Welcome to our dedicated page for Aethlon Medical news (Ticker: AEMD), a resource for investors and traders seeking the latest updates and insights on Aethlon Medical stock.
Aethlon Medical, Inc. (NASDAQ: AEMD) is a clinical-stage medical device innovator advancing the Hemopurifier® - a therapeutic filtration device targeting cancer-enabling exosomes and life-threatening viruses. This page provides investors and medical professionals with essential updates on clinical developments, regulatory progress, and strategic initiatives.
Key resources include press releases detailing trial protocols, ethics committee approvals, and operational milestones. Users will find verified information on oncology applications for treatment-resistant cancers and infectious disease programs, all presented in compliance with financial disclosure standards.
Content highlights encompass FDA communications, trial enrollment updates, and peer-reviewed research collaborations. The curated news collection serves as a reliable reference for tracking the Hemopurifier®'s progress through clinical validation stages and potential therapeutic applications.
Bookmark this page for direct access to Aethlon Medical's official announcements, including breakthrough device designations and international trial expansions. Check regularly for updates on this pioneering approach to blood filtration technology and its implications for cancer immunotherapy advancement.
Aethlon Medical (Nasdaq: AEMD) reported financials for the fiscal year ended March 31, 2022, revealing a cash balance of $17.1 million and a revenue of approximately $294,000, a decline from $659,000 in the prior year. Operating expenses rose to $10.72 million from $8.55 million, leading to a net loss of $10.4 million. The company is advancing the Hemopurifier for COVID-19 treatment and cancer, enrolling patients across multiple sites. Recent developments include ethics approval for a clinical trial in India and the appointment of Angela Rossetti to the Board.
Aethlon Medical, Inc. (Nasdaq: AEMD) will announce its financial results for the fiscal year ending March 31, 2022, on June 28, 2022, at 4:15 p.m. EST. A conference call will follow at 4:30 p.m. EST to discuss these results and recent corporate developments. The Hemopurifier, Aethlon's lead technology, is designed to treat cancer and infectious diseases, holding FDA Breakthrough Device designation for advanced cancer therapy and addressing life-threatening viruses. A replay of the conference will be available for a month post-call.
Aethlon Medical, Inc. (AEMD), a medical technology company, will present at the H.C. Wainwright Global Investment Conference from May 23-26, 2022, in Miami Beach, Florida, and virtually. The presentation, led by CEO Charles J. Fisher, Jr., CMO Steven LaRosa, and CFO James Frakes, will cover updates on the Hemopurifier®, a device aimed at treating cancer and viral infections. The presentation will be available on-demand starting May 24, 2022, at 7 a.m. EDT. The Hemopurifier® has received FDA designations as a Breakthrough Device for cancer and life-threatening viral infections, including COVID-19.
Aethlon Medical announced the publication of a pre-print manuscript showing its GNA affinity resin can capture seven SARS-CoV-2 variants, including Delta and Omicron, with efficiency rates between 53% and 89%. This resin is part of the Aethlon Hemopurifier®, an investigational device designed to remove viruses from the blood. The company is conducting an Early Feasibility Study on the Hemopurifier for COVID-19 patients. This research supports the potential effectiveness of the Hemopurifier against future variants, as stated by CEO Charles J. Fisher, Jr.
Aethlon Medical, Inc. (Nasdaq: AEMD) announced the appointment of Angela Rossetti to its Board of Directors, effective April 1, 2022. She replaces Sabrina Martucci Johnson, who steps down to focus on other roles. Rossetti brings over 20 years of biopharmaceutical experience, having held significant positions at various companies, including Pfizer. Her expertise in medical and clinical affairs is expected to boost the company's clinical advancements, particularly for the Hemopurifier, a device aimed at treating infectious diseases and cancer.
Aethlon Medical, Inc. (Nasdaq: AEMD) reported its financial results for the third quarter ending December 31, 2021. The company had a cash balance of approximately $20.4 million but recorded only $17,000 in revenue, a significant drop from $625,000 in the same period last year. Operating expenses decreased to $2.55 million, resulting in a net loss of about $2.5 million. Aethlon is advancing the Hemopurifier™ in clinical trials for Severe COVID and cancer, with progress made in patient enrollment across multiple sites.
Aethlon Medical, Inc. (Nasdaq: AEMD) will announce its financial results for Q3 FY2022, concluding on December 31, 2021, on February 14, 2022, at 4:15 p.m. EST. Management will hold a conference call at 4:30 p.m. EST to discuss these results and recent developments, followed by a Q&A session. The Hemopurifier, Aethlon's lead technology, is a FDA-designated Breakthrough Device aimed at treating advanced cancer and life-threatening infectious diseases. It has shown promising results in human studies, particularly in removing harmful viruses and exosomes from blood.
Aethlon Medical, Inc. (Nasdaq: AEMD) reported its financial results for the second quarter ended September 30, 2021, highlighting ongoing developments for the Hemopurifier™, a blood filtration system targeting COVID-19 and cancer. As of September 30, the company had $23.2 million in cash and generated $132,000 in government contract revenue, compared to none in the same quarter last year. Operating expenses rose to $2.1 million, resulting in a net loss of approximately $2.0 million. The company is advancing U.S. clinical trials and has expanded its international presence with a trial in India.
Aethlon Medical (AEMD) will announce its second quarter fiscal year 2022 financial results on November 9, 2021, at 4:15 p.m. EST. A conference call will follow at 4:30 p.m. EST, where management will discuss the financial results and corporate developments. The Hemopurifier, Aethlon's lead technology, targets life-threatening infections and cancer, and has received FDA Breakthrough Device designation. The company is conducting an Early Feasibility Study at the University of Pittsburgh to evaluate the Hemopurifier's effects on cancer-associated exosomes.