TAMPA, FLA., Mar 23, 2026 - (ACN Newswire via SeaPRwire.com) - Wellgistics Health, Inc. ("Wellgistics" or the "Company") (NASDAQ:WGRX) today announced that it has entered into a non-exclusive, non-binding Letter of Intent ("LOI") to evaluate a potential acquisition of Neuritek Therapeutics, a neuroscience-focused research organization.The proposed all stock transaction, if completed, is intended to enhance Wellgistics' existing revenue-generating healthcare platform by expanding capabilities adjacent to its core technology-enabled pharmacy distribution and services business. Through its integrated ecosystem spanning prescription fulfillment, wholesale distribution, and AI-driven patient access solutions, Wellgistics connects manufacturers, providers, and a nationwide network of independent pharmacies. The Company believes that adding a research-focused organization could strengthen alignment between drug development and commercialization, enabling earlier engagement with pharmaceutical partners, improving pipeline visibility, and supporting incremental revenue opportunities while enhancing long-term shareholder value through a more integrated and differentiated platform.The transaction remains subject to the completion of due diligence, negotiation and execution of definitive agreements, approval by the boards of directors of the respective parties, and other customary closing conditions. There can be no assurance that a definitive agreement will be entered into or that the proposed transaction will be consummated on the terms currently contemplated, or at all. The LOI is non-binding and does not obligate either party to complete the proposed transaction. The scope, structure, and terms of any potential transaction remain under evaluation and may change materially as a result of ongoing diligence and negotiations.The Company is also actively evaluating additional strategic opportunities across the healthcare and life science sectors as part of its broader growth strategy. These opportunities may include acquisitions, partnerships, or other strategic transactions. There can be no assurance that any such initiatives will result in completed transactions.About Wellgistics Health, IncWellgistics Health is a rapidly scaling, technology-driven healthcare platform positioned at the center of pharmaceutical distribution and patient access. The Company has built an integrated, high-performance ecosystem spanning wholesale distribution, prescription fulfillment, and AI-powered access solutions, directly connecting pharmaceutical manufacturers, healthcare providers, and a nationwide network of independent pharmacies.By combining infrastructure, data, and intelligent automation, Wellgistics is executing on a capital-efficient model designed to capture significant share in large and fragmented healthcare markets. The Company is focused on expanding high-margin revenue streams, deepening strategic manufacturer relationships, and driving operating leverage across its platform. With a differentiated end-to-end offering and disciplined execution, Wellgistics is positioned to accelerate growth, enhance earnings visibility, and deliver outsized long-term value for shareholders.About Neuritek Therapeutics Inc.Neuritek Therapeutics Inc. has developed a next-generation bio-mechanism based treatment, treating the root cause of Post-Traumatic Stress Disorder (PTSD). Neuritek's first to market treatment is an orally active inhibitor of fatty acid amide hydrolase type 1 (FAAH1), the enzyme responsible for metabolizing anandamide (AEA) and the first mechanisms-based treatment for PTSD. The company was founded by Doctor William Hapworth MD., a pioneer in clinical research and a practicing psychiatrist with over 30 years' experience.Learn more at www.neuritek.com or join the conversation at LinkedIn, neuritek-therapeutics-incForward-Looking StatementsThis press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and other applicable federal securities laws. These forward-looking statements include, without limitation, statements regarding: the potential acquisition of Neuritek Therapeutics, Inc. ("Neuritek"), including the anticipated structure, valuation, timing, and likelihood of completion of any transaction; the preliminary and non-binding nature of the letter of intent; the potential