日期: 2026 年 2 月 5 日

香港, 2026年2月5日 - (亞太商訊 via SeaPRwire.com) - 根據香港聯交所披露的文件，新加坡政府投資公司（GIC Private Limited）入股歌禮製藥，以每股均價12.18港元，買入64,128,000股普通股股份，合計涉資約7.81億港元，折合約1億美元。入股完成後，GIC持有歌禮製藥64,128,000股股份，占公司已發行股本約6.42%，正式躋身公司主要機構股東行列。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月5日 - (亞太商訊 via SeaPRwire.com) - 由香港貿易發展局（香港貿發局）主辦的全球最大一站式珠寶商貿平台，將於3月初以「兩展兩地」的成功模式揭幕。第12屆香港國際鑽石、寶石及珍珠展於3月2至6日在亞洲國際博覽館舉行，展出各類珠寶原材料。第42屆香港國際珠寶展則於3月4至8日假灣仔香港會議展覽中心舉辦，展示各款珠寶首飾成品。香港貿發局副總裁古靜敏表示：「今屆珠寶雙展將雲集逾40個國家及地區、約4,000家展商，當中七成來自香港以外的地區，其中巴西、阿聯酋和印度展商更擴大參展規模，而烏茲別克更是首次參展。香港貿發局積極打造全球最大一站式珠寶商貿平台，凸顯香港作為國際商貿及珠寶採購中心的地位。」回顧環球珠寶市場，2025年本港貴重珠寶出口至東盟錄得51%升幅，而出口至英國、澳洲及瑞士的增長分別按年上升36%、28%及10%。兩展雲集逾40個展團 硬足金展館開啟金飾新篇章珠寶雙展一直備受環球業界支持，今年雲集超過40個展團，當中包括中國內地、台灣、印度、以色列、韓國、緬甸、新加坡、斯里蘭卡、泰國、烏茲別克、比利時、德國、意大利、西班牙、土耳其、巴西、哥倫比亞、墨西哥及美國等。世界黃金協會將首設硬足金展館，合共11家中國內地展商，向國際市場展示嶄新黃金技藝，目標以展會作「出海」平台，開拓環球商機。此外，今年香港表廠商會首次組團參展，來自湖北的竹山綠松石展團也首度亮相。而坦桑石協會、彩色寶石協會、亞太區創作師協會及亞洲珠寶文化設計工藝協會亦將繼續參展，香港珠寶玉石廠商會將聯同Italian Exhibition Group（IEG）再度設館，展示製造珠寶的最新設備和技術。國際品牌 矚目登場香港國際珠寶展的「品牌精粹廊」展區（Hall of Fame）載譽歸來，規模較去年增加逾四成，匯聚更多國際知名珠寶品牌；其中土耳其領先鑽石珠寶品牌 Zen Diamond（展位：CEC 3B-C12）將帶來採用精細裁切工藝的鑽戒系列。於「珠寶精粹廊」展區（Hall of Extraordinary），香港展商恒和鑽石（展位：CEC GH-C07）則展出一枚18K白金及玫瑰金鑲嵌藍鑽與淺彩粉鑽戒指。 另一香港展商Unique Brilliant Limited（展位：CEC GH-C13）將展示一套項鏈與耳環組合，紅寶石未經加熱處理，呈現珍稀的「鴿血紅」（pigeon blood red）色澤。東方美學展現非遺工藝今年展會雲集多款承載東方文化的珠寶。來自中國內地的廣東嘉寶閣傳世珠寶（展位：CEC GH-A16），帶來以國家級非遺工藝「花絲鑲金」，以人手製作的蝴蝶胸針，耗時逾四個月。另一內地展商賽菲爾珠寶（展位：CEC 3E-E02）則帶來了「宮廷新中式」風格的作品，運用六項古法黃金工藝製作而成，將傳統技藝展現在當代首飾上。內地近年興起硬足金技術，高純度和高硬度的特性，令金飾可以融入更多時尚和現代設計元素。由世界黃金協會舉辦的研討會將分析最新的黃金市場情況和硬足金技術。展會期間將舉行多場關於東方美學珠寶的活動。香港珠寶首飾業商會主辦的香港國際時尚足金飾設計比賽，鼓勵設計師創作出迎合東盟及中東年輕市場，兼具文化內涵和商業潛力的金飾作品，頒獎典禮將於展會期間舉行。由香港玉器商會主辦，首屆國際翡翠玉器首飾設計大賽2026亦會在展會期間舉行頒獎典禮。創意設計領潮流緊貼潮流及具創意的產品有助業界突圍而出。有展商將創新構思化成潮流產品，Austy Lee Company Limited（展位：CEC 1E-F32）趁馬年將至，推出以斑馬紋理為設計靈感的手鐲。今年「珠寶設計精選」展區（Designer Galleria）迎來新展商Zheng Hong Collective（展位：CEC 1CON-067A），帶來一款飛魚胸針，佩戴時翅膀和尾端會隨身體而擺動。今年香港珠寶設計比賽以「未琢之韻．自然之美」為題，啟發本地學生及業界精英以作品演繹大自然之美與設計故事，凸顯珠寶設計的多元面貌，大會將於展會期間公佈賽果。