Home Blog Page 1107

ZEISS launches Collaborative Care application to strengthen continuity of care; new solution offers on-premises and cloud-based options

Built on the ZEISS Health Data Platform, ZEISS Collaborative Care offers eye care professionals a flexible way to collaborate – whether as a standalone cloud application or as an integrated extension of ZEISS FORUM – enabling secure data sharing, structured referrals, and real-time clinical coordination to strengthen continuity of care across the ophthalmic workflow.

JENA, Germany, Feb. 23, 2026 /PRNewswire/ — ZEISS Medical Technology, one of the world’s leading medical technology companies, today launched its ZEISS Collaborative Care browser-based software application enabling eye care professionals to seamlessly work together securely sharing data, referring patients, and strengthening their professional networks. The new solution addresses longstanding challenges in ophthalmic care, particularly fragmented data sharing, and inefficient referral processes. By enabling real-time communication, structured referrals, and shared clinical insights, ZEISS Collaborative Care empowers providers to make fast and confident clinical decisions.

ZEISS Collaborative Care
ZEISS Collaborative Care

ZEISS Collaborative Care will be demonstrated for the first time at the 100% Optical 2026 congress in London from Feb. 28 to March 2, and then again at the Vision Expo event in Orlando, FL, from March 11 to 14.

“At ZEISS, we’ve focused the strengths of our digital expertise to address some of the persistent challenges in a patient’s healthcare journey. Working closely with our customers, we’ve laid the foundation to transform continuity of care today, supported by data-driven, digital care models that can follow patients throughout their ophthalmic care pathway. ZEISS Collaborative Care is an important step forward in our vision, bringing care teams closer together for more efficient patient care,” says Magnus Reibenspiess, Chief Commercial Officer and Head of Strategic Business Unit Ophthalmology at ZEISS Medical Technology.  

A new standard for connected care

ZEISS Collaborative Care is delivered as an application of the ZEISS Healthcare Data Platform (HDP), which provides the secure cloud foundation behind our digital solutions. As an HDP-powered application, it offers flexible deployment for practitioners to support a wide range of clinical environments. Practices may use it as a standalone cloud solution or as a connected extension of ZEISS FORUM allowing diagnostic data, images, and insights to flow seamlessly from on-premises systems into secure, browser-based collaboration spaces. This flexibility ensures providers – regardless of their current digital infrastructure – can participate in efficient, data-driven care pathways.

ZEISS Collaborative Care offers an intuitive set of real-time collaboration tools, ensuring clinical data moves with the patient, supporting better decisions and more coordinated care. It integrates smoothly into existing ZEISS solutions and adheres to industry standard security requirements, enabling eye care professionals to collaborate with confidence.

SHARE – exchange insights and data to enhance decision-making

  • Securely exchanging images, reports and patient data to obtain second opinions and foster more confident clinical decision-making.
  • Consult with peers on challenging cases to validate assessments and determine the best care pathway for patients.
  • Communicate in real-time via chat and stay updated with email notifications.

REFER – streamline referral workflows

  • Send, track and prioritize referrals through a user-friendly, secure browser-based application, ensuring the right data gets to the right provider at the right time.
  • Facilitate seamless patient care updates between referring and receiving practitioners, optimizing the patient journey from consultation to specialist care.
  • Easily receive and download patient data into the eye care professional’s system for comprehensive analysis and documentation.

NETWORK – strengthen professional networks to improve continuity of care

  • Build stronger professional connections and trust between optometrists and ophthalmologists, and foster an open network dedicated to better patient care.
  • Exchange clinical knowledge and access peer support anytime, anywhere to enhance the eye care professional’s practice.
  • Collaborate within a professional network via a browser, independent of any one data management system.

For more information about ZEISS Collaborative Care visit here.

Not all products, services or offers are approved or offered in every market and approved labeling and instructions may vary from one country to another. For country-specific product information, see the appropriate country website. Product specifications are subject to change in design and scope of delivery as a result of ongoing technical development. The statements of the healthcare professionals reflect only their personal opinions and experiences and do not necessarily reflect the opinion of any institution that they are affiliated with. The healthcare professionals alone are responsible for the content of their experience reported and any potential resulting infringements. Carl Zeiss Meditec AG and its affiliates to not have clinical evidence supporting the opinions and statements of the health care professionals nor accept any responsibility or liability of the healthcare professionals’ content. The healthcare professionals have a contractual or other financial relationship with Carl Zeiss Meditec AG and its affiliates and have received financial support.