strategic, operational, and financial benefits of any such transaction; the Company's ability to negotiate and enter into definitive agreements; the Company's ability to obtain any required financing; the integration of any acquired business; and the Company's broader growth strategy and future performance.Forward-looking statements may be identified by words such as "may," "could," "would," "should," "expect," "anticipate," "believe," "intend," "plan," "project," "estimate," "potential," "opportunity," "target," "forecast," "continue," "will," and similar expressions.These forward-looking statements are based on current expectations, assumptions, and estimates and are subject to significant risks and uncertainties, many of which are beyond the Company's control. Important factors that could cause actual results to differ materially include, but are not limited to: the risk that the parties do not enter into definitive agreements; the risk that the letter of intent is terminated or does not result in a completed transaction; uncertainties related to the preliminary nature of the proposed valuation and transaction terms, which may change materially; the risk that any required financing is not obtained on acceptable terms or at all; the risk that anticipated benefits of any transaction are not realized; risks associated with integrating a research-focused organization into the Company's existing business; risks related to the development, testing, regulatory approval, and commercialization of pharmaceutical or therapeutic products, including the possibility of unfavorable clinical results or delays; regulatory and compliance risks; and other risks and uncertainties described from time to time in the Company's filings with the U.S. Securities and Exchange Commission.Forward-looking statements speak only as of the date they are made, and undue reliance should not be placed on such statements. The Company undertakes no obligation to update or revise any forward-looking statements, except as required by applicable law.Wellgistics Media & Investor ContactMedia: media@wellgisticshealth.comInvestor Relations: IR@wellgisticshealth.comSOURCE: Wellgistics Health, Inc. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

佛罗里达州坦帕市, 2026年3月23日 - (亚太商讯 via SeaPRwire.com) - Wellgistics Health, Inc.（“Wellgistics”或“公司”）（纳斯达克代码：WGRX）今日宣布，已签署一份非独家、非约束性的意向书（“LOI”），旨在评估潜在收购专注于神经科学研究的机构Neuritek Therapeutics。若该拟议的全股票交易得以完成，旨在通过扩展其核心技术驱动的药品分销及服务业务周边能力，从而增强Wellgistics现有的创收医疗保健平台。通过其涵盖处方配药、批发分销及人工智能驱动的患者就医解决方案的集成生态系统，Wellgistics将制造商、医疗服务提供者以及遍布全国的独立药房网络紧密连接起来。公司认为，引入一家以研究为导向的机构，将有助于加强药物研发与商业化之间的协同，从而实现与制药合作伙伴的早期对接，提高产品管线透明度，并创造增量收入机会；同时，通过构建更集成、更具差异化的平台，提升长期股东价值。该交易仍需完成尽职调查、最终协议的谈判与签署、各方董事会批准以及满足其他惯常的交割条件。无法保证最终协议将得以签署，亦无法保证拟议交易将按当前设想的条款完成，甚至可能无法完成。该意向书不具约束力，且不强制任何一方完成拟议交易。任何潜在交易的范围、结构及条款仍在评估中，并可能因持续进行的尽职调查和谈判而发生重大变化。作为更广泛增长战略的一部分，本公司亦正在积极评估医疗保健及生命科学领域的其他战略机遇。这些机遇可能包括收购、合作或其他战略交易。无法保证此类举措将最终促成交易。关于 Wellgistics Health, IncWellgistics Health 是一家快速扩张、技术驱动的医疗保健平台，立足于药品分销与患者获取服务的核心位置。公司已构建了一个涵盖批发分销、处方配药及人工智能驱动的获取解决方案的集成化、高性能生态系统，直接连接制药商、医疗服务提供商以及覆盖全美的独立药房网络。通过整合基础设施、数据和智能自动化，Wellgistics正实施一种资本高效的运营模式，旨在在庞大且分散的医疗保健市场中占据显著份额。公司致力于拓展高利润率收入来源、深化与制造商的战略合作关系，并在整个平台推动运营杠杆效应。凭借差异化的端到端服务和严谨的执行力，Wellgistics 已做好准备加速增长、提升盈利可见度，并为股东创造超额的长期价值。关于 Neuritek Therapeutics Inc.Neuritek Therapeutics Inc. 开发了一种基于生物机制的下一代疗法，旨在治疗创伤后应激障碍（PTSD）的根本原因。Neuritek 率先上市的疗法是一种口服活性脂肪酸酰胺水解酶 1 型（FAAH1）抑制剂，该酶负责代谢内源性大麻素（AEA），这是首个基于机制的 PTSD 治疗方案。 该公司由威廉·哈普沃斯（William Hapworth）医学博士创立，他不仅是临床研究领域的先驱，还是一位拥有30多年临床经验的执业精神科医生。了解更多信息请访问 www.neuritek.com ，或在 LinkedIn 关注 neuritek-therapeutics-inc 参与讨论前瞻性陈述本新闻稿包含《1995年私人证券诉讼改革法案》及其他适用联邦证券法所界定的前瞻性陈述。这些前瞻性陈述包括但不限于以下内容：关于潜在收购Neuritek Therapeutics, Inc.（“Neuritek”）的陈述，包括任何交易的预期结构、估值、时间安排及完成可能性；意向书的初步性和非约束性；此类交易可能带来的战略、运营及财务效益； 本公司协商并签订最终协议的能力；本公司获取任何必要融资的能力；任何被收购业务的整合；以及本公司的整体增长战略和未来业绩。前瞻性陈述可通过“可能”、“可能”、“将会”、“应该”、“预期”、“预计”、“相信”、“打算”、“计划”、“预测”、“估计”、“潜在” “机会”、“目标”、“预测”、“继续”、“将”以及类似表述。这些前瞻性陈述基于当前的预期、假设和估计，并受重大风险和不确定性的影响，其中许多因素超出本公司的控制范围。可能导致实际结果与预期存在重大差异的重要因素包括但不限于：各方未能签订最终协议的风险；意向书被终止或未能促成交易完成的风险；拟议估值及交易条款仅为初步性质且可能发生重大变化的不确定性；未能以可接受的条款获得所需融资或根本无法获得融资的风险； 任何交易预期收益未能实现的风险；将以研发为主的组织整合至本公司现有业务的相关风险；药品或治疗产品的开发、测试、监管审批及商业化相关风险，包括临床结果不佳或出现延误的可能性；监管及合规风险；以及本公司不时向美国证券交易委员会提交的文件中所述的其他风险和不确定性。前瞻性陈述仅反映其作出之日的观点，不应过度依赖此类陈述。除适用法律要求外，本公司不承担更新或修订任何前瞻性陈述的义务。Wellgistics 媒体与投资者联系方式媒体：media@wellgisticshealth.com 投资者关系： IR@wellgisticshealth.com 来源：Wellgistics Health, Inc. Copyright 2026 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

