Altamira Therapeutics .(CYTO)
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Altamira Therapeutics Announces Closing of up to $12.0 Million Public Offering
GlobeNewswire News Room· 2024-09-19 20:01
Core Viewpoint - Altamira Therapeutics Ltd. has successfully closed a public offering, raising approximately $4 million, with potential additional proceeds of up to $8 million from milestone-linked warrants [1][3]. Group 1: Offering Details - The public offering consisted of 5,555,556 common shares at a price of $0.72 per share, along with Series A-1 and Series A-2 common warrants [1]. - Series A-1 common warrants have an exercise price of $0.72, are immediately exercisable, and expire either 18 months after issuance or 60 days after positive biodistribution data is announced [1]. - Series A-2 common warrants also have an exercise price of $0.72, are immediately exercisable, and expire either five years after issuance or six months after entering into development agreements for AM-401 or AM-411 [1]. Group 2: Financial Implications - The gross proceeds from the offering were approximately $4 million before deducting fees and expenses, with potential additional proceeds of about $8 million if all warrants are exercised [3]. - The net proceeds from the offering will be used for working capital and general corporate purposes [3]. Group 3: Company Background - Altamira Therapeutics is focused on developing RNA delivery technology for targets beyond the liver, with two flagship siRNA programs, AM-401 for KRAS-driven cancer and AM-411 for rheumatoid arthritis, currently in preclinical development [7]. - The company also holds a 49% stake in Altamira Medica AG, which markets Bentrio®, an OTC nasal spray for allergic rhinitis [7]. - Founded in 2003, Altamira is headquartered in Hamilton, Bermuda, with operations in Basel, Switzerland [8].
Altamira Therapeutics Announces Pricing of up to $12.0 Million Public Offering
GlobeNewswire News Room· 2024-09-17 21:00
Core Viewpoint - Altamira Therapeutics Ltd. has announced a public offering of common shares and warrants, aiming to raise approximately $4 million upfront, with potential additional proceeds of up to $8 million from the exercise of warrants [1][3]. Group 1: Offering Details - The public offering includes 5,555,556 common shares priced at $0.72 each, along with Series A-1 and Series A-2 common warrants, each allowing the purchase of an equal number of shares at the same price [1]. - The Series A-1 warrants will expire either 18 months after issuance or 60 days after positive biodistribution data is announced for AM-401 or AM-411 [1]. - The Series A-2 warrants will expire either five years after issuance or six months after entering agreements for further development and commercialization of AM-401 or AM-411 [1]. Group 2: Financial Proceeds and Use - The expected gross proceeds from the offering are approximately $4 million before fees and expenses, with an additional potential $8 million if all warrants are exercised [3]. - The net proceeds from the offering will be used for working capital and general corporate purposes [3]. Group 3: Company Background - Altamira Therapeutics is focused on developing RNA delivery technology for targets beyond the liver, with two flagship siRNA programs, AM-401 for KRAS-driven cancer and AM-411 for rheumatoid arthritis, currently in preclinical development [7]. - The company also holds a 49% stake in Altamira Medica AG, which markets Bentrio®, an OTC nasal spray for allergic rhinitis [8]. - Founded in 2003, Altamira is headquartered in Hamilton, Bermuda, with operations in Basel, Switzerland [8].
