SHENZHEN, Feb 24, 2026 - (ACN Newswire via SeaPRwire.com) - China Medical System Holdings Limited (“CMS” or the “Group”) is pleased to announce that its subsidiary, Dermavon Holdings Limited (“Dermavon”, an innovative pharmaceutical company specialized in skin health which is applying for a separate listing on the Main Board of The Stock Exchange of Hong Kong Limited, please refer to the announcement published by the Group on 22 April 2025 for details) received the acceptance from the National Medical Products Administration of China (NMPA) for the New Drug Application (NDA) of ruxolitinib phosphate cream (the “Product”) for the treatment of mild to moderate atopic dermatitis on 24 February 2026. The Product is indicated for the topical short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in non-immunocompromised adult and pediatric patients 2 years of age and older whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. The NDA has been approved for inclusion in the Priority Review List by the Center for Drug Evaluation (CDE) of the NMPA based on its qualification as a “new variety, dosage form and specification of pediatric drug that conforms to the physiological characteristics of children”, which is expected to accelerate the Product's review process for marketing approval in the AD indication.Impressive phase III trial data in ADIts Priority Review is expected to accelerate its NDA approvalRuxolitinib phosphate cream was approved for marketing by the NMPA in January 2026, becoming the first and only targeted drug approved in China for the treatment of vitiligo. The acceptance of this NDA for the additional indication of AD marks a key milestone in the Product's expansion into multiple therapeutic areas.Ruxolitinib phosphate cream has achieved positive results in a randomized, double-blind, placebo-controlled Phase III clinical trial in China for mild to moderate AD.Robust Efficacy: The Product successfully met its primary endpoint, demonstrating that a significantly higher proportion of subjects treated with ruxolitinib phosphate cream achieved IGA (Investigator’s Global Assessment) of 0 or 1 with at least two grades of reduction from baseline at week 8, compared with placebo (63.0% vs 9.2%, P < 0.001). For the key secondary endpoint, the proportion of subjects achieving at least a 75% improvement from baseline in the Eczema Area and Severity Index score (EASI 75) of treatment with ruxolitinib phosphate cream was also significantly higher than that of the placebo group, at week 8 (78.0% vs 15.4%, P < 0.001).Favorable Safety Profile: The severity of treatment-emergent adverse events (TEAE) during the treatment period was mostly mild or moderate, with no TEAEs leading to discontinuation of the study drug. Overall, ruxolitinib phosphate cream was safe and well-tolerated.Furthermore, the NDA has been approved for inclusion in the Priority Review List. According to relevant NMPA regulations, the review timeline for marketing applications subject to Priority Review and Approval Procedure is substantially shortened—from the standard 200 days to 130 days. This significant reduction in the review timeline is expected to accelerate the marketing process of ruxolitinib phosphate cream for the AD indication, benefiting a wide range of patients at an earlier date.Building an integrated AD solution,strengthening Dermavon’s leadership in dermatologyAD is a chronic, recurrent and inflammatory dermatologic disease, with the main clinical manifestations of dry skin, chronic eczema-like lesions and obvious itching or pruritus, which may seriously affect the quality of life of patients. It is estimated that there were over 54 million AD patients in China as of 2024. Based on SCORAD scores, mild to moderate AD accounts for 98% of these cases, representing over 52.5 million patients[1]. Topical drugs are the most basic treatment for AD. Traditional topical medications such as topical corticosteroids (TCS) and topical calcineurin inhibitors (TCIs) have clinical pain points with long-term adverse reactions or limited efficacy, therefore novel treatments are urgently needed.Dermavon has developed a comprehensive “treatment + care” integrated solution for AD. In addition to the topical formulation ruxolitinib phosphate cream for mild-to-moderate AD, the portfolio also includes the