Key Results Highlights:- Revenue Growth: 8.6% increase to approximately HK$1,813.8 million- Net Profit Increase: 3.5% rise to HK$318.1 million, driven by operational efficiency- Final Dividend: Proposed final dividend of HK7.0 cents per share, bringing total dividend for 2025 to HK14.0 cents per share, a 16.7% surge from HK12.0 cents in 2024- Net Cash & Cash Equivalents: HK$782.7 million (HK$557.2 million as at 31st December 2024)Regulatory Milestones:- NMPA Approval: Multi-dose Diquafosol Sodium Eye Drops approved in July 2025; multi-dose Sodium Hyaluronate Eye Drops approved in January 2026 for registration and commercialisation in the PRC- BLA Acceptance: Bevacizumab ophthalmic injection BLA accepted by NMPA in August 2025, marking a crucial regulatory milestoneBusiness Developments:- Exclusive Distribution (Seefunge): Exclusive distribution of Seefunge's Emedastine Difumarate and Oxybuprocaine Hydrochloride Eye Drops in the PRC- Exclusive Distribution (Osteopore): Exclusive distribution of Osteopore’s innovative dental, orthodontic and maxillofacial products in the PRC, Hong Kong and Macau.- Collaboration with Airdoc: Joint operation of Artificial Intelligence-based retinal businesses in the PRC- Strategic Collaboration with Kenvue: Promotion and marketing of Kenvue's consumer health products (Rhinocort(R), Motrin(R), Tylenol(R)) in the PRC.- International Innovation Accelerator: Signed MOU with Suzhou Industrial Park to launch cross-border life sciences accelerator.- First Overseas Market Entry: Beifushu(R) introduced to Singapore via Special Access Route at Singapore National Eye Centre.Intellectual Property and Market Presence:- Robust IP Portfolio: 121 patent certificates or authorisation letters, comprising 91 invention patents, 15 utility model patents and 15 design patents.- Extensive Distribution Network: Products available in over 14,600 hospitals and medical providers, and approximately 2,600 pharmaceutical stores across the PRCAwards and Recognition:- 2025 Top 500 Manufacturing Companies in Guangdong Province: Recognises industrial scale and comprehensive competitiveness- National Manufacturing Champion Enterprise: Affirms leading position in specialized biopharmaceutical segment- 2025 "Golden Kunpeng" China Financial Value Ranking – Most Valuable Listed Company for Investment: Highlights capital market recognition of growth potential- Participation at Asia-Pacific Academy of Ophthalmology Congress 2026: Showcasing key ophthalmology products and pipeline assets, strengthening engagement with regional eye care professionals and institutions.HONG KONG, Mar 23, 2026 - (ACN Newswire via SeaPRwire.com) - Essex Bio-Technology Limited (“Essex” and its subsidiary the “Group”, Stock Code: 1061.HK), a leading biologic Group that develops, manufactures and commercialises genetically engineered therapeutic recombinant bovine basic fibroblast growth factor (“rb-bFGF”), today announced robust annual results for the year ended 31st December 2025, with revenue up 8.6% to HK$ 1,813.8 million and net profit up 3.5% YoY to HK$318.1 million. The Group achieved multiple regulatory milestones and expanded its product portfolio through strategic collaborations, and Beifushu’s landmark entry into Singapore. These achievements underscore Essex's commitment to innovation and operational excellence, driving sustained revenue and profit growth.Diversified Growth Fueled by Flagship BiologicsThe Group achieved a consolidated turnover of approximately HK$1,813.8 million, with an increase of 8.6% as compared to approximately HK$1,669.8 million in 2024. Correspondingly, the Group’s profit increased by 3.5% to approximately HK$318.1 million as compared to approximately HK$307.2 million in 2024.The Beifushu(R) series and Beifuji(R) series, the Group’s flagship products drove growth, contributing 83.5% of turnover.The ophthalmology segment (“Ophthalmology”) recorded a turnover of HK$835.0 million, grew 8.2% year-on-year, led by Beifushu(R) unit-dose eye drops and supported by its preservative free design and expanding application scenarios, which cover multiple areas such as dry eye treatment and post-operative recovery, and contributions from Beifushu(R) eye gel, (Iodized