Welcome to our dedicated page for Aim Immunotech news (Ticker: AIM), a resource for investors and traders seeking the latest updates and insights on Aim Immunotech stock.
AIM ImmunoTech Inc. (NYSE American: AIM) is a pioneering immuno-pharma company based in Ocala, Florida, focused on the research and development of innovative therapeutics aimed at treating a variety of cancers, immune disorders, and viral diseases including COVID-19. The company's flagship product is Ampligen® (rintatolimod), a first-in-class investigational drug that acts as a highly selective TLR3 agonist immuno-modulator with broad-spectrum activity. Ampligen is currently undergoing extensive clinical trials targeting globally important cancers and viral diseases.
AIM ImmunoTech's product portfolio also includes Alferon N Injection, an injectable formulation of natural alpha interferon used to treat a specific category of genital warts, a sexually transmitted disease. Ampligen has shown promising results in the treatment of chronic fatigue syndrome and is being developed for other indications like hepatitis B, HIV, and several cancer types, including renal cell carcinoma, malignant melanoma, non-small cell lung cancer, ovarian cancer, breast cancer, colorectal cancer, urothelial cancer, prostate cancer, and pancreatic cancer.
In recent developments, AIM ImmunoTech announced positive top-line interim data indicating that the combination of Ampligen with Keytruda (pembrolizumab) could be significantly more effective than pembrolizumab alone in treating recurrent ovarian cancer. The company is also working on various clinical trials, including studies for treating post-COVID conditions and long COVID, led by renowned medical experts like Dr. Charles Lapp.
AIM ImmunoTech has formed strategic research agreements with prominent institutions such as the Japanese National Institute of Infectious Diseases and Shionogi & Co., Ltd., exploring the potential of Ampligen as an adjuvant therapy for COVID-19. The company continues to focus on operational execution and has successfully completed cGMP manufacturing of over 9,000 clinical vials of Ampligen, which is crucial for its ongoing and upcoming clinical trials.
The company's leadership team, headed by CEO Thomas K. Equels, is committed to advancing its pipeline and achieving clinical and commercial success. AIM ImmunoTech engages with its stakeholders through regular updates and CEO Corner segments, providing insights into its clinical programs and financial performance, ensuring transparency and fostering investor confidence.
For more detailed information, visit the official website and connect with AIM ImmunoTech on social media platforms such as X, LinkedIn, and Facebook.
AIM ImmunoTech Inc. announced the issuance of Patent No. 2027383 by the Netherlands Patent Office, covering Ampligen (rintatolimod) and related products for treating COVID-19, with patent protection extending until 2041. The patent supports AIM’s ongoing research programs in the Netherlands to combat various cancers, immune disorders, and viral diseases. The company has filed multiple patent applications covering Ampligen, enhanced immunity against COVID-19 variants, and is progressing towards filing an IND application for a Phase 2 study addressing Long COVID conditions.
AIM ImmunoTech Inc. (NYSE: AIM) announced that CEO Thomas K. Equels will present at the H.C. Wainwright Global Investment Conference from May 23-26, 2022, in Miami, FL, and virtually. The company focuses on developing therapeutics for cancer, immune disorders, and viral diseases, including COVID-19. A video webcast of the presentation will be available on-demand starting May 24, 2022. AIM's lead product, Ampligen®, is in clinical trials for various cancers and is approved for treatment of ME/CFS in Argentina.
AIM ImmunoTech Inc. (NYSE: AIM) announced progress in its research on Ampligen, aimed at treating Long COVID and Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). A Phase 3 trial indicated a 51.2% positive response in patients with early ME/CFS symptoms. Following promising results from an expanded access program, AIM plans to file an Investigational New Drug application for a Phase 2 study of Ampligen. Experts express optimism about Ampligen's potential benefits for Long COVID patients, highlighting the urgency for effective therapeutics.
AIM ImmunoTech Inc. (NYSE: AIM) reported significant clinical advancements in the first quarter of 2022, showcasing Ampligen's efficacy in late-stage pancreatic cancer, ovarian cancer, and triple-negative breast cancer. The company is on track to begin a Phase 2 study for Ampligen in pancreatic cancer by Q3 2022. AIM also holds a robust cash position of $44.5 million, expected to support operations through 2023. The FDA has lifted the clinical hold on its IND application, allowing further studies to proceed.
AIM ImmunoTech Inc. (NYSE: AIM) announced participation in the Solve M.E. Diagnostics event on May 19, 2022, focusing on Long COVID and its implications. CEO Thomas K. Equels will discuss the clinical development of Ampligen for treating ME/CFS and Long COVID. Ampligen, AIM's RNA product candidate, is designed to modulate the immune system and has shown anti-viral properties. The company sponsors an expanded access program for ME/CFS patients in the U.S., having dosed its first Long Hauler patient in this initiative in 2021.
AIM ImmunoTech Inc. (AIM) reported promising results from clinical studies involving Ampligen, an anti-tumor drug with potential synergy when combined with PD-1 and PD-L1 checkpoint inhibitors. Ampligen shows efficacy in treating triple-negative breast cancer and advanced recurrent ovarian cancer, as evidenced by significant survival rates in pre-clinical and human studies. The company aims to expand Ampligen's application to solid tumors based on emerging clinical data. Key findings include increased immune response markers and indications of tumor microenvironment reprogramming that could enhance treatment outcomes.
AIM ImmunoTech Inc. announced promising results for Ampligen® (rintatolimod) as a potential maintenance therapy for advanced pancreatic cancer. Following FDA clearance, AIM will commence a Phase 2 study (AMP-270) in Q3 2022, comparing Ampligen to a no-treatment control after FOLFIRINOX chemotherapy. The trial will enroll around 90 patients at multiple sites in the U.S. and Europe. Recent data showed improved median survival times for patients treated with Ampligen compared to historical controls, indicating its potential effectiveness in this challenging indication.
AIM ImmunoTech announced positive results from a Phase 1 study on metastatic triple-negative breast cancer (mTNBC), utilizing chemokine modulation therapy with Ampligen and pembrolizumab. The trial met its primary endpoint by enhancing cytotoxic T-lymphocyte infiltration in the tumor microenvironment. Results indicated significant disease stabilization in three out of six patients and impressive immune marker increases, suggesting potential efficacy. The data was presented at the AACR Annual Meeting 2022.
AIM ImmunoTech Inc. (AIM) announced positive results from its Phase 2a clinical study on Ampligen for treating colorectal cancer metastatic to the liver. The primary endpoint was achieved with a significant increase in CD8a expression post-treatment (p=0.046), suggesting that the CKM regimen may enhance immunotherapy effectiveness. Data presented at the AACR 2022 showed improved ratios of CD8a/CD4 and CD8a/FOXP3, indicating a favorable immune response. The median overall survival was 10.5 months. However, no tumor responses were observed, and adverse events were reported in 74% of participants.
AIM ImmunoTech reported its 2021 financial results, noting significant progress in its oncology pipeline and Ampligen® data demonstrating efficacy across various cancer treatments. The FDA lifted the clinical hold on Ampligen's Phase 2 study for pancreatic cancer, allowing advanced trials to proceed. AIM has a strong cash position of $48.3 million as of December 31, 2021, and expects to maintain operations and clinical programs through 2023. The company aims to leverage upcoming clinical and regulatory milestones in 2022 to drive further growth.