injectable biological agent Comekibart Injection (MG-K10) for moderate-to-severe AD, the oral small molecule targeted drug CMS-D001 for moderate-to-severe AD, and the Heling Soothing Product Series for daily repair, to meet the management needs of AD patients from treatment to daily care.Simultaneously, the acceptance of the NDA for the AD indication will strengthen Dermavon’s strategic layout in the field of skin treatments and create synergies with its commercialized innovative drug ILUMETRI (tildrakizumab injection), commercialized exclusive drug Hirudoid (mucopolysaccharide polysulfate cream), and a series of innovative drugs under development and dermatological skin care products, in terms of expert network and market resources, thereby potentially enhancing Dermavon's market competitiveness and brand influence in the field of skin health.More Information About Ruxolitinib Phosphate CreamRuxolitinib phosphate cream (Opzelura®), a novel cream formulation of the selective JAK1/JAK2 inhibitor ruxolitinib developed by Incyte. In China, ruxolitinib phosphate cream is approved for the treatment of non-segmental vitiligo with facial involvement in children aged 12 years and older and adult patients. In the U.S., ruxolitinib phosphate cream is the first topical JAK inhibitor approved by the U.S. Food and Drug Administration (FDA) for the topical treatment of non-segmental vitiligo in patients aged 12 years and older, and for the topical short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in non-immunocompromised adult and pediatric patients 2 years of age and older whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable[2]. In Europe, ruxolitinib phosphate cream is approved for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age[3].The Group, through its subsidiary of Dermavon entered into a Collaboration and License Agreement with Incyte for ruxolitinib phosphate cream on 2 December 2022, obtaining an exclusive license to develop, register and commercialize the Product in Mainland China, Hong Kong Special Administrative Region, Macau Special Administrative Region, Taiwan Region and eleven Southeast Asian countries (the “Territory”) and a non-exclusive license to manufacture the Product in the Territory. The subsidiary of Dermavon has sublicensed the relevant rights for the Product outside of Mainland China to the Group (excluding Dermavon and its subsidiary).Incyte has worldwide rights for the development and commercialization of ruxolitinib phosphate cream, marketed in the United States and Europe as Opzelura®. Opzelura® and the Opzelura® logo are registered trademarks of Incyte.About CMSCMS is a platform company linking pharmaceutical innovation and commercialization with strong product lifecycle management capability, dedicated to providing competitive products and services to meet unmet medical needs.CMS focuses on the global first-in-class (FIC) and best-in-class (BIC) innovative products, and efficiently promotes the clinical research, development and commercialization of innovative products, enabling the continuous transformation of scientific research into clinical practices to benefit patients.CMS deeply engages in several specialty therapeutic fields, and has developed proven commercialization capabilities, extensive networks and expert resources, resulting in leading academic and market positions for its major marketed products. CMS continues to promote the in-depth development in its advantageous specialty fields, strengthening the competitiveness of the cardio-cerebrovascular/ gastroenterology/ ophthalmology/ skin health businesses, bringing economies of scale in specialty fields. Among them, the skin health business (Dermavon) has become a leading enterprise in its field, and is proposed to be listed independently on the SEHK. Meanwhile, CMS continuously promotes the operation and development of its integrated R&D, manufacturing and commercialization chain in Southeast Asia and the Middle East, capturing growth opportunities in emerging markets to support the high-quality and sustainable development of the Group.Reference:1. China Insights Consultancy’s industrial report2. The U.S. FDA approval information can be found on the Incyte official website, as follows:https://investor.incyte.com/news-releases/news-release-details/incyte-announces-additional-fda-approval-opzelurar-ruxolitinib3. The