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Autonomix Medical, Inc. Announces Abstract Selected for Poster Presentation at the 2026 American Society of Clinical Oncology (ASCO) Gastrointestinal Cancers Symposium
Globenewswire· 2025-12-18 13:30
Company Overview - Autonomix Medical, Inc. is a medical device company focused on advancing innovative technologies for diagnosing and treating diseases involving the nervous system [3] - The company's first-in-class platform system technology includes a catheter-based microchip sensing array designed to detect and differentiate neural signals with greater sensitivity than existing technologies [3] - The technology aims to enable transvascular diagnosis and treatment of peripheral nervous system diseases throughout the body [3] Product Development - The initial focus of the technology is on pain treatment, specifically targeting pancreatic cancer, which is known for causing severe pain and lacks reliable treatment options [4] - The technology has the potential to address a wide range of indications, including cardiology, hypertension, and chronic pain management [4] - The technology is currently investigational and has not yet received marketing clearance in the United States [4] Upcoming Presentation - Autonomix announced that its abstract has been accepted for poster presentation at the 2026 ASCO Gastrointestinal Cancers Symposium [1] - The presentation will focus on a long-term analysis of pain mitigation in pancreatic adenocarcinoma through denervation via transvascular RF energy-based ablation [1] - The poster session is scheduled for January 9, 2026, with specific time slots for presentation [1]
Ventripoint Diagnostics Announces Collaboration with Summit Sciences
Thenewswire· 2025-12-18 13:10
Core Insights - Ventripoint Diagnostics Ltd. has engaged Dana Friesen and Summit Sciences to develop advanced financial and ROI models aimed at enhancing the economic evaluation of its VMS+ technology for cardiac diagnostics [1][2][3] Group 1: Strategic Partnership - The collaboration focuses on refining financial modeling frameworks that emphasize cost savings, operational efficiencies, and clinical outcomes associated with Ventripoint's AI-driven 3D heart modeling system [2] - This partnership aims to provide tailored insights for healthcare providers, demonstrating clear ROI through improved processes and resource allocation [2][3] Group 2: Leadership and Expertise - Hugh MacNaught, President & CEO of Ventripoint, expressed enthusiasm about the partnership, highlighting the combined expertise of Dana Friesen in healthcare transformation and Summit Sciences' data-driven consulting [3] - Dana Friesen, CEO of Summit Sciences, noted the importance of real-world data in accelerating the commercialization of VMS+ and expanding access to advanced cardiac imaging [3] Group 3: Technology Overview - Ventripoint's VMS+ platform utilizes AI to create accurate 3D models of the heart from standard 2D ultrasound images, providing a faster and more affordable alternative to traditional MRI scans [4] - The VMS products are based on proprietary Knowledge Based Reconstruction technology, offering accurate volumetric cardiac measurements equivalent to MRI [5] Group 4: Summit Sciences Background - Summit Sciences has a two-decade history of working with clinical agencies, delivering billions in lifetime partner savings through critical data for informed decision-making in technology adoption [6] - The firm employs advanced research methodologies to provide actionable insights that enhance patient care while optimizing resource utilization [6][7]
Johnson & Johnson Receives FDA Approval for TRUFILL n‑BCA Liquid Embolic System for the Treatment of Symptomatic Chronic Subdural Hematoma
Prnewswire· 2025-12-18 13:00