Lecithin Capsules) and a range of unit-dose eye drops (Tobramycin, Levofloxacin, Sodium Hyaluronate, Moxifloxacin Hydrochloride and Diquafosol Sodium Eye Drops).The surgical segment (“Surgical”) turnover rose 1.8% year-on-year to HK$895.9 million, leveraging Beifuji’s broad clinical applications across multiple medical departments and strong market presence. It is also supported by numerous clinical guidelines and expert consensus, thereby laying a solid foundation for future indication expansion and sustained growth. In addition, Group Carisolv(R) dental caries removal gel, PELNACTM collagen-based artificial dermis and SCALGENTM double-layered artificial dermis had further strengthened and contributed to the Surgical business.Notably, Healthcare and Partner Services delivered a total turnover of approximately HK$82.9 million for the year ended 31st December 2025, representing a significant increase of 350% as compared to 2024. The growth was primarily driven by Dr. YaDian oral care products, online and offline healthcare services and CMO/CDMO services.Strengthening Financial Position and Shareholder ReturnsThe Group maintains a healthy financial position, with cash and cash equivalents of approximately HK$782.7 million as of 31st December 2025. Bank borrowings stand at HK$325.6 million, with a manageable repayment schedule over 5 years period. The Group’s gearing ratio is at 30.9% (2024: 28.8%), indicating disciplined financial management and ample liquidity.The Board is pleased to propose a final dividend of HK7.0 cents per ordinary share. Together with the interim dividend of HK7.0 cents per ordinary share, the total dividend for 2025 reaches HK14.0 cents, representing a notable year-on-year increase of 16.7% from HK12.0 cents in 2024, demonstrating the Group’s ongoing commitment to delivering greater returns to its shareholders.Broad Portfolio and Robust Pipeline Fuel Sustained GrowthThe Group’s business comprises three core segments: Ophthalmology, Surgical (wound care and healing) and Healthcare and Partner Services segment, with the Group’s six (6) flagship commercialised biologics, collectively referred to as the “bFGF Series”, which are marketed and sold in the PRC. Three of the bFGF Series were approved by NMPA as Category I drugs, and five are listed on the National Drug List for Basic Medical Insurance, Work-Related Injury Insurance and Maternity Insurance in the PRC.In addition, the Group offers a portfolio of commercialised preservative-free unit-dose eye drops, including Tobramycin, Levofloxacin, Sodium Hyaluronate, Moxifloxacin Hydrochloride and Diquafosol Sodium Eye Drops. The Group further expanded its ophthalmology franchise by obtaining NMPA approvals for the registration and commercialisation of multi-dose Diquafosol Sodium Eye Drops in July 2025 and multi-dose Sodium Hyaluronate Eye Drops in January 2026. The new launches target the PRC’s growing dry eye treatment market, complementing the Group’s Beifushu(R) ophthalmic repair series.As for the Surgical segment, the Group’s Carisolv(R) dental caries removal gel, Portable Ultraviolet Phototherapy Devices, PELNACTM collagen-based artificial dermis, SCALGENTM double-layered artificial dermis and Osteopore’s bioresorbable implants (Osteomesh(R) and Osteoplug(R)), are complementing the Group’s Beifuji(R) wound healing series.Strategic R&D Investment to Capture Emerging Market OpportunitiesThe Group is committed to pragmatically investing in new products and technologies to strengthen its product and R&D pipeline, with a mission to develop groundbreaking therapeutics that address unmet clinical and commercial needs. In 2025, total R&D expenditures were approximately HK$177.2 million, representing 9.8% of the turnover, of which approximately HK$139.3 million were capitalised.During the year, the Group’s Medical Scar Repair Gel obtained NMPA registration approval as a Class II medical device, expanding the Group’s footprint in the fast-growing high-end wound care and medical aesthetics markets, unlocking new growth drivers for long-term success.The global phase 3 clinical project of bevacizumab ophthalmic injection (EB12-20145P) has successfully completed patient enrolment across the PRC, Australia, European Union countries and the United States, with the last patient last visit was completed. A Biologics