EMA approval information can be found on the Incyte official website, as follows:https://investor.incyte.com/news-releases/news-release-details/incyte-announces-european-commission-approval-opzelurarCMS Disclaimer and Forward-Looking StatementsThis press release is not intended to promote any products to you and is not for advertising purposes. This press release does not recommend any drugs, medical devices and/or indications. If you want to know more about the diagnosis and treatment of specific diseases, please follow the opinions or guidance of your doctor or other medical and health professionals. Any treatment-related decisions made by healthcare professionals should be based on the patient’s specific circumstances and in accordance with the drug package insert.This press release which has been prepared by CMS does not constitute any offer or invitation to purchase or subscribe for any securities, and shall not form the basis for or be relied on in connection with any contract or binding commitment whatsoever. This press release has been prepared by CMS based on information and data which it considers reliable, but CMS makes no representation or warranty, express or implied, whatsoever, and no reliance shall be placed on, the truth, accuracy, completeness, fairness and reasonableness of the contents of this press release. Certain matters discussed in this press release may contain statements regarding the Group’s market opportunity and business prospects that are individually and collectively forward-looking statements. Such forward-looking statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties and assumptions that are difficult to predict. Any forward-looking statements and projections made by third parties included in this press release are not adopted by the Group and the Company is not responsible for such third-party statements and projections.Media ContactBrand: China Medical System Holdings Ltd.Contact: CMS Investor RelationsEmail: ir@cms.net.cnWebsite: https://web.cms.net.cn/en/home/ Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

深圳, 2026年2月24日 - (亞太商訊 via SeaPRwire.com) - 康哲藥業控股有限公司 （「康哲藥業」）欣然宣佈，旗下德鎂醫藥有限公司（「德鎂醫藥」，專業聚焦皮膚健康的創新型醫藥企業，正申請於香港聯合交易所有限公司主板獨立上市，詳見康哲藥業日期為2025年4月22日發佈的公告）已於2026年2月24日獲得中國國家藥品監督管理局（NMPA）受理磷酸蘆可替尼乳膏（「產品」）輕中度特應性皮炎（「AD」）的新藥上市許可申請（NDA）。產品擬用於其他外用藥控制不佳或不建議使用時，非免疫功能受損的2歲及以上兒童和成人輕中度特應性皮炎的局部短期和非持續性慢性治療。且該項NDA因「符合兒童生理特徵的兒童用藥品新品種、劑型和規格」，已獲得NMPA藥品審評中心批准納入優先審評品種名單，有望加快產品AD適應症上市審評進程。特應性皮炎III期臨床數據亮眼，優先審評加速上市磷酸蘆可替尼乳膏已於2026年1月獲得NMPA批准上市，成爲中國批准的首款且唯一用於白癜風治療的靶向藥。此次增加AD適應症NDA獲受理，是產品向多治療領域拓展的關鍵里程碑。磷酸蘆可替尼乳膏已在輕中度AD的一項隨機、雙盲、安慰劑對照中國三期藥物臨床研究取得積極結果：- 療效優異：產品成功達到主要終點，即使用產品治療8周，達到研究者整體評估（IGA）評分為0或1分，且較基線改善≥2分的受試者比例，顯著高於安慰劑（63.0% vs 9.2%，P<0.001）。關鍵次要終點，磷酸蘆可替尼乳膏治療8周，達到濕疹面積及嚴重程度指數評分較基線至少改善75%（EASI 75）的受試者比例亦顯著優於安慰劑（78.0% vs 15.4%，P<0.001）。- 安全性良好：治療期出現的不良事件（TEAE）的嚴重程度大多數為輕度或中度，未發生導致研究藥物用藥終止的TEAE，整體安全耐受性良好。此外，該項NDA已獲批納入優先審評品種名單。根據NMPA相關規定，適用優先審評審批程序的上市註冊申請的審評時限由常規程序的200日大幅縮短爲130日，審評時限將得到顯著縮短，這將有望加速磷酸蘆可替尼乳膏AD適應症的上市進程，早日惠及廣大患者。構建特應性皮炎綜合方案，強化皮膚領域競爭實力AD是一種慢性、復發性、炎症性的皮膚疾病，臨床主要表現為皮膚乾燥、慢性濕疹樣皮損和明顯瘙癢，可能嚴重影響患者的生活品質。據估算，2024年中國特應性皮炎患者超過5,400萬人，基於SCORAD評分，輕中度特應性皮炎的占比為98%，即超過5,250萬患者[1]。外用藥物是AD最基本的治療方法。傳統外用藥物如外用糖皮質激素（TCS）及外用鈣調神經磷酸酶抑制劑（TCIs）有長期用藥的不良反應或療效有限的臨床痛點，臨床亟需新的治療選擇。德鎂醫藥已針對AD構建了全方位的「治療+護理」綜合解決方案，除局部外用製劑-磷酸蘆可替尼乳膏（輕中度AD）外，還包括注射用生物製劑-柯美奇拜單抗注射液-MG-K10（中重度AD）、口服小分子靶向藥-CMS-D001（中重度AD）、日常修護-禾零舒緩產品系列，滿足AD患者從治療到日常護理的管理需求。同時，此次增加AD適應症NDA獲受理，將進一步強化德鎂醫藥在皮膚治療領域的戰略佈局，並與現有處於商業化階段的創新藥益路取（替瑞奇珠單抗注射液）、獨家藥喜遼妥（多磺酸粘多糖乳膏），以及系列在研創新藥和皮膚學級護膚品等在專家網絡與市場資源等方面產生協同，提升德鎂醫藥在皮膚健康領域的市場競爭力與品牌影響力。關於磷酸蘆可替尼乳膏的更多信息磷酸蘆可替尼乳膏（Opzelura(R)）是Incyte開發的選擇性JAK1/JAK2抑制劑蘆可替尼製成的一種創新型乳膏。在中國，磷酸蘆可替尼乳膏獲批用於治療12歲及以上兒童和成人患者伴面部受累的非節段型白癜風。在美國，磷酸蘆可替尼乳膏是經美國食品和藥物管理局（FDA）批准的首款局部JAK抑制剂，可用於局部治療12歲及以上患者的非節段型白癜風；及其他外用藥控制不佳或不建議使用時，非免疫功能受損的2歲及以上兒童和成人輕中度特應性皮炎的局部短期和非連續性慢性治療[2]。在歐洲，磷酸蘆可替尼乳膏被批准用於治療成年及12歲及以上青少年面部受累的非節段型白癜風[3]。康哲藥業於2022年12月2日，通過德鎂醫藥的附屬公司與Incyte就磷酸蘆可替尼乳膏訂立合作和許可協議（「許可協議」），獲得在中國大陸、香港特別行政區、澳門特別行政區、臺灣地區及東南亞十一囯（「區域」）研發、注冊及商業化產品的獨家許可權利，以及在區域內生產產品的非獨家許可權利。德鎂醫藥的附屬公司已將磷酸蘆可替尼乳膏除中國大陸外的其他區域的相關權利再許可予康哲藥業（不包括德鎂醫藥及其附屬公司）。Incyte擁有磷酸蘆可替尼乳膏全球開發和商業化權利，在美國及歐洲以Opzelura(R)的名稱銷售。Opzelura(R)和Opzelura(R)標識是Incyte的註冊商標。關於康哲藥業康哲藥業是一家鏈接醫藥創新與商業化，把控產品全生命週期管理的開放式平臺型企業，致力於提供有競爭力的產品和服務，滿足尚未滿足的醫療需求。康哲藥業專注於全球首創（FIC）及同類最優（BIC）的創新產品，並高效推進創新產品臨床研究開發和商業化進程，賦能科研成果向診療實踐的持續轉化，造福患者。康哲藥業聚焦專科領域，擁有被驗證的商業化能力，廣泛的渠道覆蓋和多疾病領域專家資源，核心在售產品已獲領先的學術與市場地位。