Core Insights - Johnson & Johnson MedTech has received FDA approval for an expanded indication of the TRUFILL n-BCA Liquid Embolic System for the embolization of the middle meningeal artery (MMA) to treat symptomatic subacute and chronic subdural hematoma (cSDH) as an adjunct to surgery [2][3] Group 1: Product and Approval Details - TRUFILL n-BCA has been a trusted solution in neurovascular embolization for over 25 years, originally approved in 2000 for treating arteriovenous malformations (AVMs) [4] - The approval is based on findings from the MEMBRANE randomized controlled trial, which showed TRUFILL n-BCA to be superior in effectiveness compared to the standard of care for embolization in MMA for treating symptomatic cSDH [3][4] - cSDH is often caused by minor head trauma, particularly in older adults and those on anticoagulation therapy, with recurrence rates estimated between 10% to 20% [2] Group 2: Clinical Significance - The MEMBRANE study demonstrated a positive treatment effect in favor of TRUFILL n-BCA, reinforcing its potential to improve outcomes for patients with cSDH [4][9] - The embolization of the MMA offers a minimally invasive endovascular approach, targeting smaller brain vessels that contribute to hematoma persistence and regrowth [2][3] Group 3: Industry Context - Johnson & Johnson MedTech is committed to addressing complex health challenges, including those related to neurovascular care, and aims to provide innovative technologies that improve patient outcomes [5][6] - The company is recognized as a global leader in various medical fields, including cardiovascular solutions, and is focused on tackling significant health issues such as heart failure and stroke [5][6]
Catheter Precision (VTAK) Announces Expansion of LockeT into an Eighth European Country Since Receipt of CE Mark
Globenewswire· 2025-12-18 13:00
Company secures first purchase order and multi-year commitment at Ireland’s largest electrophysiology centerFort Mill, SC, Dec. 18, 2025 (GLOBE NEWSWIRE) -- Catheter Precision, Inc. (VTAK - NYSE/American), a leader in advanced electrophysiology solutions, today announced the successful implementation of LockeT and the first LockeT purchase order at Mater Private Hospital, located in Dublin, Ireland. This marks a significant milestone in the company’s global expansion strategy and reinforces its commitment ...
Better Buy in 2026: Novo Nordisk or Intuitive Surgical?
Yahoo Finance· 2025-12-18 12:05
Group 1 - Novo Nordisk and Intuitive Surgical are both leaders in the healthcare sector but operate in different areas, with Novo Nordisk focusing on pharmaceutical drugs and Intuitive Surgical on robotic-assisted surgery devices [1] - Both companies have faced challenges this year, resulting in below-average stock-market performances, but there is potential for recovery in the coming years [2] Group 2 - Novo Nordisk's financial results have not met investor expectations, with a decline in top-line growth and a lowered outlook due to losing ground in the GLP-1 market, which is crucial for its revenue [4] - The company is expected to launch new products, including CagriSema, which, despite not meeting the target of 25% mean weight loss, achieved a competitive 22.7%, potentially aiding its position in the crowded GLP-1 market [5] - Recent and pending label expansions for semaglutide, including new approvals for reducing cardiovascular event risks and treating metabolic dysfunction-associated steatohepatitis, could enhance Novo Nordisk's sales growth [6] - Novo Nordisk's sales increased by 12% year over year to 229.9 billion Danish kroner ($36.2 billion) in the first nine months of the year, while net profit rose by 4% to 75.5 billion DKK ($11.9 billion) [7] Group 3 - Intuitive Surgical is expected to maintain its leadership in the robotic-assisted surgery niche despite facing increased competition [8] - Both Novo Nordisk and Intuitive Surgical have the potential to be long-term winners, with investment choices depending on individual risk tolerance [8]
Edwards Lifesciences to Present at the 44th Annual J.P. Morgan Healthcare Conference
Businesswire· 2025-12-18 12:05
IRVINE, Calif.--(BUSINESS WIRE)--Edwards Lifesciences Corporation (NYSE: EW) today announced it will participate in the J.P. Morgan Healthcare Conference on Monday, Jan. 12, 2026. Bernard Zovighian, chief executive officer, is scheduled to present at 11:15 a.m. PT. Scott Ullem, chief financial officer, will also participate in the conference. A live webcast of the presentation will be available on the Edwards Lifesciences investor relations website at http://ir.edwards.com/, with an archived version access ...