License Application (BLA) was accepted by NMPA in the PRC in August 2025.To amplify the Group’s presence in the Asia ophthalmic community and accelerate the market launch of new products, the Group participated in the 2026 Asia-Pacific Academy of Ophthalmology (APAO) Congress. The event provided a premium platform to showcase ophthalmic solutions, engage with regional clinical experts and partners, and build momentum for the rollout of its innovative ophthalmic products, reinforcing its global brand influence.The Group holds a total of 121 patent certificates or authorisation letters, comprising 91 invention patents, 15 utility model patents and 15 design patents.The Group currently has multiple R&D sites located in Zhuhai (PRC), Boston (United States), London (United Kingdom) and Singapore. These sites support the Group’s efforts to develop new therapeutics and recruit global talent.To date, the Group has 18 R&D programmes ranging from pre-clinical to clinical stages, with several ophthalmology programs currently in the clinical stage, specifically Bevacizumab intravitreal injection, SkQ1 eye drops and Cyclosporine eye dropsBroadening Commercial Reach Through Market Expansion and PartnershipsAs of 31st December 2025, the Group maintains an extensive network of 47 regional sales offices in the PRC and a strategic base in Singapore to facilitate market access into Southeast Asian countries. With a vast distribution network, the Group’s products are prescribed in more than 14,600 hospitals and medical providers, coupled with approximately 2,600 pharmaceutical stores, covering major cities throughout the PRC.During the year under review, the Group achieved multiple landmark breakthroughs in the PRC and overseas market expansion, unlocking new multi-dimensional growth momentum. In the overseas market, the Group’s flagship product Beifushu(R) was successfully introduced to Singapore via the Special Access Route at the Singapore National Eye Centre, marking the product’s first commercial launch beyond the PRC, and establishing a solid foothold to support the Group’s future expansion into Southeast Asia and global markets.In the PRC market, the Group entered into two landmark strategic partnerships during the year: a collaboration with global consumer health leader Kenvue, under which the Group will leverage its extensive nationwide commercial network in the PRC to carry out promotion, medical education and marketing for Kenvue’s selected consumer health products including Rhinocort(R) (Budesonide Nasal Spray), Motrin(R) (Ibuprofen Suspension/Drops), and Tylenol(R) (Paracetamol Drops/Suspension); and an exclusive distribution agreement for Osteopore’s innovative dental, orthodontic and maxillofacial products in the PRC, Hong Kong and Macau, marking a strategic entry into the high-potential stomatology market. The partnerships broaden the Group’s healthcare business footprint, delivering strong synergies with its existing ophthalmology and regenerative medicine lines.To drive sustainable growth and expansion for its current and future products, the Group has been investing relentlessly in enhancing its competitiveness and broadening its reach by expanding the clinical indications for its commercialised products, increasing patient access in lower-tier cities across the PRC, developing complementary sales channels, and nurturing the healthtech e-platform to enhance patient access.The Group’s second factory at Zhuhai Hi-Tech Industrial Park, with a gross floor area of about 58,000 square meters for R&D, manufacturing, office and dormitory, is expected to complete in the period of 2026 -2027.Mr. Patrick Ngiam, Chairman of Essex, said “2025 was a standout year with Beifushu’s landmark entry into Singapore, driving robust growth through flagship products, innovation-focused R&D, and strategic partnerships. Essex remains committed to addressing unmet needs and driving long-term growth.We will proactively and systematically recalibrate operating and distribution costs to mitigate the negative impact on FY26 profit from the increase of VAT from 3% to 13% without disrupting our focus on Group development plans.”About EssexBio (1061.HK)EssexBio is a bio-pharmaceutical company that develops, manufactures, and commercialises genetically engineered therapeutic b-bFGF, with six commercialised biologics currently marketed in China. Additionally, the Company has a diverse portfolio of commercialised preservative-free unit-dose eye drops, Shilishun (Iodized Lecithin Capsules) and others, which are principally prescribed for wound healing and diseases in Ophthalmology and Dermatology. These products are marketed and sold through approximately 14,600 hospitals, supported by the Company’s 47 regional offices in China. Leveraging its in-house R&D platform in growth factor and antibody technology, EssexBio maintains a robust pipeline of projects in various clinical stages, covering a wide range of fields and indications. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

Brisbane, Australia--(ACN Newswire via SeaPRwire.com - March 23, 2026) - Graphene Manufacturing Group Ltd (TSXV: GMG) (OTCQX: GMGMF) ("GMG" or the "Company") is pleased to announce that the Company has officially launched its European sales activity. During the week of March 9th, GMG held a kick off training workshop in London where it brought together its new team members from various locations in Europe and UK for technical product and sales training.The GMG European Sales team numbers more than 10 professional sales executives based in Europe and UK who focus on lead generation, inside sales and executive sales business development for GMG's G® Lubricant and THERMAL-XR® products.Figure 1: Members of the GMG European Sales TeamTo view an enhanced version of this graphic, please visit:https://images.newsfilecorp.com/files/8082/289529_gmg_figure1.jpgSeparately, the Company is also pleased to announce that it has been informed that the G® Lubricant patent in Europe has been accepted to be granted for a period of 20 years.Craig Nicol, CEO & Managing Director of the Company, commented "Building a sales force in key areas of the world is one of GMG's key activities it is focused on right now and to get the European team set up and running so fast has been a great achievement."Jack Perkowski, Chairman and Non-Executive Director of the Company, commented: "I congratulate the Company on building the European Sales team and look forward to hearing of future success."About GMG:GMG is an Australian based clean-technology company which develops, makes and sells energy saving and energy storage solutions, enabled by graphene manufactured via in house production process. GMG uses its own proprietary production process to decompose natural gas (i.e. methane) into its natural elements, carbon (as graphene), hydrogen and some residual hydrocarbon gases. This process produces high quality, low cost, scalable, 'tuneable' and low/no contaminant graphene suitable for use in clean-technology and other applications.The Company's present focus is to de-risk and develop commercial scale-up capabilities, and secure market applications. In the energy savings segment, GMG has initially focused on graphene enhanced heating, ventilation and air conditioning ("HVAC-R") coating (or energy-saving coating) which is now being marketed into other applications including electronic heat sinks, industrial process plants and data centres. Another product GMG has developed is the graphene lubricant additive focused on saving liquid fuels initially for diesel engines.In the energy storage segment, GMG and the University of Queensland are working collaboratively with financial support from the Australian Government to progress R&D and commercialization of graphene aluminium-ion batteries ("G+AI Batteries"). GMG has also developed a graphene additive slurry that is aimed at improving the performance of lithium-ion batteries.GMG's 4 critical business objectives are:Produce Graphene and improve/scale cell production processesBuild Revenue from Energy Savings ProductsDevelop Next-Generation BatteryDevelop Supply Chain, Partners & Project Execution CapabilityFor further information please contact:Craig Nicol, Chief Executive Officer & Managing Director of the Company at craig.nicol@graphenemg.com, +61 415 445 223Leo Karabelas at Focus Communications Investor Relations, leo@fcir.ca, +1 647 689 6041Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accept responsibility for the adequacy or accuracy of this news release.Cautionary Note Regarding Forward-Looking StatementsThis news release includes certain statements and information