康哲藥業圍繞優勢專科領域不斷縱深發展，以鞏固心腦血管/消化/眼科/皮膚健康業務競爭力，帶來專科規模效率，其中皮膚健康業務（德鎂醫藥）已成為其細分領域的龍頭企業，並擬於聯交所獨立上市。同時，康哲藥業持續推動研產銷全產業鏈在東南亞及中東區域運營發展，以獲取新興市場的增量，助力集團實現高質量可持續發展。參考文獻/資料1.數據來自灼識諮詢報告2.FDA批准信息可在Incyte官網查詢，網址：https://investor.incyte.com/news-releases/news-release-details/incyte-announces-additional-fda-approval-opzelurar-ruxolitinib3.EMA批准信息可在Incyte官網查詢，網址：https://investor.incyte.com/news-releases/news-release-details/incyte-announces-european-commission-approval-opzelurar康哲藥業免責與前瞻性聲明本新聞無意向您做任何產品的推廣，非廣告用途。本新聞不對任何藥品和-醫療器械和/或適應症作推薦。若您想瞭解具體疾病診療資訊，請遵從醫生或其他醫療衛生專業人士的意見或指導。醫療衛生專業人士作出的任何與治療有關的決定應根據患者的具體情況並遵照藥品說明書。由康哲藥業編制的此新聞不構成購買或認購任何證券的任何要約或邀請，不形成任何合約或任何其他約束性承諾的依據或加以依賴。本新聞由康哲藥業根據其認為可靠之資料及數據編制，但康哲藥業並無進行任何說明或保證、明述或暗示，或其他表述，對本新聞內容的真實性、準確性、完整性、公平性及合理性不應加以依賴。本新聞中討論的若干事宜可能包含涉及康哲藥業的市場機會及業務前景的陳述，該等陳述分別或統稱為前瞻性聲明。該等前瞻性聲明並非對未來表現的保證，存在已知及未知的風險、不明朗性及難以預知的假設。康哲藥業並不採納本新聞包含的第三方所做的任何前瞻性聲明及預測，康哲藥業對該等第三方聲明及預測不承擔責任。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亞太商訊 via SeaPRwire.com) - 康希諾生物（688185.SH/06185.HK）宣佈，公司自主研發的ACYW135群腦膜炎球菌多糖結合疫苗（CRM197載體）——曼海欣(R)擴大適用人群的補充申請已正式獲得國家藥品監督管理局批准。此次獲批後，曼海欣(R)適用於3月齡至6周歲（83月齡）的嬰幼兒及兒童，用於預防由A、C、Y、W135群腦膜炎奈瑟菌引起的流行性腦脊髓膜炎（以下簡稱"流腦"）。此次曼海欣(R)擴齡獲批，具有重要的公共衛生和商業發展意義。一方面，在我國現行免疫規劃程式中，6歲是入學前流腦疫苗接種"最後一針"的重要節點，長期以來，國內針對3歲以上兒童的多價流腦結合疫苗選擇相對有限。曼海欣(R)此次擴齡獲批，為學齡期兒童提供了四價流腦多糖結合疫苗接種選擇，有助於填補兒童流腦防控在關鍵年齡階段的保護空白，進一步完善我國流腦免疫屏障。另一方面，適用人群範圍的擴大，將有助於曼海欣(R)進一步釋放產品潛力，提升商業化空間，並為該產品在國際市場的推廣與佈局奠定更為堅實的基礎。值得一提的是，康希諾生物日前已發佈2025年度業績預告，全年營收預計10.4–10.8億元，同比增長22.88%-27.61%；歸母淨利潤預計2450萬–2900萬元，將實現扭虧為盈。同時，公告明確指出，"公司持續踐行以創新為核心、以商業化落地為重點的發展戰略，中國首款四價流腦結合疫苗曼海欣(R)收入保持持續增長"。這也意味著康希諾生物已進入創新疫苗商業化收穫期。依託獨家技術平台、領先優勢及加速的國際化佈局，曼海欣(R)擴齡不僅鞏固了市場競爭力，也為康希諾生物的可持續增長注入新的動力。隨著產品覆蓋和國際拓展的推進，公司長期價值將開啟更廣闊的發展空間。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亞太商訊 via SeaPRwire.com) - 2026年2月22日, 納斯達克上市公司迦里仕人才集團有限公司（Galaxy Payroll Group Limited，NASDAQ: GLXG，以下簡稱「迦里仕人才」）今日宣布，已與耐吉中國控股香港有限公司澳門分公司（NIKE China Holding HK Limited (Macau Branch)，以下簡稱「耐吉澳門分公司」）正式續簽為期五年的戰略合作協議。合作再延五年，服務範圍全面覆蓋核心HR職能根據協議，雙方合作期限自2025年12月1日起至2030年11月30日止。在此期間，迦里仕人才將繼續為耐吉澳門分公司提供涵蓋本地薪資發放、考勤與休假管理、社保及稅務合規申報，以及勞動法規與用工政策咨詢在內的一站式人力資源外包服務。該合作模式有效支持耐吉澳門分公司聚焦其核心零售與品牌運營，提升整體組織效能。戰略續約彰顯客戶高度信任，強化收入穩定性此次續約不僅是雙方合作關系邁入新階段的重要標志，更體現了國際頭部品牌對迦里仕人才專業能力、合規水平及長期服務交付質量的高度認可。中長期合約的簽署顯著增強了公司未來五年收入的可預測性與現金流穩定性，進一步契合其打造高質量、抗周期業務模型的資本市場戰略。本地化能力構築核心壁壘，服務體系持續進化自2013年成立以來，迦里仕人才始終深耕港澳市場，並逐步拓展跨區域服務能力。公司憑借對香港及澳門勞動法、稅務及社保政策的深度掌握，建立起紮實的本地合規能力；同時依托標准化流程與定制化方案相結合的服務體系，確保交付的一致性與可擴展性。其自主開發的薪資與考勤管理平臺，在提升運營效率的同時有效保障數據安全與業務連續性，成為吸引並維系跨國企業客戶的關鍵優勢。在過往合作中，迦里仕人才已多次協助耐吉澳門分公司應對複雜用工環境下的合規挑戰，其解決方案在准確性、響應速度及風險控制方面均獲得充分驗證，為本次長期續約奠定了堅實基礎。展望未來：從服務交付邁向價值共創展望新合作周期，迦里仕人才將在現有服務框架基礎上，持續優化薪資管理流程與智能考勤系統，並通過數據整合與定期管理報表，助力客戶推進人力資源管理的規範化與數字化轉型。雙方亦約定保留通過補充協議靈活拓展服務範圍的機制，確保合作節奏與客戶業務發展動態同步。此次五年期戰略合作的續簽，不僅是對迦里仕人才專業價值的長期肯定，更是對其商業模式可持續性的有力印證。它將進一步鞏固公司在港澳及亞太人力資源外包市場的品牌影響力，並為服務更多跨國零售、體育及消費品牌提供可複制的標杆案例。在全球企業日益重視合規效率、成本優化與組織韌性的背景下，迦里仕人才正憑借其深厚的本地化經驗、穩健的服務體系與高粘性的優質客戶基礎，穩步構建長期增長動能。公司管理層表示：「我們將繼續以服務能力為核心驅動力，深化與現有優質客戶的戰略合作，同時積極拓展更多具有長期價值的跨國及區域性企業客戶，持續為股東創造穩健、可持續的回報。」 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亞太商訊 via SeaPRwire.com) – 2026年新版《道路機動車輛生產企業准入審查要求》中，仿真驗證能力被作為強制性關鍵要素寫入准入審查要求，國產仿真平臺迎來巨大的市場利好，進一步推動了智駕產業鏈加速向「自主可控」邁進。在此背景下，五一視界宣布旗下51Sim下一代智駕仿真平臺 SimOne 4.0 已於近日成功完成在摩爾線程旗艦級AI訓推一體全功能GPU MTT S5000上的系統性適配與深度優化。從大模型感知挖掘、4DGS模型訓練到4DGS仿真推理和合成數據生成，雙方強強聯手，實現了國產算力與端到端智能駕駛仿真體系的完整打通，正式開啟了物理AI智駕領域高置信度閉環仿真與合成數據的全棧國產化新篇章,為應對新規下的嚴苛驗證需求提供了堅實的國產底座。算力底座的「跨代式」追趕隨著端到端智駕收斂到VLA和世界模型兩條路線，基於海量Log數據的高置信度閉環仿真和合成數據已成為提升算法長尾場景處理能力的關鍵命題。仿真效率的上限，往往取決於基礎一硬件的規格。在很長一段時間裏，高端GPU市場幾乎被海外巨頭壟斷，但五一視界與摩爾線程的最新合作成果顯示，這一格局正在發生微妙的變化。SimOne 4.0已完成與摩爾線程MTT S5000的深度適配。MTT S5000是專為大模型訓練、推理及高性能計算而設計的全功能GPU智算卡，基於第四代MUSA架構「平湖」打造。其單卡AI算力（稠密）最高可達1000 TFLOPS，配備80GB顯存，顯存帶寬達到1.6TB/s，卡間互聯帶寬為784GB/s，完整支持從FP8到FP64的全精度計算。基於SimOne 4.0實現7個周視攝像頭4DGS場景重建效果在實測數據中，MTT S5000展現出了足以抗衡甚至部分超越國際主流競品的硬實力。數據顯示，MTT S5000在FP32、FP16及INT8等關鍵精度上實現了約1.47倍的性能增長，FP64雙精度算力領先幅度約1.48倍。更值得關注的是其搭載的MTLink技術，使得卡間帶寬提升約30%。MTT S5000憑借FP8提升訓推效率、FP64保障計算精准、光線追蹤實現高保真渲染，以自主可控的強勁底層算力，為智能駕駛提供安全、高效、可靠的核心國產算力支撐。場景實測：在複雜博弈中驗證「真功夫」硬件參數的領先，最終需要在真實的算法場景中落地。在SimOne 4.0的大模型感知挖掘功能中，雙方針對Qwen3-VL多模態大模型進行了深度調優。實測結果令人驚喜：無論是在8B模型還是更複雜的30B MoE架構下，MTT S5000在「預填充（Prefill）」階段的首字響應速度（TTFT）均優於國際主流競品，優勢最高擴大至14%，且在10並發的高壓環境下依然保持了穩健的吞吐量。而在更考驗訓練和推理能力的4DGS（4D高斯潑濺）領域，基於51Sim入選AAAI 2026的LidarPainter技術，國產算力同樣經受住了考驗。目前測試數據顯示，在訓練端，MTT S5000展現出比肩國際主流競品的強勁性能，僅需2.5小時即可完成一個真實Clip場景的高質量重建；在推理端，面對單Clip包含1600萬個高斯點的超大模型負載，MTT S5000成功實現了11路攝像頭加1路激光雷達的實時閉環仿真，呈現出像素級的高保真效果。