Contact for investors:
Sebastian Frericks
Director Investor Relations
Carl Zeiss Meditec AG
Phone: +49 3641 220 116
Mail: investors.med@zeiss.com

Contact for the press:
Frank Smith
Head of Global Communications
Ophthalmology, Carl Zeiss Meditec Inc.
Phone: +49 3641 220 331
Mail: press.med@zeiss.com

Company Profile

Carl Zeiss Meditec AG (ISIN: DE0005313704), which is listed on the MDAX and TecDAX of the German stock exchange, is one of the world’s leading medical technology companies. The Company supplies innovative technologies and application-oriented solutions designed to help doctors improve the quality of life of their patients. The Company offers complete solutions, including implants and consumables, to diagnose and treat eye diseases. The Company creates innovative visualization solutions in the field of microsurgery. With 5,784 employees worldwide, the Group generated revenue of €2,228m in fiscal year 2024/25 (to 30 September).

The Group’s head office is located in Jena, Germany, and it has subsidiaries in Germany and abroad; more than 50 percent of its employees are based in the USA, Japan, Spain and France. The Center for Application and Research (CARIn) in Bangalore, India and the Carl Zeiss Innovations Center for Research and Development in Shanghai, China, strengthen the Company’s presence in these rapidly developing economies. Around 39 percent of Carl Zeiss Meditec AG’s shares are in free float. Approx. 59 percent are held by Carl Zeiss AG, one of the world’s leading groups in the optical and optoelectronic industries.

For further information visit: www.zeiss.com/med

 

“Would You Clone Yourself for a Cure?” Clonell Unveils White Paper on Fundamental Cures for 34 Incurable Diseases Using ‘Human Cloning’ Technology

Harnessing the vitality of a clone while neutralizing ethical controversies through a breakthrough ‘Therapeutic Cloning’ protocol—ushering in a new era of regenerative medicine to conquer cancer, Alzheimer’s, and aging.

YONGIN, South Korea, Feb. 23, 2026 /PRNewswire/ — Human cloning has long been a subject of dystopian science fiction and a stringent ethical taboo. However, Clonell Therapeutics, Inc., a cutting-edge biotechnology company, is actively shaking the landscape of regenerative medicine by bringing this powerful, historically controversial technology into the clinical setting in an entirely ethical and legal form.

Pioneering the clinical application of human cloning technology, Clonell today officially released a comprehensive therapeutic white paper on its global website (https://www.clonell.com). The white paper details ultimate treatment protocols for 34 conditions currently classified as incurable diseases. The medical community’s attention is highly focused, as the target diseases encompass not only Alzheimer’s disease, Parkinson’s disease, and myocardial infarction, but also cancer and even aging itself.

How can a single technology target such a broad spectrum of diseases simultaneously? According to Clonell’s white paper, the answer lies in precisely targeting ‘Cellular Senescence’—the common underlying culprit behind modern diseases. Moving beyond the limitations of conventional medicine, which has primarily focused on symptom management and suppressing disease progression, Clonell’s approach envisions completely replacing the old, diseased cells that comprise failing organs with young, healthy cells from the patients themselves.

The crucial challenge has always been how to generate these miraculous cells. Here, Clonell has played its most unconventional and transformative card: ‘Human Cloning.’ Cells generated through human cloning technology are a 100% genetic match to the patient, resulting in zero immune rejection. Simultaneously, their biological age is reset to ‘zero,’ granting them the explosive regenerative power observed only in the earliest stages of life. A therapeutic agent satisfying both of these critical conditions has never existed in the history of regenerative medicine.

Dr. Hyo-Sang Lee, currently the Chief Scientific Officer at Clonell and a key protagonist of the Oregon Health & Science University (OHSU) research team that successfully established the world’s first SCNT-hESCs (Somatic Cell Nuclear Transfer-derived Human Embryonic Stem Cells, the original paper) from a cloned human embryo in 2013, stated:

“To fundamentally cure diseased organs, we require cells that our body’s immune system will not reject, while also possessing a youthful vigor strong enough to rebuild the damaged organ. However, apart from human cloning technology, no existing treatment has been able to satisfy both conditions simultaneously. Until now, medicine has always been forced to choose one or the other. The reason degenerative diseases, including aging, have remained unconquered is simply that the cells capable of solving this core dilemma did not exist.”

Does this mean Clonell is creating human clones? Not at all. Clonell’s cloned cells begin with SCNT, the core technology of human cloning, where a patient’s somatic cell is fused with an enucleated oocyte to create a cloned embryo. However, instead of transferring this cloned embryo into a surrogate to create a fully formed human clone—a method known as ‘Reproductive Cloning’—Clonell utilizes a ‘Therapeutic Cloning’ approach. The company extracts cells from the blastocyst after culturing it in a laboratory for seven days. Ultimately, this is a highly intelligent strategy: safely capturing the perfect biocompatibility and biological age-zero vitality of a clone, without ever creating a living, breathing human organism.

Dr. Lee further emphasized, “We have finally found the master key to harness the explosive vitality equivalent to that of a human clone for patient treatment, while strictly adhering to all bioethical standards. Human cloning technology is no longer science fiction or an ethical taboo. It is a highly effective, practical medical tool for fighting incurable diseases and represents the most perfect biological cure humanity has ever dreamed of.”