REPEAT -- Diamond Equity Research Releases Update Note on Altamira Therapeutics Ltd. (NASDAQ: CYTO)
GlobeNewswire News Room· 2024-08-26 14:41
Core Insights - Altamira Therapeutics Ltd. has made significant advancements in immune checkpoint inhibitor therapy using Zbtb46 mRNA delivered via SemaPhore nanoparticles, showing promising results in animal tumor models with a significant tumor size reduction (p<0.0001) [1] - The Zbtb46 gene plays a crucial role in modifying the tumor microenvironment, enhancing the effectiveness of anti-PD1 treatments and leading to improved outcomes in cancer patients [2] - Altamira Medica's Bentrio nasal spray has been confirmed free of WADA prohibited substances, making it safe for athletes and addressing allergy management without doping risks [2] - Preclinical data indicates that SOD2 mRNA delivered via SemaPhore nanoparticles significantly reduces abdominal aortic aneurysm progression and improves survival rates (p<0.01) [3][4] - Altamira Therapeutics is expanding the distribution of Bentrio to Sweden and Denmark following its successful launch in Norway, aiming to establish a strong presence in the Scandinavian market [5] Company Developments - Altamira Therapeutics focuses on RNA-based treatments for non-liver targets using its OligoPhore and SemaPhore delivery platforms, with ongoing preclinical projects targeting KRAS-driven cancer and rheumatoid arthritis [6] - The company is divesting or out-licensing its legacy assets in allergology, viral infection, and inner ear therapeutics to streamline its focus on core projects [6] Research and Collaboration - The research on Zbtb46 mRNA was conducted by the Pathology & Immunology Department of Washington University School of Medicine, indicating strong academic collaboration [1] - The study on SOD2 mRNA was a joint effort between Washington University in St. Louis and the University of South Florida, highlighting the collaborative nature of Altamira's research initiatives [3][4]
Altamira Therapeutics Announces Extension of Bentrio Distribution Agreement with Pharma Nordic to Include Sweden and Denmark
GlobeNewswire News Room· 2024-08-23 13:01
Core Insights - Altamira Therapeutics has successfully launched Bentrio in Norway and has extended its exclusive distribution agreement with Pharma Nordic AS to include Sweden and Denmark, aiming to introduce the product in these markets next year [1][2] Company Overview - Altamira Therapeutics is focused on developing peptide-based nanoparticle technologies for RNA delivery, with two flagship siRNA programs in preclinical development targeting KRAS-driven cancer and rheumatoid arthritis [4] - The company holds a 49% stake in Altamira Medica AG, which commercializes Bentrio, an OTC nasal spray for allergic rhinitis [4] Product Details - Bentrio is a drug-free nasal spray designed to protect against airborne allergens and viruses, forming a protective gel layer in the nasal mucosa [3] - Clinical trials, including the NASAR study with 100 participants, demonstrated Bentrio's efficacy in reducing nasal symptoms and improving quality of life compared to saline [3] Market Expansion - The positive reception of Bentrio in Norway has prompted plans for its introduction in Sweden and Denmark, where there is a shared interest in innovative healthcare products [2][3]
Altamira Therapeutics Announces Confirmed Suitability of Bentrio for Athletes as Comprehensive Testing Shows Absence of Prohibited Substances
GlobeNewswire News Room· 2024-08-16 13:01
Core Insights - Altamira Medica Ltd. announced that its Bentrio® nasal spray has been independently tested and found free of over 230 prohibited substances listed by the World Anti-Doping Agency (WADA), confirming its suitability for athletes [1][3] - The nasal spray is designed to protect against airborne allergens and particles while complying with anti-doping regulations, addressing the challenges athletes face in managing allergic rhinitis [2][3] Company Overview - Altamira Therapeutics Ltd. is focused on developing peptide-based nanoparticle technologies for RNA delivery, with two flagship siRNA programs in preclinical development targeting KRAS-driven cancer and rheumatoid arthritis [5][6] - The company holds a 49% stake in Altamira Medica AG, which commercializes Bentrio®, an over-the-counter nasal spray for allergic rhinitis [6] Product Details - Bentrio® is a drug-free and preservative-free nasal spray that forms a protective gel layer on the nasal mucosa, preventing airborne particles from contacting cells and aiding in their discharge [4] - Clinical trials, including the NASAR study with 100 participants, demonstrated Bentrio's efficacy in reducing allergy symptoms and improving quality of life, with statistically significant results [4]