這證明了國產顯卡在處理複雜光影與動態物體還原時，已經具備了生產力級別的屬性,能夠勝任准入審查中要求的極端工況與邊界條件驗證。這種高保真物理場景的重建能力，同樣可遷移至具身智能機器人的空間感知與操作訓練中。基於LidarPainter 技術生成高真實度新視角圖像隱形護城河：構建「芯片+系統」的通用底座如果說高性能GPU的適配是攻克了「最難的骨頭」，那麼對國產基礎軟硬件生態的全面覆蓋，則是五一視界構築的一條安全護城河,也是響應國家信創戰略、滿足敏感行業准入要求的關鍵。除了圖形計算領域，五一視界已悄然完成了對主流國產芯片架構的全線互認。在CPU層面，無論是基於ARM架構的華為鯤鵬、飛騰，還是基於x86架構的海光、兆芯，五一視界旗下的51Aes、51Sim等核心產品均已實現流暢部署。特別是通過華為鯤鵬技術認證並加入「鯤鵬展翅」計劃，進一步夯實了其在國產服務器端的運行穩定性。在操作系統層面，為了徹底擺脫對非國產發行版的依賴，五一視界將適配工作下沉至系統內核，先後完成了與麒麟軟件（銀河麒麟高級服務器操作系統）及統信軟件（UOS）的適配認證。這一舉措意味著，對於政府、能源等有著嚴苛信創要求的敏感行業客戶而言，他們可以選擇從芯片到底層操作系統到上層應用全鏈路自主可控的數字孿生解決方案,從容應對日益嚴格的合規性審查,構建起一個不僅服務於智能駕駛，更能廣泛賦能於人形機器人等具身智能終端的國產化通用基礎設施。中國科技企業「國產自主可控」已經崛起從攜手摩爾線程在高端算力上撕開缺口，到打通華為鯤鵬、麒麟等操作系統的生態脈絡，再到積極響應新版准入審查要求提供合規的仿真驗證能力，五一視界的這一系列動作表明，中國企業的「國產自主可控」正在發生量變和質變，正在緩緩崛起。這不再是簡單的參數對標，而是產業生態的戰略閉環。SimOne 4.0的表現證明，國產軟硬件方案已經邁過了「能用」的門檻，正式進入了高精度、高負載任務的「好用」階段。隨著算法與算力的深度融合，以及政策法規對仿真驗證能力的強制加持，一個繁榮的、自主可控的物理AI生態底座正在逐步成型，為中國智能駕駛產業的獨立發展保駕護航,也為具身智能機器人等新興領域的國產化落地鋪平了道路。基於SimOne 4.0 的4DGS閉環仿真 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亞太商訊 via SeaPRwire.com)  – 2月23日，由上海實業（集團）有限公司（以下簡稱「上實集團」）與國泰海通證券股份有限公司（以下簡稱「國泰海通」）聯合發起設立的滬港新興產業基石基金（以下簡稱「基石基金」）正式啟航，進入實質投資階段。作為全國首支、上海市級市場化運作的證券類港股基石基金，基金目標總規模30億港元，首期規模10億港元，將聚焦集成電路、生物醫藥、人工智能上海三大先導產業，專項支援優質企業赴港上市，深化滬港金融與產業協同。服務上海戰略，強化滬港聯動上海市政府和上海市國資委指導設立的基石基金，是上海國資服務上海科技創新中心建設、推動重點產業高質量發展的重要舉措，將緊密圍繞上海前瞻的集成電路、生物醫藥、人工智能三大先導產業進行戰略佈局，通過資本市場賦能，加速本地創新企業國際化進程。同時，基金也將充分發揮香港作為國際金融中心的樞紐功能，構建「上海產業+香港資本」的高效聯通機制，促進兩地金融資源互補與市場互聯，打造滬港合作新標杆。創新「雙管理人」架構，滙聚兩地專業力量基石基金在治理模式上採用創新的「雙管理人」架構，由上實集團在港金融投資業務平台上實資本（香港）投資管理有限公司，和國泰海通在港資產管理平台海通國際資產管理有限公司共同擔任基金管理人，並由滬港兩地協同運營。這一合作架構充分融合了上實集團作為上海在港窗口企業的產業資源與香港本地的運營優勢，及國泰海通在全球資本市場和跨境資產管理方面的專業能力，實現「產業+金融」、「上海+香港」的雙重優勢互補。通過建立完善的投資決策機制與風險控制體系，該架構既確保了基金運作符合國際標準，又保持了與本土產業生態的深度連結，為基金的長期穩健運作奠定了堅實基礎。多元化投資策略，專注長期價值基石基金堅持市場化、專業化、國際化運作原則，以產業、金融雙重視角，構建覆蓋企業全生命週期的投資與賦能體系。通過靈活的多元化策略組合與深度投後服務，系統性支援上海三大先導產業優質企業的業務發展與價值實現。基石基金在重點參與上海三大先導產業優質企業赴港IPO的基石投資之外，還可以參與港股IPO錨定和已上市港股的配售投資，通過無鎖定期策略保持基金的流動性，以保證基金投資收益；在市場大幅下跌時，也可通過二級市場方式，增持價值低估的優質公司股票；同時跟進優秀企業再融資及併購重組，助力可持續發展。基石基金將嚴格遵循「好賽道、好公司、好價格」的遴選標準，重點投向具備核心技術、高成長性和穩健現金流的行業領軍企業。強化上海國資在港功能，構建跨境投資新平台基石基金是上實集團和國泰海通強化在港服務功能、完善跨境投資佈局的關鍵舉措之一。基石基金不僅進一步完善上海國資基金矩陣，填補國資基金在港股IPO及二級市場策略的空白，服務上海企業赴港上市「最後一公里」融資需求，助力構建「早期投資—成長期融資—公開市場上市」的完整產業投資生態；更通過上實集團和國泰海通的深度合作，強強聯手、協作共贏，系統提升跨境合規、資產配置與複雜交易設計能力，進一步增強上海國資服務上海乃至國家戰略的綜合實力。展望：鏈接國際資本，賦能創新未來在全球科技創新競爭日益激烈的背景下，滬港新興產業基石基金的實質啟動，標誌著上海在對接國際資本市場、服務本土創新方面邁出系統性的一步。在人民幣國際化和「惠港五條」等政策紅利支持下，基石基金將成為連接內地產業資本與國際金融資源的重要紐帶。未來，基石基金將積極把握人民幣國際化與金融市場雙向開放機遇，持續促進國際資本投資上海核心產業，為上海三大先導產業企業提供全方位的資本服務，助力更多硬科技企業走向世界，為滬港融合與高質量發展貢獻力量。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

SAN DIEGO, Feb 23, 2026 - (ACN Newswire via SeaPRwire.com) - General Atomics Aeronautical Systems, Inc. (GA-ASI) is giving its U.S. Air Force Collaborative Combat Aircraft a new name: YFQ-42A Dark Merlin.Dark merlins, deadly falcons known for their black feathers and devouring of other falcons as prey, often collaborate in groups for maximum effect against their targets. The Cornell Lab of Ornithology describes the merlin as a "small, fierce falcon that uses surprise attacks" to bring down its prey in flight. The dark merlin is native to the Pacific Northwest of the United States, often migrating into southern California, where bird spotters routinely report seeing them near the YFQ-42A's manufacturing home in San Diego.The 1962 book "Profiles of the Future" imagined global technological marvels yet to change the world, offering that "any sufficiently advanced technology is indistinguishable from magic." It's no coincidence that the Dark Merlin name also reflects the wizardry of Merlin from Arthurian legend, paying homage to the somewhat supernatural new era of semi-autonomous air combat."Dark merlins are hunting machines, built for speed and aerodynamics," said GA-ASI President David R. Alexander. "They harass other falcons for fun, and they eat what they kill. The name sums up our new uncrewed fighter perfectly."The U.S. Air Force official prefix "Y" denotes that the initial few aircraft are early, production-representative test models, while "F" denotes fighter and "Q" denotes uncrewed aircraft. When aircraft enter production, they drop the "Y" - for example, the YF-16 became the F-16 with the nickname "Fighting Falcon" - and GA-ASI expects its new CCA to become the FQ-42A with the nickname "Dark Merlin."The Dark Merlin has been stacking up milestones