Detailed disease-specific treatment protocols and mechanisms for the 34 incurable diseases proposed by Clonell are now available to the public and scientific community on the official website (https://www.clonell.com).

About Clonell Therapeutics, Inc.

Clonell™ is a state-of-the-art biotechnology company dedicated to developing fundamental cures for intractable and incurable diseases through human cloning technology (Therapeutic Cloning). Built upon unrivaled technological expertise, the company boasts an extensive therapeutic pipeline addressing neurodegenerative diseases, cardiovascular diseases, and aging-related conditions. With ‘patient-centric innovation’ as its highest core value, Clonell is ushering in a new era of personalized regenerative medicine by introducing an unprecedented paradigm: the ‘Patient-Initiated Clinical Trial™,’ empowering patients to proactively lead the clinical journey for their own cures.

Media Contact Clonell Therapeutics, Inc. Public Relations Email: media@clonell.com

LOCKSLEY RESOURCES COMMENCES DRILLING AT ITS HIGH-GRADE DESERT ANTIMONY MINE LOCATED WITHIN THE COMPANY’S MOJAVE PROJECT IN CALIFORNIA

SAN BERNARDINO, Calif., Feb. 23, 2026 /PRNewswire/ — Locksley Resources Limited (ASX: LKY, OTCQX: LKYRF and LKYLY-ADR) announced the company has commenced diamond drilling at the high-grade Desert Antimony Mine (DAM), located within the company’s Mojave Project in California.

The drilling follows successful completion of site establishment activities including necessary earthworks and construction of drill pads. During these site preparations, the company also conducted detailed surface explore mapping that provided critical geological data and confirmed the orientation and continuity of the primary stibnite veins at surface. More information is available here: https://cdn-api.markitdigital.com/apiman-gateway/ASX/asx-research/1.0/file/2924-03059509-6A1313161&v=undefined.

Kerrie Matthews, Managing Director and CEO of Locksley said, “The start of drilling at DAM is a key milestone for us. We have strong momentum as we move decisively to unlock a potential asset that can play an important role in reshaping the future of critical minerals supply.” She noted that the commencement of drilling reflects a strong technical foundation and focus on high-confidence target areas.

“In parallel to our drilling program, we are also carrying out our downstream metallurgical testwork, with representative materials to be supplied to Rice University and the Department of Energy to support evaluation of pilot-scale processing and strengthen strategic positioning within critical mineral supply chains,” Matthews said.

Antimony is designated as a critical mineral by the U.S. government, with limited current domestic production. The Desert Antimony Mine represents a rare opportunity to establish a primary, high-grade antimony source within the U.S. aligned with national security, defense and advanced materials supply chains.

Locksley Resources (https://www.locksleyresources.com.au) is focused on critical minerals in the U.S. The company is actively advancing the Mojave Project in California, targeting rare earth elements (REEs) and antimony. Locksley is executing a mine-to-market strategy for antimony, aimed at reestablishing domestic supply chains for critical materials, underpinned by strategic downstream technology partnerships with leading U.S. research institutions and industry partners. This targeted approach, combined with resource development with innovative processing and separation technologies, positions Locksley to play a role in advancing U.S. critical materials independence.

Contact: Beverly Jedynak, beverly.jedynak@viriathus.com, 312-943-1123; 773-350-5793 (cell)

MDJM Advances Animation Art and Cultural Platform Development Strategy

LONDON, Feb. 23, 2026 /PRNewswire/ — MDJM Ltd. (the “Company”) today announced that it is advancing an animation art and cultural platform-oriented development strategy centered on Fernie Castle in Scotland, aligned with long-term growth objectives across the UK, European, and broader international markets.

The strategy focuses on three core pillars: cultural intellectual property (IP) development, physical cultural space construction, and digital extension capabilities. The Company intends to build a sustainable cultural asset framework designed to support future international expansion.

Cultural IP and International Collaboration

Through its subsidiary, MD Local Global Ltd., the Company continues to develop original animation content and international creative collaborations. The Company is gradually strengthening cross-border creator networks to support cultural engagement within the UK and European markets, while creating opportunities for broader international outreach over time.

Fernie Castle Animation Art Gallery Development

Development of the Fernie Castle Animation Art Gallery is progressing in accordance with established planning objectives. The project is expected to include permanent and temporary exhibitions, cultural programming, and educational initiatives designed to create a distinctive cultural experience environment. The Company plans to explore international cultural exchange opportunities at appropriate stages of development.

Digital Support Capabilities

The Company plans to introduce commercially available digital tools in phases to support exhibition content dissemination, multilingual cultural interpretation, and online presentation capabilities. These initiatives are intended to extend physical cultural experiences into digital environments and enhance cross-regional accessibility.

