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Aethlon Medical Inc. (Nasdaq: AEMD) is an innovative medical technology company dedicated to addressing unmet medical needs in health and biodefense. The company's core focus is on developing the Hemopurifier®, a clinical-stage therapeutic device designed to combat cancer and life-threatening viral infections, and for use in organ transplantation. Aethlon’s proprietary technology, the Aethlon ADAPT™ platform, provides the foundation for a new class of therapeutics that target the selective removal of disease-enabling particles from the entire circulatory system.
The Hemopurifier®, designated as a breakthrough device by the FDA, has demonstrated broad-spectrum capabilities against exosomes that contribute to the progression of cancer and viruses like HIV and Hepatitis C. Recent developments include ongoing research and clinical trials to evaluate the device's safety and efficacy in removing harmful exosomes and viruses from blood. These trials are taking place in India and Australia, targeting patients with solid tumors who have stable or progressive disease during anti-PD-1 monotherapy treatment, such as Keytruda® or Opdivo®.
Financially, Aethlon Medical reported a cash balance of approximately $8.0 million as of the end of 2023. The company also announced a public offering expected to raise around $4.7 million to support its clinical trials, research, and other corporate needs. The company's leadership, including Interim CEO and CFO Jim Frakes, is committed to advancing the Hemopurifier® and exploring new applications in oncology and infectious diseases.
Partnerships are a crucial aspect of Aethlon’s strategy. The company recently entered into a Materials Transfer Agreement with Santersus AG to explore potential synergies between the Hemopurifier® and Santersus' NucleoCapture devices for the treatment of cancer and organ transplantation. This collaboration aims to enhance the effectiveness of both technologies by combining their capabilities to remove specific harmful agents from the blood.
Overall, Aethlon Medical Inc. is at the forefront of developing groundbreaking medical devices aimed at improving outcomes for patients with severe health conditions, making significant strides in the fields of cancer and infectious diseases.
For more information, visit Aethlon Medical.
The solid tumors market is expected to reach $375.4 Billion by 2034, with a CAGR of 7.45% from 2024-2034. Aethlon Medical (NASDAQ: AEMD) has activated a clinical trial site at Royal Adelaide Hospital for its Hemopurifier device in patients with solid tumors resistant to anti-PD-1 therapies. The trial aims to assess safety, feasibility, and dosing, with potential to improve response rates to immunotherapies by removing tumor-produced extracellular vesicles.
Other developments in the solid tumor space include Immuneering's positive initial data for IMM-1-104 in pancreatic cancer, and FDA approvals for new immunotherapy combinations from AstraZeneca, Merck, and GlaxoSmithKline for endometrial cancer. Roche's trastuzumab deruxtecan received accelerated approval for HER2-positive solid tumors across multiple cancer types.
Aethlon Medical (Nasdaq: AEMD) has announced the activation of the Cancer Clinical Trial Unit at Royal Adelaide Hospital to begin screening and enrolling patients for its Hemopurifier® clinical trial. The trial, focusing on patients with solid tumors not responding to anti-PD-1 antibodies, aims to assess safety, feasibility, and dosing of the Hemopurifier®.
Key points:
- Trial activation date: September 10, 2024
- Led by Prof. Michael Brown at Royal Adelaide Hospital, Australia
- Approximately 18 patients expected to participate
- Primary endpoint: Incidence of adverse events and safety lab changes
- Hemopurifier® designed to remove tumor-produced extracellular vesicles (EVs)
- Potential to improve response rates to anti-PD-1 therapies
Aethlon Medical (Nasdaq: AEMD) has published a preclinical study demonstrating the ability of its Hemopurifier® to remove extracellular vesicles (EVs) and microRNAs from renal perfusates following Controlled Oxygenated Rewarming of discarded donor kidneys. The study, published in bioRxiv on August 24, 2024, supports further research into using the Hemopurifier® as part of a machine perfusion circuit to assess its impact on retrieved kidney function.
The proof-of-concept study used four perfusates from discarded donor kidneys, confirming the removal of both small and larger size EVs and a significant reduction in microRNAs. This research could potentially address complications associated with extended criteria donor kidneys, which often result in poor graft function and acute rejection in recipients.
Aethlon Medical (AEMD) reported financial results for Q1 FY2025 ended June 30, 2024. Key highlights:
1. Received ethics approvals for Hemopurifier® trial in Australia for solid tumor patients not responding to anti-PD-1 antibodies.