and achievements since GA-ASI was selected by the U.S. Air Force in April 2024 to build production-representative flight test articles for the CCA program. In August 2025, YFQ-42A delivered the U.S. Air Force its first successful CCA flight and followed that this month with the service's first CCA flight using mission autonomy software. Between those milestones, GA-ASI has built and flown multiple Dark Merlins, conducting push-button autonomous takeoffs and landings and other accomplishments as the test program continues.YFQ-42A Dark Merlin is a purpose-built CCA platform developed as part of GA-ASI's ongoing investment in next-generation autonomous combat aircraft. The aircraft's modular design enables rapid integration of mission systems. GA-ASI's autonomy architecture, demonstrated through multiple live flight tests, provides the foundation for human-machine teaming in complex combat scenarios.GA-ASI has been building and flying uncrewed jets for nearly two decades, beginning with the company-funded, weaponized MQ-20 Avenger® in 2008. Ongoing company investment in Avenger continues to yield results, as the aircraft routinely serves as a CCA surrogate for advanced autonomy development and testing in both government programs and company-funded research and development. The company's XQ-67A Off-Board Sensing Station jet, developed in collaboration with the U.S. Air Force Research Laboratory, offers a cutting-edge model for autonomous collaborative platforms with advanced airborne sensing and served as a flying prototype for YFQ-42A Dark Merlin.About GA-ASIGeneral Atomics Aeronautical Systems, Inc., is the world's foremost builder of Unmanned Aircraft Systems (UAS). Logging more than 9 million flight hours, the Predator® line of UAS has flown for over 30 years and includes MQ-9A Reaper®, MQ-1C Gray Eagle®, MQ-20 Avenger®, and MQ-9B SkyGuardian®/SeaGuardian®. The company is dedicated to providing long-endurance, multi-mission solutions that deliver persistent situational awareness and rapid strike.For more information, visit www.ga-asi.com.Avenger, EagleEye, Gray Eagle, Lynx, Predator, Reaper, SeaGuardian, and SkyGuardian are trademarks of General Atomics Aeronautical Systems, Inc., registered in the United States and/or other countries.GA-ASI Media RelationsGeneral Atomics Aeronautical Systems, Inc.ASI-MediaRelations@ga-asi.com(858) 524-8101SOURCE: General Atomics Aeronautical Systems, Inc. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

HONG KONG, Feb 23, 2026 - (ACN Newswire via SeaPRwire.com) – During the Year of the Horse Spring Festival, momentum in the "Hard Tech" sector continued to surge, with the humanoid robotics industry becoming a market focal point following its stellar performance on the Spring Festival Gala stage. Shoucheng Holdings (0697.HK) has emerged as a core target for post-holiday capital market positioning due to a series of heavy-hitting moves. These include the operational launch of the Taozhu New Creation Hub - a comprehensive robotics technology experience, sales, maintenance, and service center—followed by the dual boost of Spring Festival Gala exposure and New Year's Eve livestreaming conversions. Coupled with the positive signal of continuous recent share buybacks, the company’s solid industrial layout and clear earnings growth are expected to trigger a formal valuation recovery.By establishing a closed-loop of "Offline Landing + Strategic Investment + Traffic Conversion + Buyback Support," Shoucheng Holdings has not only demonstrated its deep layout in the robotics track but has also provided the capital market with a high-certainty investment logic through concrete industrial actions and capital behavior. The window for valuation recovery has officially opened.I. Grand Opening of the Offline Complex: Solidifying the Foundation for MonetizationAs the traffic dividends from the Spring Festival Gala and livestreaming were released, Shoucheng Holdings officially launched Taozhu New Creation Hub, its flagship robotics technology retail brand. This complex captures the core of the offline smart consumption track and injects deterministic growth into Shoucheng’s performance. It serves as a solid physical carrier to convert gala traffic and livestreaming orders, marking a new stage in Shoucheng’s full-chain service layout for offline robotics