Platform-Oriented Development Direction

The Company intends to develop a platform-oriented operational framework centered on cultural IP, supported by physical cultural assets and digital capabilities. This approach is designed to enhance business coordination and long-term international development potential.

The Company believes that this strategic direction may strengthen its competitive positioning within the UK and European cultural markets and support future expansion toward broader international markets.

Investor Contact

Sherry Zheng
WAVECREST GROUP INC.
Phone: +1 718-213-7386
Email: sherry@wavecrestipo.com 

Bitmine Immersion Technologies (BMNR) Announces ETH Holdings Reach 4.423 Million Tokens, and Total Crypto and Total Cash Holdings of $9.6 Billion

Bitmine has 3,040,483 staked ETH, representing $6.0 billion at $1,958 per ETH; MAVAN staking solution on track to launch Q1 2026

Bitmine now owns 3.66% of the ETH token supply, over 73% of the way to the ‘Alchemy of 5%’ in just 7 months

Bitmine recently closed on initial $200 million investment into Beast Industries

Bitmine Crypto + Total Cash Holdings + “Moonshots” total $9.6 billion, including 4.423 million ETH tokens, total cash of $691 million, and other crypto holdings

Bitmine leads crypto treasury peers by both the velocity of raising crypto NAV per share and by the high trading liquidity of BMNR stock

Bitmine is the 165th most traded stock in the US, trading $0.7 billion per day (5-day avg)

Bitmine remains supported by a premier group of institutional investors including ARK’s Cathie Wood, MOZAYYX, Founders Fund, Bill Miller III, Pantera, Kraken, DCG, Galaxy Digital and personal investor Thomas “Tom” Lee to support Bitmine’s goal of acquiring 5% of ETH

LAS VEGAS, Feb. 23, 2026 /PRNewswire/ — (NYSE AMERICAN: BMNR) Bitmine Immersion Technologies, Inc. (“Bitmine” or the “Company”) a Bitcoin and Ethereum Network company with a focus on the accumulation of crypto for long term investment, today announced Bitmine crypto + total cash + “moonshots” holdings totaling $9.6 billion.

Bitmine weekly update
Bitmine weekly update

As of February 22th, 2026 at 6:00pm ET, the Company’s crypto holdings are comprised of 4,422,659 ETH at $1,958 per ETH (NASDAQ: COIN), 193 Bitcoin (BTC), $200 million stake in Beast Industries, $17 million stake in Eightco Holdings (NASDAQ: ORBS) (“moonshots”) and total cash of $691 million. Bitmine’s ETH holdings are 3.66% of the ETH supply (of 120.7 million ETH).

“In the midst of this ‘mini crypto winter,’ our focus continues to be on methodically executing our treasury strategy and steadily acquiring ETH and in turn, optimizing the yield on our ETH holdings,” said Thomas “Tom” Lee, Chairman of Bitmine.

“We discussed this operational strategy in our latest Chairman’s message (the link to his message is here). While crypto prices are attempting to find their respective lows, the three fundamental drivers for Ethereum continue to gain traction: (i) Wall Street and their efforts at tokenization; (ii) AI and agentic-AI using smart blockchains for both execution and for collecting payments and (iii) the emerging creator economy and their desire to use blockchains for verification,” continued Lee.

“In the past week, we acquired 51,162 ETH,” continued Lee. “Bitmine has been steadily buying Ethereum, as we view this pullback as attractive, given the strengthening fundamentals. In our view, the price of ETH is not reflective of the high utility of ETH and its role as the future of finance.”

As of February 22, 2026, Bitmine total staked ETH stands at 3,040,483 ($6.0 billion at $1,958 per ETH). “Bitmine has staked more ETH than other entities in the world. At scale (when Bitmine’s ETH is fully staked by MAVAN and its staking partners), the ETH staking rewards is $249 million annually (using 2.89% 7-day BMNR yield),” stated Lee.

“Annualized staking revenues are now $171 million. And this 3.0 million ETH is about 69% of the 4.4 million ETH held by Bitmine. The CESR (Composite Ethereum Staking Rate, administered by Quatrefoil) is 2.81%, while Bitmine’s own staking operations generated a 7-day yield of 2.89% (annualized). We continue to make progress on our staking solution known as The Made in America VAlidator Network (MAVAN). This will be the ‘best-in-class’ solution offering secure staking infrastructure and will be deployed in early calendar 2026. Bitmine is currently working with 3 staking providers as the Company moves towards unveiling MAVAN in 2026,” continued Lee.

Bitmine crypto holding reigns as the #1 Ethereum treasury and #2 global treasury, behind Strategy Inc. (NASDAQ: MSTR), which owns 717,131 BTC valued at $49 billion. Bitmine remains the largest ETH treasury in the world. 