2. Expects to open patient enrollment in October 2024.
3. Achieved 24% reduction in Q1 operating expenses vs. Q1 FY2024.
4. Cash balance of $9.1 million as of June 30, 2024.
5. Net loss decreased to $2.6 million in Q1 FY2025 from $3.3 million in Q1 FY2024.
6. Exploring Hemopurifier use for viral infections.
7. COVID-19 trial in India remains open.
Aethlon Medical, Inc. (NASDAQ: AEMD) has received ethics approval for a clinical trial of its Hemopurifier® device in patients with solid tumors. The trial, to be conducted at Pindara Private Hospital in Australia, will evaluate the safety and feasibility of the Hemopurifier® in patients with stable or progressive disease during anti-PD-1 monotherapy treatment.
The Hemopurifier® is designed to remove harmful exosomes from biological fluids, which may improve therapeutic response rates to anti-PD-1 antibodies. The device has shown promise in preclinical studies for reducing exosomes in cancer patient plasma samples.
This development comes as the solid tumor therapeutics market is projected to reach $885.44 Billion by 2033, with smaller companies making significant advancements in treatments alongside big pharma.
Aethlon Medical (NASDAQ: AEMD) has received full ethics approval from the Bellberry Human Research Ethics Committee for a clinical trial of its Hemopurifier® at Pindara Private Hospital in Queensland, Australia. The trial will study the safety, feasibility, and dosing of the Hemopurifier in patients with solid tumors not responding to anti-PD-1 antibodies like Keytruda® or Opdivo®. This is the second ethics approval for the oncology trial in Australia, following approval at Royal Adelaide Hospital in June.
The trial aims to enroll 9-18 patients and will focus on safety as the primary endpoint. It will also explore the Hemopurifier's ability to reduce extracellular vesicles (EVs) in cancer patients' blood, which may improve response rates to anti-PD-1 therapies. The study results are expected to inform the design of a future Premarket Approval (PMA) study.
Aethlon Medical (Nasdaq: AEMD), a medical therapeutic company developing products for cancer and infectious diseases, has announced its fiscal first quarter financial results release and conference call for August 14, 2024. The company will issue financial results for the quarter ended June 30, 2024, at 4:15 p.m. ET, followed by a conference call at 4:30 p.m. ET. Management will review financial results and recent corporate developments, with a subsequent Q&A session. Interested parties can register online or dial in directly. A replay will be available until September 14, 2024, accessible via Aethlon's website or by phone.
Aethlon Medical (Nasdaq: AEMD) announced financial results for the fiscal year ending March 31, 2024, and provided a corporate update. The company continues the clinical development of its Hemopurifier® for cancer and infectious diseases, receiving ethics approval for a clinical trial in Australia. Financially, Aethlon reported a net loss of $12.2 million, a slight increase from the previous year's $12 million. Operating expenses rose marginally to $12.6 million from $12.5 million, driven by increased payroll costs. The current cash balance stands at $9.1 million. Efforts are ongoing to secure approvals for additional trial sites in Australia and India, with patient enrollment expected by late 2024.
Aethlon Medical (Nasdaq: AEMD) will release its fiscal year-end financial results on June 27, 2024, at 4:15 p.m. ET. The company focuses on developing therapeutic products for cancer and serious infectious diseases.
Management will host a conference call the same day at 4:30 p.m. ET to discuss the financial results and recent corporate developments. The call will include a Q&A session.
Participants can register for the call at https://dpregister.com/sreg/10190237/fce977aef1, where they will receive dial-in numbers. Those without internet access can dial in toll-free at 1-844-836-8741 or internationally at 1-412-317-5442.
A replay of the call will be available until July 27, 2024, via Aethlon Medical's website or by dialing 1-877-344-7529 (domestic) or 1-412-317-0088 (international), using replay conference ID 6876352.
Investorideas.com has released an industry snapshot on the future treatment of solid cancer tumors, highlighting Aethlon Medical's (NASDAQ: AEMD) advancements. Aethlon announced the Human Research Ethics Committee's approval for a clinical trial of its Hemopurifier in cancer patients with stable or progressive disease during anti-PD-1 therapy, valid until June 2027. This trial aims to improve responses to treatments like Keytruda and Opdivo by removing extracellular vesicles from the bloodstream. The Hemopurifier has shown promise in preclinical studies, reducing exosomes in cancer patient samples. The trial, led by Prof. Michael Brown in Adelaide, Australia, will evaluate safety and treatment efficacy over two months. The market for solid tumor therapeutics is projected to grow from USD 222.71 billion in 2023 to USD 885.44 billion within ten years, driven by increased R&D investments. Key developments include AbbVie's acquisition of ImmunoGen and significant advancements in their antibody-drug conjugate platform.
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