswire Inc. • 03/13/2026 12:35:00 PM
- Aethlon Medical Engages Maxim Group LLC to Evaluate Strategic Opportunities • PR Newswire (US) • 03/12/2026 12:01:00 PM
- Life Sciences Virtual Investor Forum Agenda Announced for March 11th & 12th • GlobeNewswire Inc. • 03/10/2026 02:21:44 PM
- Aethlon Medical to Present at the Life Sciences Investor Forum on March 12th • GlobeNewswire Inc. • 03/06/2026 01:35:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/23/2026 09:15:32 PM
- Form SCHEDULE 13G - Statement of Beneficial Ownership by Certain Investors • Edgar (US Regulatory) • 02/18/2026 02:54:05 AM
- Form SCHEDULE 13G/A - Statement of Beneficial Ownership by Certain Investors: [Amend] • Edgar (US Regulatory) • 02/18/2026 01:22:47 AM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/12/2026 10:10:41 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/12/2026 09:15:44 PM
- Aethlon Medical Announces Fiscal Q3 2026 Financial Results and Corporate Update • PR Newswire (US) • 02/12/2026 09:15:00 PM
- Aethlon Medical to Release Fiscal Third Quarter Financial Results and Host Conference Call on February 12, 2026 • PR Newswire (US) • 02/04/2026 01:01:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 01/27/2026 09:15:36 PM
- Form DEFA14A - Additional definitive proxy soliciting materials and Rule 14(a)(12) material • Edgar (US Regulatory) • 01/27/2026 09:15:26 PM