Bitmine is one of the most widely traded stocks in the US. According to data from Fundstrat, the stock has traded average daily dollar volume of $0.7 billion (5-day average, as of February 20, 2026), ranking #165 in the US, behind Carnival Corp (rank #164) and ahead of Northrup Grumman (rank #166) among 5,704 US-listed stocks (statista.com and Fundstrat research).

The GENIUS Act and Securities and Exchange Commission’s (“the SEC”) Project Crypto are as transformational to financial services in 2025 as US action on August 15, 1971 ending Bretton Woods and the USD on the gold standard 54 years ago. This 1971 event was the catalyst for the modernization of Wall Street, creating the iconic Wall Street titans and financial and payment rails of today. These proved to be better investments than gold.

The Chairman’s message can be found here:
https://www.Bitminetech.io/chairmans-message

The Fiscal Full Year 2025 Earnings presentation and corporate presentation can be found here:
https://Bitminetech.io/investor-relations/

To stay informed, please sign up at: https://Bitminetech.io/contact-us/

About Bitmine
Bitmine (NYSE AMERICAN: BMNR) is the leading Ethereum Treasury company in the world, implementing an innovative digital asset strategy for institutional investors and public market participants. Guided by its philosophy of “the alchemy of 5%,” the Company is committed to ETH as its primary treasury reserve asset, leveraging native protocol-level activities including staking and decentralized finance mechanisms. The Company will launch MAVAN (Made-in America VAlidator Network), a dedicated staking infrastructure for Bitmine assets, in Q1 of 2026.

For additional details, follow on X:
https://x.com/bitmnr
https://x.com/fundstrat
https://x.com/bmnrintern

Forward Looking Statements
This press release contains statements that constitute “forward-looking statements.” The statements in this press release that are not purely historical are forward-looking statements which involve risks and uncertainties. This document specifically contains forward-looking statements regarding progress and achievement of the Company’s goals regarding ETH acquisition and staking, the long-term value of Ethereum, continued growth and advancement of the Company’s Ethereum treasury strategy and the applicable benefits to the Company. In evaluating these forward-looking statements, you should consider various factors, including Bitmine’s ability to keep pace with new technology and changing market needs; Bitmine’s ability to finance its current business, Ethereum treasury operations and proposed future business; the competitive environment of Bitmine’s business; and the future value of Bitcoin and Ethereum. Actual future performance outcomes and results may differ materially from those expressed in forward-looking statements. Forward-looking statements are subject to numerous conditions, many of which are beyond Bitmine’s control, including those set forth in the Risk Factors section of Bitmine’s Form 10-K filed with the SEC on November 21, 2025, as well as all other SEC filings, as amended or updated from time to time. Copies of Bitmine’s filings with the SEC are available on the SEC’s website at www.sec.gov. Bitmine undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.

STAKING: BMNR now staking over 3 million ETH
STAKING: BMNR now staking over 3 million ETH

 

ALCHEMY of 5%: BMNR ranked #165 by avg daily $ volume
ALCHEMY of 5%: BMNR ranked #165 by avg daily $ volume

 

 

TGE’s Film “Scare Out” Exceeds US$120 Million at the Box Office in just 7 Days

PARIS, NEW YORK and LONDON, Feb. 23, 2026 /PRNewswire/ — AMTD Group Inc. (“AMTD Group”), AMTD IDEA Group (NYSE: AMTD; SGX: HKB), AMTD Digital Inc. (NYSE: HKD) and The Generation Essentials Group (“TGE”, NYSE: TGE; LSE: TGE), a subsidiary of AMTD Digital Inc., jointly announce that “Scare Out” (the “Movie”), the first ever national‑security film co‑produced by TGE, captured a significant share of the box office during the Chinese New Year window. Featuring an all‑star cast including Jackson Yee, Yilong Zhu, Jia Song, Jiayin Lei, Mi Yang, Yi Zhang, Cecilia Liu, and Yaowen Liu, the Movie achieved box office inflows of over US$120 million within just its first seven days of release.

The Movie has also generated substantial traction on social media. Across major platforms, promotional content related to the Movie has attracted approximately 10.35 billion views, with daily increases of over 550 million views. On Douyin alone, the Movie’s hashtag has reached 5.32 billion views.

“Scare Out” represents a major success for TGE’s movie segment. Looking ahead to the second half of 2026 and into 2027, TGE‑produced films such as “Raging Havoc” and “Dog Day Evening” are scheduled for release. Both projects feature strong casts: “Raging Havoc” stars Andy Lau, Nicholas Tse, and Ci Sha, while “Dog Day Evening” features Michael Ning, Fish Liew, and Rachel Leung. TGE serves as a lead production company on both titles, with Dr. Calvin Choi, founder of AMTD IDEA, AMTD Digital, and TGE, acting as a Producer.

These upcoming releases are expected to further strengthen TGE’s movie portfolio and provide a solid foundation for future growth on a global basis.