commercial scenarios.Integrated Ecosystem: The Hub constructs an "Experience + Sales + After-sales + Investment" full-model ecosystem."Store-Factory" Innovation: Utilizing an innovative "front-store, back-factory" layout, it includes a robotics maintenance and repair workshop created in collaboration with Accelerated Evolution to provide one-stop services.Market Validation: With an exhibition area exceeding 400 square meters, the Hub serves as a core scenario for investee companies to implement technology and validate market demand.Strategic Store Matrix:Wangfujing APM Store: Located in a premier trendy commercial district, focusing on "Trend Tech + First-Store Economy," targeting consumers aged 18–35.Capital Airport T2 Store: Situated in a core transportation hub with 35 million annual passengers, targeting the "40-minute pre-boarding decision" window with portable and practical smart products.This layout is a key execution of Shoucheng’s "Capital + Scenario + Ecosystem" strategy. By capturing consumer demand through digital means, it provides investee companies with valuable data for product iteration, forming a virtuous cycle of "Industry + Consumption + Maintenance".II. Dominance of the Gala Trio: National-Level Endorsement of Ecosystem StrengthThe Year of the Horse Spring Festival Gala featured a humanoid robot cluster performance as its most high-tech highlight. Among the four core robotics companies featured, three - Unitree Robotics, NOETIX Robotics, and Galbot - are Shoucheng Holdings' portfolio companies. This dominant presence provides national-level brand endorsement for the offline scenarios.The three portfolio companies demonstrated world-class capabilities across core tracks:Unitree Robotics: Deployed a 16-robot formation in the program "Wu BOT," performing high-difficulty martial arts. It achieved world-firsts in continuous parkour flips and rapid maneuvers (up to 4m/s) using self-developed dexterous hands.NOETIX Robotics: Earned the title of "Exclusive Bionic Humanoid Robot Partner" for the gala. Its "Xiaowantong N2" and "Xiaobumi" consumer products displayed lifelike facial expressions and synchronized breathing movements, signaling the acceleration of robots entering the home.Galbot: Debuted as the "Designated Embodied AI Model Robot". Its robot, "Xiao Gai," autonomously performed real-time tasks—such as picking up glass shards and folding clothes—driven by its "AstraBrain" Embodied AI model.This collective appearance is a result of Shoucheng's long-term deep layout, building a complete investment matrix across core components, whole units, and "intelligent brains".III. New Year's Eve Live-streaming: Immediate Traffic MonetizationOn the night of the Gala, Shoucheng Holdings launched the "PoBiren (Barrier-Breaker) Initiative" Live-streaming event, becoming the only industrial investor in the sector to achieve immediate traffic conversion. This successfully closed the loop of "Offline Landing - Stage Exposure - Online Traffic - Order Conversion".Solving Pain Points: The livestream addressed the "unreachable" nature of online consumption through product demonstrations and professional technical interpretations.Seamless Integration: It linked online orders to the Taozhu New Creation Hub for offline delivery and maintenance.Professional Branding: By sharing industry trends from an investor's perspective, Shoucheng deepened consumer trust and solidified its leadership in hard tech investment.ConclusionShoucheng Holdings has achieved a triple breakthrough in national exposure, immediate traffic conversion, and offline operations. Under the resonance of these multiple benefits and continued buybacks, the logic for both valuation and performance enhancement is further strengthened, allowing Shoucheng to lead the hard tech investment track and provide long-term stable returns to investors. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