Altamira Therapeutics Announces Significant Enhancement of Immune Checkpoint Inhibition Therapy in Combination with Zbtb46 mRNA Delivered with SemaPhore Nanoparticles in Animal Tumor Models
GlobeNewswire News Room· 2024-08-12 13:02
Core Insights - Altamira Therapeutics has published significant findings regarding the Zbtb46 mRNA nanoparticles, demonstrating a substantial reduction in tumor growth and potential for long-term remission when combined with anti-PD1 therapies [1][2][3] Group 1: Research Findings - Treatment with ZbtbB46 mRNA nanoparticles resulted in a significant reduction in tumor growth (p<0.0001) [1] - The combination of Zbtb46 mRNA nanoparticles with anti-PD1 immune checkpoint inhibitors showed enhanced tumor control and long-term complete remission in many cases [1][3] - The study highlighted the role of the Zbtb46 gene in tumor angiogenesis and anti-tumor immunity, indicating that enforced expression of Zbtb46 can mitigate pro-tumor microenvironment features [2][3] Group 2: Mechanism and Implications - Zbtb46 is critical for maintaining a healthy tumor microenvironment, as its downregulation leads to dysfunctional vasculature and immunosuppressive conditions [2] - The research suggests that Zbtb46 mRNA nanoparticles can create favorable conditions for anti-PD1 treatments, potentially expanding the patient population that can benefit from these therapies [2][3] - The combination therapy not only improved treatment outcomes but also indicated the development of immunological memory, as mice did not develop new cancers after treatment [3] Group 3: Technology Overview - Altamira's SemaPhore platform is designed for effective mRNA delivery to non-hepatic tissues, utilizing a proprietary peptide for rapid self-assembly into nanoparticles [4] - The SemaPhore technology protects RNA from degradation and facilitates efficient cellular uptake, demonstrating positive outcomes in various disease models [4] Group 4: Company Background - Altamira Therapeutics is focused on developing peptide-based nanoparticle technologies for RNA delivery, with ongoing preclinical programs targeting KRAS-driven cancer and rheumatoid arthritis [5] - The company also holds a significant stake in Altamira Medica AG, which markets Bentrio®, an OTC nasal spray for allergic rhinitis [5]
Altamira Therapeutics Announces Publication of Preclinical Data Showing Successful Treatment of Abdominal Aortic Aneurysm with SOD2 mRNA Delivered by SemaPhore Nanoparticles
Newsfilter· 2024-07-19 13:01
Core Insights - The study demonstrates that Altamira's SemaPhore™ nanoparticles effectively deliver SOD2 mRNA to the aorta, resulting in significant reductions in aorta dilation, delayed rupture, and improved survival rates in an animal model of abdominal aortic aneurysm (AAA) [5][6]. Company Overview - Altamira Therapeutics is focused on developing RNA delivery technologies for targets beyond the liver, with a particular emphasis on peptide-based nanoparticle platforms like OligoPhore™ and SemaPhore™ [2][5]. - The company is advancing two flagship siRNA programs, AM-401 for KRAS-driven cancer and AM-411 for rheumatoid arthritis, both currently in preclinical development [2]. - Altamira holds a 49% stake in Altamira Medica AG, which markets Bentrio®, an OTC nasal spray for allergic rhinitis, and is exploring partnerships or divestments for its inner ear legacy assets [2][5]. Research Findings - The study, conducted by researchers from Washington University and the University of South Florida, indicates that systemic delivery of SOD2 mRNA via SemaPhore nanoparticles significantly mitigates AAA progression and enhances survival rates [5][6]. - The treatment approach targets oxidative stress, a key factor in AAA pathology, by boosting mitochondrial SOD2 expression, thereby reducing reactive oxygen species (ROS) levels [6]. Market Implications - The positive outcomes from the study suggest potential applications for SemaPhore nanoparticles in managing small AAAs and preventing ruptures, which could lead to new treatment options in the cardiovascular field [5][6].