TGE’s movie segment also continues to benefit from cross-segment synergies within the group. L’OFFICIEL, under TGE, has become a strategic media partner of the 44th Hong Kong Film Awards, and, with the continuous growth and strong developments of the L’OFFICIEL Movies business segment, is emerging as an important player in Hong Kong’s film media landscape. Internationally, L’OFFICIEL has conducted on-site coverage and interviews at major awards events such as the Golden Globe Awards and the British Academy Film Awards, and is expected to extend our presence at the Oscars this year. TGE will continue to strengthen and expand its global media outreaches and influential power, as a core part of its global media and entertainment IP businesses.

About AMTD Group

AMTD Group is a conglomerate with a core business portfolio spanning across media and entertainment, education and training, and premium assets and hospitality sectors.

About AMTD IDEA Group

AMTD IDEA Group (NYSE: AMTD; SGX: HKB) represents a diversified institution and digital solutions group connecting companies and investors with global markets. Its comprehensive one-stop business services plus digital solutions platform addresses different clients’ diverse and inter-connected business needs and digital requirements across all phases of their life cycles. AMTD IDEA Group is uniquely positioned as an active super connector between clients, business partners, investee companies, and investors, connecting the East and the West. For more information, please visit www.amtdinc.com or follow us on X (formerly known as “Twitter”) at @AMTDGroup.

About AMTD Digital Inc.

AMTD Digital Inc. (NYSE: HKD) is a comprehensive digital solutions platform headquartered in France. Its one-stop digital solutions platform operates key business lines including digital media, content and marketing services, investments as well as hospitality and VIP services. For AMTD Digital’s announcements, please visit https://ir.amtdigital.net/investor-news.

About The Generation Essentials Group

The Generation Essentials Group (NYSE: TGE; LSE: TGE), jointly established by AMTD Group, AMTD IDEA Group (NYSE: AMTD; SGX: HKB) and AMTD Digital Inc. (NYSE: HKD), is headquartered in France and focuses on global strategies and developments in multi-media, entertainment, and cultural affairs worldwide as well as hospitality and VIP services. TGE comprises L’Officiel, The Art Newspaper, movie and entertainment projects. Collectively, TGE is a diversified portfolio of media and entertainment businesses, and a global portfolio of premium properties. Also, TGE is a special purpose acquisition company (SPAC) sponsor manager, with its first SPAC successfully raised and priced on December 18, 2025.

Safe Harbor Statement

This press release contains statements that may constitute “forward-looking” statements pursuant to the “safe harbor”provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by terminology such as “will,” “expects,””anticipates,” “aims,” “future,” “intends,” “plans,” “believes,””estimates,” “likely to,” and similar statements. Statements that are not historical facts, including statements about the beliefs, plans, and expectations of AMTD IDEA Group, AMTD Digital and/or The Generation Essentials Group, are forward-looking statements. Forward-looking statements involve inherent risks and uncertainties. Further information regarding these and other risks is included in the filings of AMTD IDEA Group, AMTD Digital and The Generation Essentials Group with the SEC. All information provided in this press release is as of the date of this press release, and none of AMTD IDEA Group, AMTD Digital and The Generation Essentials Group undertakes any obligation to update any forward-looking statement, except as required under applicable law.

For more information, please contact:

For AMTD IDEA Group:
IR Office
AMTD IDEA Group
EMAIL: ir@amtdinc.com

For AMTD Digital Inc.:
IR Office
AMTD Digital Inc.
EMAIL: ir@amtdigital.net

For The Generation Essentials Group:
IR Office
The Generation Essentials Group
EMAIL: ir@tge.media

Daily Associated News: DAVOLINK Transforms from Wireless Network Equipment Supplier to AI-Based Robotics Integrated Control Platform Company

– Merging AI robot control and wireless networks… Presenting an impactful vision enabling short- and long-term revenue growth by evolving beyond a simple network equipment supplier into an integrated robot automation control design company

– A strategic move to restore shareholder trust, preempt future industrial markets, and compete through technology convergence

ANYANG, South Korea, Feb. 23, 2026 /PRNewswire/ — DAVOLINK, a network security and solutions specialist, is strategically merging with LoadRunner, a smart factory solutions provider. This move signals its transition beyond being a simple security Wi-Fi equipment supplier to becoming an intelligent communications and security integrated platform company.

Following its recent announcement of plans to strengthen financial soundness, expand transparent IR, and implement shareholder-friendly policies, DAVOLINK has positioned the technological merger with LoadRunner—beyond an MOU—as a core pillar for future growth.

DAVOLINK’s intent to embrace LoadRunner extends beyond simple cooperation or a robotics technology partnership.

LoadRunner possesses a platform and automation robot technology featuring large-scale data processing, AI-based analysis, and automated workflow design capabilities, excelling in real-time event processing and building integrated control environments.

It is already expanding business revenue in industrial settings. It is not merely a company presenting a future robotics vision. This distinct advantage is why DAVOLINK chose to pursue integration with LoadRunner at this critical juncture.