that may constitute forward-looking information within the meaning of applicable Canadian and U.S. securities laws. Forward-looking statements relate to future events or future performance and reflect the expectations or beliefs of management of the Company regarding future events. Generally, forward-looking statements and information can be identified by the use of forward-looking terminology such as "intends", "believes" "expects" or "anticipates", or variations of such words and phrases or statements that certain actions, events or results "may", "could", "should", "would" or will "potentially" or "likely" occur. This information and these statements, referred to herein as "forward‐looking statements", are not historical facts, are made as of the date of this news release and include without limitation, the size, term and success of GMG's European sales team and the eventual granting of and successful enforceability of the Company's G® Lubricant patent.Such forward-looking statements are based on a number of assumptions of management, including the European sales team will perform and the Company's G® Lubricant patent will be patented successfully. Additionally, forward-looking information involves a variety of known and unknown risks, uncertainties and other factors which may cause the actual plans, intentions, activities, results, performance or achievements of GMG to be materially different from any future plans, intentions, activities, results, performance or achievements expressed or implied by such forward-looking statements. Such risks include, without limitation that the GMG European Sales team does not successfully drive sales for the Company and the Company's G® Lubricant patent is not patented and the risk factors set out under the heading "Risk Factors" in the Company's annual information form dated November 4, 2025 available for review on the Company's profile at www.sedarplus.ca.Although management of the Company has attempted to identify important factors that could cause actual results to differ materially from those contained in forward-looking statements or forward-looking information, there may be other factors that cause results not to be as anticipated, estimated or intended. There can be no assurance that such statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking statements and forward-looking information. Readers are cautioned that reliance on such information may not be appropriate for other purposes. The Company does not undertake to update any forward-looking statement, forward-looking information or financial out-look that are incorporated by reference herein, except in accordance with applicable securities laws.To view the source version of this press release, please visit https://www.newsfilecorp.com/release/289529 Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

关键业绩摘要：- 收入增长：收入同比增长8.6%至约18.14亿港元- 净利润提升：得益于运营效率，净利润增长3.5%至3.18亿港元- 末期股息：拟派末期股息每股0.07港元，2025年全年股息达每股0.14港元，较2024年全年股息的每股0.12港元大幅增加16.7%- 现金及现金等价物：7.83亿港元（2024年12月31日：5.57亿港元）研发里程碑：- NMPA批准：多剂量地夸磷索钠滴眼液于2025年7月获批；多剂量玻璃酸钠滴眼液于2026年1月获批在中国注册和商业化。- BLA受理：贝伐珠单抗眼内注射液的生物制品许可申请（BLA）于2025年8月获NMPA受理，标志着重要的监管里程碑。商业发展：- 独家代理（视方极）：获得浙江视方极富马酸依美斯汀滴眼液、盐酸奥布卡因滴眼液的独家代理权。- 独家代理（Osteopore）：获得Osteopore创新的牙科、正畸及颌面产品在中国内地、香港及澳门的独家代理权。- 与鹰瞳科技合作：在中国实现眼底AI业务的联合运营。- 与科赴战略合作：在中国推广及营销科赴的消费者健康产品（雷诺考特(R)、美林(R)、泰诺林(R)）。- 国际创新加速器：与苏州工业园区签订战略合作谅解备忘录，推出国际创新加速器。- 首个海外市场准入：贝复舒(R)通过特别采用程序成功引入新加坡国家眼科中心。知识产权与市场布局：- 强大的知识产权组合：持有合共121份专利证书或授权书，包括91项发明专利、15项实用新型专利及15项外观专利。- 广泛的销售网络：产品覆盖中国内地超14,600家医院和医疗机构以及约2,600家药房。奖项与荣誉：- 2025年广东省制造业企业500强：表彰产业规模及综合竞争力- 国家级制造业单项冠军企业：确认在专业生物制药领域的领先地位- 2025"金鲲鹏"中国财经价值榜－最具投资价值上市公司：突显资本市场对增长潜力的认可- 参与2026年亚太眼科学会大会：展示主要眼科产品及在研管线，加强与区域眼科专业人士及机构的联系。香港, 2026年3月23日 - (亚太商讯 via SeaPRwire.com) - 亿胜生物科技有限公司（"亿胜生物"及其附属公司"集团"；股份代号：1061.HK），一家领先的生物制药企业，专注于研发、生产和销售基因工程药物重组牛碱性成纤维细胞生长因子（"rb-bFGF"），今日公布截至2025年12月31日止的强劲年度业绩。集团收入同比增长8.6%至18.14亿港元，利润同比增长3.5%至3.18亿港元。年内，亿胜生物达成了多项监管里程碑，并通过战略合作扩大了产品组合，同时成功将贝复舒(R)引入新加坡。这些成就彰显了亿胜对创新和卓越运营的承诺，持续推动收入和利润的增长势头。旗舰生物药推动多元化增长集团实现综合营业额约18.14亿港元，较2024年的约16.70亿港元增长8.6%。相应地，集团溢利较2024年的约3.07亿港元增长3.5%至约3.18亿港元。集团的旗舰产品贝复舒(R)系列及贝复济(R)系列持续带动增长，占总营业额的83.5%。眼科分部录得营业额8.35亿港元，同比大幅增长8.2%。其中，单剂量贝复舒(R)滴眼液凭借无防腐剂设计及应用场景的持续拓展（覆盖干眼症治疗及术后修复等多元领域）实现强劲销售增长，贝复舒(R)眼用凝胶、适丽顺(R)（卵磷脂络合碘胶囊）和一系列不含防腐剂单剂量滴眼液（包括妥布霉素、左氧氟沙星、玻璃酸钠、盐酸莫西沙星及地夸磷索钠滴眼液）亦作出持续贡献。外科分部实现营业额8.96亿港元，增长1.8%，主要受惠于贝复济(R)系列产品在多个临床科室的广泛应用及其稳固的市场地位。