Altamira Therapeutics Announces Publication of Preclinical Data Showing Successful Treatment of Abdominal Aortic Aneurysm with SOD2 mRNA Delivered by SemaPhore Nanoparticles
GlobeNewswire News Room· 2024-07-19 13:01
Core Insights - The study demonstrates that Altamira's SemaPhore™ nanoparticles effectively deliver SOD2 mRNA to the aorta, resulting in significant reductions in aorta dilation, delayed rupture, and improved survival rates in an established animal model of abdominal aortic aneurysm (AAA) [1][7][11] Company Overview - Altamira Therapeutics is focused on developing peptide-based nanoparticle technologies for efficient RNA delivery to extrahepatic tissues, with its SemaPhore™ platform being a key component [5][7] - The company has two flagship siRNA programs in preclinical development, targeting KRAS-driven cancer and rheumatoid arthritis, and is also exploring applications for mRNA delivery [5][7] Research Findings - The study conducted by researchers from Washington University and the University of South Florida showed that systemic delivery of SOD2 mRNA via SemaPhore nanoparticles significantly reduced oxidative stress and mitigated the expansion of small AAAs [1][11] - The treatment resulted in a statistically significant improvement in survival rates (p<0.01) compared to untreated controls, indicating the potential for clinical application in managing small AAAs and preventing ruptures [1][7][11] Clinical Implications - The findings suggest that targeting oxidative stress through SOD2 mRNA delivery could be a promising therapeutic strategy for various cardiovascular disorders, including AAA and atherosclerosis [1][11] - The safety profile of the nanoparticles was favorable, with no adverse effects on major organs or hematologic parameters observed [1][11]
Altamira Therapeutics Highlights Newly Published Review Article Supporting Use of Betahistine in Vertigo Management
GlobeNewswire News Room· 2024-06-20 13:01
Core Insights - The article discusses the treatment of residual dizziness following physical repositioning procedures for benign paroxysmal positional vertigo (BPPV), highlighting the role of betahistine and its intranasal formulation AM-125 developed by Altamira Therapeutics [7][9]. Group 1: BPPV and Its Impact - BPPV is the most common type of vertigo, accounting for 17% to 42% of all diagnosed cases, with healthcare costs in the U.S. approaching $2 billion annually [8]. - Approximately 31% to 61% of BPPV patients experience residual dizziness after treatment, which can significantly affect their quality of life [7][8]. - Almost 86% of BPPV patients report interruptions to daily activities and lost workdays due to their condition [8]. Group 2: Betahistine and Its Formulations - Betahistine is recognized as a standard treatment for dizziness and vertigo, marketed worldwide except in the U.S., but its oral formulation has limited clinical utility due to poor bioavailability [4][7]. - AM-125, an intranasal formulation of betahistine, has demonstrated 5 to 29 times higher bioavailability compared to the oral version, making it a promising treatment option for U.S. patients [5][9]. - The combination of physical repositioning procedures with betahistine treatment has shown a significantly greater reduction in dizziness handicap compared to the procedure alone, with a p-value of 0.001 [2][6]. Group 3: Altamira Therapeutics and Strategic Focus - Altamira Therapeutics is pivoting towards RNA delivery technology while developing AM-125 as part of its legacy assets [5][9]. - The company is exploring partnerships or divestments for AM-125 to enhance its market reach and availability in the U.S. [7][9]. - Altamira's current projects include two flagship siRNA programs for cancer and rheumatoid arthritis, both in preclinical development [5].
Altamira Therapeutics Highlights Newly Published Review Article Supporting Use of Betahistine in Vertigo Management
Newsfilter· 2024-06-20 13:01
Company Overview - Altamira Therapeutics is focused on developing and commercializing RNA delivery technology for targets beyond the liver, with a notable emphasis on peptide-based nanoparticle technologies [9] - The company is developing AM-125, an intranasal formulation of betahistine, to improve bioavailability and provide treatment options for patients in the US [5][15] - Altamira is also working on strategic partnerships or divestments of its legacy assets, including AM-125, as part of a pivot towards RNA delivery technology [5][7] Industry Context - Benign paroxysmal positional vertigo (BPPV) is the most common type of vertigo, accounting for 17% to 42% of all diagnosed cases, with healthcare costs in the US approaching $2 billion annually [12] - Residual dizziness occurs in 31% to 61% of BPPV patients, significantly affecting their quality of life and daily activities [11][12] - Betahistine is considered a standard treatment for dizziness and vertigo, with its oral formulation approved in approximately 115 countries, although it is not available in the US [5][14] Treatment Insights - The combination of physical repositioning procedures and betahistine treatment has shown a significantly greater reduction in dizziness handicap compared to the procedure alone, with a p-value of 0.001 [5][10] - AM-125 has demonstrated 5-to-29 times higher bioavailability than orally administered betahistine, which may enhance treatment efficacy for vestibular disorders [15] - The company aims to test AM-125 specifically for BPPV, as treatment for this condition is a primary indication for betahistine [7]