By combining DAVOLINK’s expertise in wireless network design, construction, and operation with LoadRunner’s AI analysis engine and robot integration design, DAVOLINK can expand its architecture to simultaneously encompass network infrastructure and data intelligence.

The core of this merger strategy is ‘Intelligent Integrated Control’. While existing network security environments focused on rule-based detection and post-incident response, applying LoadRunner’s AI analysis system and robot technology enables real-time traffic anomaly detection, threat prediction, and automated response processes.

The vast log, traffic, and terminal data collected at the wireless network edge, linked with the central analysis engine, creates a structure where ultra-low-latency analysis and immediate blocking systems operate simultaneously, making it immediately applicable to industrial sites.

DAVOLINK’s wireless network technology already demonstrates competitive strength in enterprise-grade RF design, large-scale endpoint connectivity, edge computing integration, and high-speed traffic management. When combined with LoadRunner’s AI-powered analytics and robotics-integrated control systems, the network itself evolves beyond simple connectivity into an intelligent decision-making system.

This can extend beyond security threat detection to include network optimization, automatic traffic distribution, and predictive failure management.

The convergence of telecommunications infrastructure and AI-based integrated control systems carries significant structural implications for future industrial markets. Industries such as manufacturing, logistics, smart factories, smart cities, defense, and robotics automation generate massive real-time data from IoT sensors, edge devices, and autonomous systems. These sectors require not just connectivity, but intelligent networks capable of analyzing and orchestrating operations in real time.

DAVOLINK and LoadRunner’s integrated strategy reflects this demand. By combining telecommunications, AI, security, robotics, and integrated control design, the partnership targets both near-term revenue opportunities and long-term platform value creation.

This represents more than a technological upgrade. It is a redefinition of the business model.

Rather than remaining focused on hardware sales, DAVOLINK intends to transition toward a platform-as-a-service structure. Following initial network deployment, recurring revenue can be generated through ongoing monitoring services, data analytics subscriptions, and robotics-integrated control system operations.

From an investor perspective, this shift introduces both short-term performance potential and long-term platform scalability as key valuation drivers.

A DAVOLINK executive described the phased integration strategy with LoadRunner as a strategic inflection point that goes beyond technical cooperation to secure global competitiveness for both companies.

Market analysts interpret this as an effort to restore shareholder confidence while presenting a clearly defined growth roadmap. The combination of financial stabilization initiatives and platform expansion strategy reflects a dual-track approach aimed at operational restructuring and future market leadership.

Ultimately, the integration signals DAVOLINK’s evolution from a network infrastructure company into an AI-driven intelligent security and robotics-integrated control platform provider.

As network infrastructure and data intelligence converge, DAVOLINK may position itself as a core infrastructure player within the future robotics and automation ecosystem. Industry experts suggest this strategic move represents a structural transformation designed to secure differentiated global competitiveness through technological convergence.

The company acknowledges investor concerns and has stated its intention to restore trust through transparent execution while simultaneously reshaping its long-term industrial positioning.

By expanding telecommunications capabilities into robotics automation design and integrated control systems, DAVOLINK is presenting what it describes as a realistic, high-impact future technology vision capable of generating both short-term and long-term revenue streams.

With the LoadRunner MOU, DAVOLINK has signaled renewed strategic momentum. Robotics industry analysts view the partnership as symbolically and structurally significant, marking the company’s entry into intelligent robotics-integrated control system design and operations.

iRegene Hits Dual Global Firsts: U.S. Patient Dosed in Phase IIa for NouvNeu001 in Parkinson’s and First Enrollment in China’s Randomized MSA Trial for NouvNeu004

CHENGDU, China, Feb. 23, 2026 /PRNewswire/ — The global race to treat neurodegenerative diseases has reached a new tempo as iRegene Therapeutics pushes its cell therapy pipeline into key clinical stages in the U.S. and China. Concurrently, the company’s “AI + Chemical Induction” platform saw its first U.S. patient dosed for Parkinson’s disease at Weill Cornell Medical Center and its first patient enrolled for Multiple System Atrophy (MSA) at Beijing Tiantan Hospital. These parallel milestones for NouvNeu001 and NouvNeu004 represent the next phase of iRegene’s global strategy, transitioning from early safety data into mid-stage clinical trials designed to rigorously evaluate therapeutic efficacy across international patient cohorts.

First Patient Dosed in U.S. Phase IIa Trial of NouvNeu001 for Parkinson‘s Disease

NouvNeu001 is an investigational off-the-shelf cell therapy derived from induced pluripotent stem cells (iPSCs) and chemically induced into dopaminergic progenitor cells. The therapy was administered via stereotactic neurosurgery into the bilateral putamen at Weill Cornell Medical Center in the first patient of an open-label U.S. Phase II study.