HONG KONG, Feb 24, 2026 - (ACN Newswire via SeaPRwire.com) – February 22, Galaxy Payroll Group Limited (NASDAQ: GLXG) (“Galaxy” or the “Company”), a Nasdaq-listed human resources solutions provider, today announced that it has formally renewed a five-year strategic cooperation agreement with NIKE China Holding HK Limited (Macau Branch) (“Nike Macau Branch”).Five-Year Renewal with Comprehensive HR Service CoveragePursuant to the agreement, the renewed cooperation term will commence on December 1, 2025 and continue through November 30, 2030. During this period, Galaxy will continue to provide Nike Macau Branch with a comprehensive suite of human resources outsourcing services, including local payroll processing, attendance and leave management, social security and tax compliance filings, as well as advisory services relating to labor regulations and employment policies.This integrated service model is designed to enable Nike Macau Branch to focus on its core retail and brand operations while enhancing overall organizational efficiency and compliance management.Strategic Renewal Reflects Client Confidence and Enhances Revenue VisibilityThe renewal marks an important milestone in the long-standing relationship between the parties and reflects the continued trust placed in Galaxy’s professional capabilities, compliance standards, and service delivery quality by a leading international brand.The execution of a multi-year agreement is expected to enhance the Company’s revenue visibility and cash flow stability over the next five years, further aligning with its capital markets strategy of building a high-quality, resilient, and sustainable business model. While the agreement provides for long-term cooperation, actual results may vary and remain subject to market and operational conditions.Local Expertise and Scalable Service Infrastructure as Core Competitive AdvantagesSince its establishment in 2013, Galaxy has focused on the Hong Kong and Macau markets while progressively expanding its cross-regional service capabilities. The Company has developed deep expertise in Hong Kong and Macau labor laws, taxation, and social security regulations, forming a strong local compliance foundation.Through a service framework that combines standardized operational processes with customized solutions, Galaxy delivers consistency and scalability across its client base. Its proprietary payroll and attendance management platform enhances operational efficiency while supporting data security and business continuity, serving as a key differentiator in attracting and retaining multinational enterprise clients.Throughout prior phases of cooperation, Galaxy has supported Nike Macau Branch in navigating complex employment and compliance environments. The Company’s solutions have demonstrated reliability in accuracy, responsiveness, and risk control, providing a solid foundation for this long-term renewal.Looking Ahead: From Service Delivery to Value Co-CreationEntering the new cooperation cycle, Galaxy intends to further optimize payroll workflows and intelligent attendance systems within the existing service framework. Through enhanced data integration and periodic management reporting, the Company aims to support the client’s ongoing efforts toward standardized and digitalized human resource management.The parties have also agreed to retain flexibility to expand the scope of services through supplemental agreements, enabling the partnership to evolve in alignment with the client’s business development.The renewal of this five-year strategic agreement not only represents long-term recognition of Galaxy’s professional value, but also underscores the sustainability of its business model. It is expected to further strengthen the Company’s brand presence in the Hong Kong, Macau, and broader Asia-Pacific human resources outsourcing markets, while serving as a replicable benchmark case for multinational retail, sports, and consumer brands.As global enterprises increasingly prioritize compliance efficiency, cost optimization, and organizational resilience, Galaxy continues to leverage its localized expertise, robust service infrastructure, and high-quality client base to build sustainable long-term growth momentum.The Company’s management commented: “We will continue to place service capability at the core of our growth strategy, deepen strategic cooperation with existing high-quality clients, and proactively expand relationships with multinational and regional enterprises that offer long-term value, with the goal of delivering steady and sustainable returns to our shareholders.”Contact informationJune TuoTel: (852) 5983-9260Phone: (86)1392-3804-279Intelligent Joy Limited Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com