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) announced a pre-print manuscript detailing two case studies of critically ill COVID-19 patients treated with the Hemopurifier® via Emergency Use. The first patient showed recovery signs despite previous severe viremia and achieved hospital discharge after eight treatments. The second patient demonstrated the in vivo removal of SARS-CoV-2 but unfortunately expired due to disease severity. The company is conducting an Early Feasibility Study, aiming to enroll 40 ICU COVID-19 patients. The Hemopurifier is recognized as a Breakthrough Device for both cancer and life-threatening viral infections.
Aethlon Medical, Inc. (Nasdaq: AEMD) announced its participation in two virtual conferences: the H.C. Wainwright Global Life Sciences Virtual Conference on March 9-10, 2021, and the Maxim Group and M Vest 2021 Emerging Growth Virtual Conference on March 17-18, 2021.
The company’s presentations will include details on the Aethlon Hemopurifier, a device aimed at cancer treatment and viral infections, which holds FDA Breakthrough Device designation. Webcasts will be available on demand starting March 9 at 7:00 a.m. EST.
Aethlon Medical, Inc. (AEMD) reported its financial results for the third quarter ending December 31, 2020. The company had a cash balance of $12.1 million, with government contract revenue increasing to approximately $625,000 from $413,000 year-over-year. Operating expenses surged by 137.9% to $3.07 million, largely due to payroll increases from severance costs and clinical trial expenses. Consequently, the net loss rose to about $2.44 million compared to $821,000 in the same quarter last year. Aethlon continues to develop its Hemopurifier and has initiated clinical trials for COVID-19 and cancer treatments.
Aethlon Medical, Inc. (Nasdaq: AEMD) will release its third quarter fiscal year 2021 financial results on February 10, 2021, at 4:15 p.m. EST. Management will host a conference call at 4:30 p.m. EST to review the results and discuss corporate developments. The Hemopurifier®, Aethlon's immunotherapeutic device, targets cancer and viral infections and has received FDA Breakthrough Device designations. Notably, it is currently being evaluated in a feasibility study for treating COVID-19 patients. Interested parties can register or dial in for the call.
Aethlon Medical, Inc. (Nasdaq: AEMD) announced key executive appointments on January 6, 2021, enhancing its leadership team. Guy Cipriani joins as Senior Vice President and Chief Business Officer, focusing on business development and fundraising, while Dr. Steven LaRosa becomes Chief Medical Officer, overseeing clinical operations for the Hemopurifier®. Cipriani's extensive background includes significant roles at Microbion and Cardiome Pharma, while LaRosa has clinical experience in infectious diseases. The Hemopurifier, an FDA-designated 'Breakthrough Device,' aims to address cancer and severe viral infections.
Aethlon Medical, Inc. (Nasdaq: AEMD) will present at the virtual H.C. Wainwright BioConnect 2021 Conference from Jan. 11-14, 2021. A webcast of their presentation will be available on-demand starting at 6:00 a.m. EDT on Jan. 11, accessible through their website. The company focuses on addressing unmet needs in viral diseases and cancer with its Hemopurifier device, designated as a Breakthrough Device by the FDA. It aims to combat cancer by depleting tumor-derived exosomes and has received FDA approval for an Early Feasibility Study for COVID-19 treatment.
Aethlon Medical, Inc. (AEMD) has announced the treatment of its first patient in a first-in-human Early Feasibility Study (EFS) using the HEMOPURIFIER® for patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck at UPMC Hillman Cancer Center, Pittsburgh. The trial aims to assess the safety of the HEMOPURIFIER® and its potential to improve the efficacy of pembrolizumab (KEYTRUDA®) by reducing cancer-associated exosomes. This represents a crucial step in addressing unmet needs in cancer treatment, especially regarding immune suppression caused by tumor-derived exosomes.
Aethlon Medical, Inc. (Nasdaq: AEMD) appointed Dr. Charles J. Fisher, Jr. as CEO effective October 30, 2020, succeeding Dr. Timothy Rodell, who will transition to a consultancy role. Dr. Fisher has significant experience, including leadership roles at Eli Lilly and Abbott Laboratories, and is expected to enhance Aethlon's product development, particularly the Hemopurifier, aimed at treating life-threatening viral infections and cancer. The company is now initiating clinical trials for the Hemopurifier in patients with COVID-19 and advanced cancer.
Aethlon Medical, Inc. (AEMD) reported its financial results for the second quarter ending September 30, 2020. The company has approximately $14.5 million in cash and reported a net loss of about $1.77 million, up from $1.71 million year-over-year. Operating expenses increased by 4.1% to $1.77 million, driven by higher general and administrative costs.
The company is advancing its Hemopurifier device through FDA-approved clinical trials for cancer and COVID-19 treatments. The first trial is open for enrollment in patients with advanced head and neck cancer.
Aethlon Medical, Inc. (AEMD) will release its financial results for Q2 FY2021 on October 28, 2020, at 4:15 PM ET. The results will cover the period ending September 30, 2020. A conference call will follow at 4:30 PM ET, allowing management to discuss the outcomes and recent developments. Interested participants can register online for the conference call or dial in using the toll-free or international numbers provided. Aethlon focuses on unmet health needs, particularly with its Aethlon Hemopurifier®, a device for treating cancer and viral infections.