Building on positive Phase I data, the U.S. Food and Drug Administration (FDA) cleared NouvNeu001 for direct Phase II entry in the Q3 2025, following Fast Track Designation (FTD) and Regenerative Medicine Advanced Therapy (RMAT) designation. This progression validates iRegene’s preclinical and clinical package and robust CMC framework, enabling closer FDA collaboration and accelerated pathways.

NouvNeu001 is designed to address the underlying pathology of Parkinson’s disease by replacing lost dopaminergic neurons and modifying disease progression — a “single dose, sustained benefit” approach aimed at addressing critical unmet needs. With the first patient dosed in U.S., parallel Phase II trials continue in both the U.S. and China.

First Patient Enrolled in China for MSA Trial with NouvNeu004

In parallel, iRegene has enrolled the first patient in a randomized controlled clinical trial in China evaluating NouvNeu004, its allogeneic iPSC-derived off-the-shelf cell therapy candidate for Multiple System Atrophy (MSA). Led by Principal Investigator Professor Yilong Wang at Beijing Tiantan Hospital, Capital Medical University, the study marks a significant advancement for MSA – a rapidly progressive neurodegenerative disorder with no approved disease-modifying therapies.

NouvNeu004 employs a dual “neurotrophic support + neural reconstruction” strategy, providing trophic support to affected brain regions while promoting functional neural differentiation to potentially halt or reverse progression. China’s NMPA approved the integrated Phases I–III trial application in October 2025, while the U.S. FDA has granted a special exemption and cleared an international Phase I trial, enabling efficient simultaneous development in both countries.

“Dosing the first U.S. patient for Parkinson’s disease and enrolling the first MSA patient in China are pivotal milestones in our mission to deliver transformative, disease-modifying therapies to patients worldwide,” said Dr. Meng Cai, Chief Medical Officer of iRegene Therapeutics.

“These parallel advances reflect the productivity of our ‘AI + Chemical Induction’ platform, yielding two pioneering ‘off-the-shelf’ cell therapies: NouvNeu001 for Parkinson’s disease and NouvNeu004 for Multiple System Atrophy. Together, they demonstrate our commitment to a robust global development pathway and our continued contribution to the advancement of cell therapy for neurodegenerative diseases.”

The “AI + Chemical Induction” Advantage: From Proof-of-Concept to Industrial Validation

iRegene’s core strategy centers on its proprietary “AI + Chemical Induction” platform, engineered to bring scalability and consistency to cell therapy manufacturing. While traditional differentiation methods frequently rely on complex growth factors and commercial media cocktails – which are often prone to batch-to-batch variability and high costs – iRegene utilizes algorithm-optimized small molecule combinations to direct cellular differentiation toward specific lineages.

This chemical induction approach is designed to reduce batch-to-batch variability and support consistent manufacturing under a stable CMC framework, facilitating true off-the-shelf production at lower costs with reduced supply chain complexity compared to personalized or growth factor-dependent therapies. The platform’s foundational technology has been granted patents across China, Japan, and the U.S.

Building on this foundation, iRegene is developing a pipeline of universal, iPSC-derived cell therapies for currently incurable diseases, led by its flagship program and several novel candidates:

  • NouvNeu001 for Parkinson‘s disease – The world’s first clinical-stage, allogeneic iPSC-derived, chemically induced dopaminergic progenitor cell therapy for PD; holds dual FDA FTD (August 2025) and RMAT (December 2025) designations; IND cleared in both China and the U.S.; now in Phase II trials in both China and the U.S.
  • NouvNeu003 for early-onset Parkinson‘s disease – The company’s second product candidate. IND approved by China’s NMPA (December 2023); Phase I completed in China.
  • NouvNeu004 for Multiple System Atrophy – World’s first “AI + Chemical Induction”-derived cell therapy to enter clinical development for MSA; IND approved by China NMPA covering Phases I–III; U.S. FDA special exemption and international Phase cleared; first patient enrolled in China randomized trial.
  • NouvSight001 for Retinal Degenerative Diseases (RDDs) – U.S. FDA Orphan Drug Designation granted (March 2024); advancing as an innovative ophthalmology therapy.

This expanding pipeline underscores the versatility of iRegene’s underlying technology, demonstrating the platform’s capacity to deliver a new generation of scalable cell therapies for complex neurodegenerative disorders. As these candidates move into advanced clinical stages, they represent a tangible shift toward establishing chemically induced iPSC-derived treatments as a safe and effective pillar of global regenerative medicine.

About iRegene Therapeutics

Founded in 2017 by a team of international professionals, iRegene Therapeutics is a pioneer in applying “Chemical Induction” to precisely reprogram cell fate and optimize cellular functions for innovative cell therapies. Leveraging its proprietary “AI + Chemical Induction” platform, iRegene has built a robust pipeline targeting currently incurable diseases, including Parkinson’s disease and Multiple System Atrophy.