4只新股同日上市 共募资约70亿美元
Sou Hu Cai Jing· 2025-12-18 06:23
Group 1: Medline (MDLN) - Medline opened at $35 per share, a 20.69% increase from the offering price, and closed at $41, marking a 41.38% rise with a total market capitalization of $75.563 billion [2][4] - The company issued 216 million shares at $29 each, raising $6.265 billion, with plans to use the funds for debt repayment and general corporate purposes [4] - Medline is a leading global manufacturer and distributor of medical supplies, producing hundreds of thousands of consumable medical products including surgical gloves, gowns, dressings, and surgical packs [4] Group 2: Andersen (ANDG) - Andersen opened at $21 per share, a 31.25% increase from the offering price, and closed at $23.5, reflecting a 46.88% rise with a total market capitalization of $2.569 billion [5][7] - The company issued 11 million shares at $16 each, raising $176 million, with plans to invest in technology, infrastructure, training, and potential strategic acquisitions [7] - Andersen provides independent tax, valuation, and financial consulting services to individuals, family offices, businesses, and institutional clients, having served 11,900 clients as of September 30, 2025 [7] Group 3: SPACs - Churchill Capital XI (CCXIU) raised $360 million, while Iron Horse Acquisition II (IRHOU) raised $200 million [8] - Churchill Capital XI, initiated by Michael Klein, aims to target companies with stable revenues and strong management teams [8] - Iron Horse Acquisition II, led by Jose Bengochea, focuses on the media and entertainment industry, particularly in music, animation, and artificial intelligence [8]
Activist Irenic Pushing Medical-Device Maker Integer to Pursue Sale
WSJ· 2025-12-17 22:00
Group 1 - A hedge fund with over a 3% stake in Integer has sent a letter to the company's board outlining its requests [1]
Aptar's Bidose Nasal System Delivers CARDAMYST™ (etripamil), the First and Only Self-Administered FDA-Approved Nasal Spray for Paroxysmal Supraventricular Tachycardia (PSVT)
Businesswire· 2025-12-17 22:00
Core Viewpoint - Aptar Group, Inc. has announced that its Bidose Liquid Nasal Spray System will be used for the newly approved CARDAMYST Nasal Spray, which is intended for treating acute symptomatic episodes of paroxysmal supraventricular tachycardia (PSVT) [1] Company Summary - Aptar Group, Inc. is recognized as a global leader in drug and consumer product dosing, dispensing, and protection technologies [1] - The Bidose Liquid Nasal Spray System is a key product in Aptar's portfolio, showcasing its capabilities in drug delivery systems [1] Industry Summary - The approval of CARDAMYST by the U.S. Food and Drug Administration (FDA) highlights advancements in treatment options for PSVT, indicating a growing market for innovative drug delivery systems [1]
Defender Capital Reiterates Intention to Vote AGAINST STAAR Surgical's Proposed Sale to Alcon Inc.
Prnewswire· 2025-12-17 21:53
Core Viewpoint - Defender Capital expresses disappointment in STAAR Surgical Company's Board of Directors' continued pursuit of a sale to Alcon Inc., believing it is not in the best interests of STAAR shareholders and does not reflect adequate value for the Company [1]. Group 1: Timing and Valuation Concerns - The proposed sale to Alcon is viewed as occurring at the wrong time and price for STAAR shareholders, especially given STAAR's recent global growth and the stabilization of its business [2]. - The timing of the deal is criticized as opportunistic for Alcon, particularly as STAAR's business shows potential upside following recent earnings reports [2]. Group 2: Flawed Process - The process leading to the deal has been deemed flawed, with recommendations from Glass Lewis and ISS advising shareholders to vote against it [3]. - Concerns were raised about event-driven hedge funds purchasing STAAR shares without understanding the opposition from major shareholders like Broadwood Partners, leading to a decline in stock price [3]. Group 3: Vote Delay and Due Diligence - STAAR's Board delayed the vote until December 19 and reopened the bidding process, raising questions about the adequacy of the time allowed for potential acquirers to conduct due diligence, especially given the significance of the Chinese market to STAAR's business [4]. - No new bids emerged following the delay, indicating a lack of interest from other potential buyers [4]. Group 4: Continued Opposition - Defender Capital intends to vote against the transaction, citing a lack of compelling reasons to sell STAAR at this time and expressing disappointment in the Board's actions [5].