同时，贝复济(R)系列产品已获多项临床指南及专家共识支持，为未来适应症拓展及持续增长奠定基础。此外，集团的Carisolv(R)龋齿凝胶、皮耐克可吸收性敷料、适可健双层人工真皮修复材料等产品进一步增强并促进了外科业务的发展。值得注意的是，医疗保健及伙伴服务于截至2025年12月31日止年度录得总营业额约8,290万港元，较2024年大幅增长350%。增长主要来源于伢典医生口腔护理产品、线上及线下医疗保健服务及CMO/CDMO服务等。稳健的财务基础和股东回报集团维持稳健的财务状况。截至2025年12月31日，集团录得现金及现金等价物约7.83亿港元。银行借贷为3.26亿港元，将在未来五年内按计划偿还。集团的资产负债比率为30.9%（2024年：28.8%），反映出集团具备严谨的财务管理能力和充足的流动性。董事会欣然建议派发末期股息每股普通股0.07港元。连同中期股息每股普通股0.07港元，2025年全年股息达到0.14港元，较2024年全年股息的0.12港元同比显著增长16.7%，以彰显集团致力于为股东创造价值的承诺。广泛的产品组合及强大的研发管线支持持续增长集团业务由三个核心分部组成：眼科、外科（创伤护理及修复）以及医疗保健及伙伴服务分部。集团拥有六种于中国市场销售的商业化生物制剂，统称"bFGF系列"。其中三种bFGF系列为国家药品监督管理局（"NMPA"）批准的国家一类新药，五种被列入中国国家基本医疗保险、工伤保险和生育保险药品目录。此外，集团提供一系列商业化的不含防腐剂单剂量滴眼液，包括妥布霉素、左氧氟沙星、玻璃酸钠、盐酸莫西沙星及地夸磷索钠滴眼液。集团进一步拓展其眼科产品组合，分别于2025年7月及2026年1月获得NMPA批准多剂量地夸磷索钠滴眼液及多剂量玻璃酸钠滴眼液在中国注册和商业化。新获批产品聚焦于中国不断增长的干眼治疗市场，以补充集团的贝复舒(R)眼表修复系列产品。外科方面，集团的Carisolv(R)龋齿凝胶及伢典医生口腔护理产品，以及一系列产品及医疗器械（包括紫外线光疗仪、皮耐克可吸收性敷料、Osteopore用于牙科手术的生物可吸收植入物（Osteomesh(R)及Osteoplug(R)）及其他用于近视防控的医疗器械），共同补充了集团的贝复济(R)创伤修复系列产品。战略性研发投资以把握新兴市场机遇集团致力于务实地投资新产品及技术，以强化其产品及研发管线，使命是开发解决未满足的临床及商业需求的突破性的疗法。2025年，研发总支出约为1.77亿港元，占营业额的9.8%，其中约1.39亿港元已资本化。年内，集团医用疤痕修复凝胶获批NMPA二类医疗器械注册证，将集团业务拓展至快速增长的高端伤口护理及医疗美容市场，解锁新增长动力以推动长期发展。贝伐珠单抗眼内注射液（EB12-20145P）的全球三期临床项目已成功完成了在中国、澳大利亚、欧盟国家及美国的患者入组，最后一名患者已完成最后一次访视。其生物制品许可申请（BLA）已于2025年8月获中国NMPA受理。为提升集团在亚洲眼科领域的影响力，并加速新产品的市场推出，集团参与了2026年亚太眼科学会（APAO）大会。该会议提供了一个绝佳平台，用以展示眼科解决方案、与区域临床专家和合作伙伴交流，并为集团创新眼科产品的推出积聚动能，从而提升全球品牌影响力。集团持有121份专利证书或授权书，包括91项发明专利、15项实用新型专利及15项外观专利。集团目前于珠海（中国）、波士顿（美国）、伦敦（英国）及新加坡设立多个研发基地。这些基地为集团开发新疗法和招募全球人才提供支援。截至目前，集团共有18项研发计划处于临床前至临床阶段，其中数项眼科项目处于临床阶段，具体包括贝伐珠单抗眼内注射液、SkQ1滴眼液及环孢素滴眼液。透过市场扩张与合作拓宽商业覆盖截至2025年12月31日，集团于中国设有47间地区销售办事处，并于新加坡设有战略基地，以促进其产品进入东南亚市场。凭借庞大的分销网络，集团的治疗产品在中国各地的逾14,600家医院及医疗机构以及约2,600家药房开具处方，覆盖了中国各地的主要城市。回顾年内，集团在国内外市场扩张方面取得了多项里程碑式的突破，解锁了多维度的新增长动力。在海外市场，集团的旗舰产品贝复舒(R)通过特别采用程序成功引入新加坡国家眼科中心，标志着该产品首次进入中国以外地区，为集团未来进军东南亚及全球市场奠定了坚实基础。在国内，集团年内达成了两项具里程碑意义的战略合作：与全球消费者健康领导企业科赴合作，利用集团在中国广泛的全国性商业网络，对科赴精选的消费者健康产品（包括雷诺考特(R)、美林(R)及泰诺林(R)）进行推广、学术教育及营销；以及与Osteopore签订独家分销协议，在中国内地、香港及澳门分销其创新的牙科、正畸及颌面产品，标志着集团战略性进军高潜力的口腔科市场。这些合作拓宽了集团医疗保健业务的版图，并与其现有的眼科及再生医学业务产生强大的协同效应。为推动现有及未来产品的可持续增长和扩张，集团一直不懈地进行投资，通过扩大其商业化产品的临床适应症、增加中国较低线城市的患者可及性、开发补充销售渠道，以及培育医疗科技电子平台以增强患者可及性，来提高其竞争力并拓宽覆盖范围。集团位于珠海高新区科技创新海岸的第二间工厂，建筑面积约58,000平方米，用作研发、生产、办公及宿舍，预计将于2026或2027年间完工。亿胜生物主席严名炽先生表示："2025年对亿胜来说是具有里程碑意义的一年，贝复舒(R)成功引入新加坡，集团亦依托其核心产品、创新研发及战略合作，实现稳健增长。未来，亿胜将继续致力于满足未被满足的临床需求，推动集团长期发展。我们将主动、系统性地优化运营及销售成本，以缓解增值税由3%上调至13%对2026财年利润带来的不利影响，同时保证集团发展规划的稳步推进。"关于亿胜生物（股票代码﹕1061.hk）亿胜生物是一间专注于研发、生产和销售基因工程药物b-bFGF的生物制药企业，拥有包括贝复舒(R)、贝复济(R)、贝复新(R)在内的六种基因工程药物在中国上市销售。此外，公司还拥有包含一系列不含防腐剂单剂量滴眼液和适丽顺(R)卵磷脂络合碘胶囊等的多元化产品组合，主要应用于眼科及皮肤科处方药领域的创伤修复及疾病治疗。这些产品在公司于中国的47个区域办事处的支持下，在逾14,600家医院进行营销和销售。依托自身在生长因子和抗体技术领域的研发平台，亿胜生物在多个临床阶段拥有强大的项目管线，涵盖广泛的领域和适应症。网址: http://www.essexbio.com Copyright 2026 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年3月23日 - (亚太商讯 via SeaPRwire.com) - 云顶新耀宣布与箕星药业香港有限公司（以下简称"箕星药业"）达成资产收购协议 (The Asset Purchase Agreement)，获得艾曲帕米（Etripamil）鼻喷雾剂（拟定中文商品名：星必妥(R)）在大中华区的开发、商业化及产品地产化权益。此次合作是公司深化心血管领域战略布局的重要举措，进一步丰富了公司的产品管线、增强协同效应，持续巩固公司在心血管疾病领域的发展。根据协议，云顶新耀将向箕星药业支付3000万美元（相当于约人民币206,937,000元）首付款，以及最高不超过2000万美元（相当于约人民币137,958,000元）的开发里程碑付款。作为本协议的一部分，云顶新耀将获得箕星药业于2021年5月签订的许可协议及相关附属协议项下的权利、权益、主张、职责、义务及责任（不包括双方约定的部分除外责任）。艾曲帕米鼻喷雾剂是一款新型、速效的钙离子通道阻滞剂，采用便携式鼻喷雾剂给药，起效迅速且耐受性良好，可居家自行使用，可及性高。该药物于2025年12月获得美国食品药品监督管理局（FDA）批准（美国商品名：CARDAMYSTTM），成为30多年来首款且唯一获批用于成人阵发性室上性心动过速（PSVT）急性症状性发作的疗法，开拓了PSVT治疗新场景。患者可在无医疗监督的环境（如居家）自行给药，实现对病情的主动掌控，使疾病管理从依赖急诊干预转向更加主动的院外管理。此外，艾曲帕米鼻喷雾剂正开发用于伴有快速心室率反应的房颤（AFib-RVR）适应症，II期临床研究已取得积极结果，并计划推进III期临床研究，未来有望进一步拓展至更广泛患者人群。在中国，艾曲帕米鼻喷雾剂用于治疗PSVT的新药上市申请已于2025年1月17日获中国国家药品监督管理局（NMPA）正式受理，并预计于2026年第三季度获批，有望为PSVT患者提供全新的治疗选择。PSVT是一种以突发突止为主要特征的心动过速临床综合征，发作时心率极快且节律规则，通常持续数分钟至数小时，患者症状明显且恐惧感强。PSVT急性发作的治疗缺乏安全、便捷、可在院外自行使用的快速终止药物，使患者在发作期长期处于"被动等待"状态，缺乏真正意义上的"按需自救"工具。据悉，在中国，每1000中约有2.3-4人患有PSVT，估计总患者人数为300-600万。AFib-RVR的特征是心率不规则，紊乱且快速，呈渐进式发作且不易自行终止，容易反复持续。目前中国的房颤患病率1.6%，对应患者人数约2000万，并随老龄化加剧呈上升趋势。PSVT与AFib-RVR都会增加患者的失控感和心理负担。整体来看，PSVT及AFib-RVR患者人群规模超过2500万人，临床需求远未得到满足，亟需更便捷、更高效的治疗选择。临床数据方面，此次艾曲帕米鼻喷雾剂获中国NMPA新药上市申请受理是基于艾曲帕米关键性III期 RAPID 研究和中国III期 JX02002 临床研究所取得的数据结果。JX02002研究达到了方案预设的主要终点，治疗期出现的不良事件（TEAEs）在艾曲帕米治疗组和安慰剂组之间相当。艾曲帕米鼻喷雾剂获FDA批准是基于一项扎实的临床试验项目所得出的结论，该项目共收集了来自超1,800名参与者、超2,000次PSVT发作的安全性数据。这包括成功的3期RAPID试验，这是一项在全球范围内开展的、随机、双盲、安慰剂对照研究，结果于2023年发表在《柳叶刀》杂志上。RAPID试验达到了其主要终点：自行使用艾曲帕米的参与者（N=99）中有64%在30分钟内从室上性心动过速转为窦性心律，而安慰剂组（N=85）为31%（HR = 2.62; p