稀世瑰寶閃耀雙展兩展一直為買家網羅古典珍藏及稀有珠寶，香港國際珠寶展的香港展商拾璣古董珠寶（展位：CEC CH-F13）展出20 世紀、70 年代製作的布契拉提粉色藍寶石套裝。另有展商 World Coins Co., Ltd. （展位：CEC CH-N12）帶來19世紀意大利工匠的雙色琺琅鑽石首飾，首飾連同原盒完整保存至今超過100年。香港國際鑽石、寶石及珍珠展則有德國展商Caram e.K. （展位：AWE 8-F05）帶來18.98卡AGL認證、收藏級的天然粉紅藍寶石；加大拿展商Korite Ammolite Ltd（展位：AWE 8-F35）展示18K金AA級斑彩石配鑽石頸鍊。活動方面，香港國際珠寶展將舉行「珠寶風格從何而來？探究時代與工藝的印記」座談會，特別邀請英國著名歷史學家及珠寶權威 Dr. Jack Ogden主講，深入剖析珠寶工藝演進及時代審美變遷。逾20場論壇活動 探討AI及網絡營銷等業界熱話珠寶雙展期間將舉行超過20 場行業講座與交流活動，涵蓋行業趨勢、網絡營銷和珠寶科技等，其中香港國際珠寶展第二日將剖析人工智能如何由設計走到商業化，推動珠寶行業發展。另外大會將安排研討會，網紅分享如何利用電商平台提高珠寶品牌的影響力、增加銷售和實踐經驗等，讓業界加快打通線上線下的協同合作渠道。體驗與服務並重 全球買家首選平台展覽吸引環球大型珠寶零售連鎖店、高端、輕奢及設計師珠寶品牌到場採購，為買賣雙方締造商機，並推動業界交流。此外，香港貿發局為持續優化世界各地買家來港採購的體驗，聯同香港旅遊發展局及多家企業推出買家專屬優惠，涵蓋餐飲、機票、酒店等，讓參觀珠寶雙展的買家，同時感受香港獨有魅力。大會將安排免費穿梭巴士，接載買家往返亞洲國際博覽館及市區（包括灣仔香港會議展覽中心），詳情請參閱展會網站。線上線下相結合 便利入場洽商採購今年珠寶雙展將沿用「展覽+」（EXHIBITION+）線上線下融合模式，除了在展會現場採購，由2月23日至3月13日，「商對易」(Click2Match）的人工智能會為展商及買家提供線上商貿配對。在場買家則可利用「掃碼易」（Scan2Match）掃描展商的二維碼，於展會期間或之後隨時隨地於線上洽談。在買家入場方面，「香港貿發局商貿平台」流動應用程式（HKTDC Marketplace App）及兩展的官方網頁都提供網上驗證功能。買家只需透過上述平台登記、上傳照片和有效證件，即可獲取已驗證的買家證，無需現場排隊登記或驗證，大大提升採購效率。圖片下載︰https://bit.ly/4ayrcAo香港貿發局副總裁古靜敏（中）、香港貿發局珠寶業諮詢委員會主席周允成（左）以及香港貿發局香港國際珠寶展及香港貿發局香港國際鑽石、寶石及珍珠展籌備委員會主席黃紹基（右），出席今天（2月5日）舉行的香港國際珠寶展和香港國際鑽石、寶石及珍珠展新聞發佈會。古靜敏（前排左三）連同一眾香港貿發局香港國際珠寶展及香港國際鑽石、寶石及珍珠展籌備委員會委員，以及表演嘉賓合照。藝人陳曉華（右三）率領一眾模特兒演繹各款瑰麗珠寶。藝人陳曉華佩戴展商安東公司帶來的天然緬甸翡翠套裝，碧綠晶瑩的翡翠鑽石頸鏈、戒指及耳環，設計高貴優雅。鳳凰常見於中式婚嫁飾品，象徵吉祥、如意，展商老鳳祥帶來富有中式魅力的國潮婚嫁系列，打造女性宮廷般尊貴的飾品。相關網頁 香港國際珠寶展展覽網頁http://hkjewelleryshow.hktdc.com/tc兩展穿梭巴士安排https://www.hktdc.com/event/hkjewellery/tc/travel-to-fairground-hkcec展會活動https://www.hktdc.com/event/hkjewellery/tc/intelligence-hub  香港國際鑽石、寶石及珍珠展展覽網頁http://hkdgp.hktdc.com/tc兩展穿梭巴士安排https://www.hktdc.com/event/hkdgp/tc/travel-to-fairground-awe展會活動https://www.hktdc.com/event/hkdgp/tc/intelligence-hub香港貿發局新聞中心：http://mediaroom.hktdc.com/tc傳媒查詢香港貿易發展局傳訊及公共事務部：簡惠宜電話：(852) 2584 4055電郵：winnie.wy.kan@hktdc.org黃家欣電話：(852) 2584 4524電郵：katy.ky.wong@hktdc.org張敏萱電話：(852) 2584 4137電郵：jane.mh.cheung@hktdc.org香港貿易發展局簡介香港貿易發展局(香港貿發局)是於1966年成立的法定機構，負責促進、協助和發展香港貿易。香港貿發局在世界各地設有超過50個辦事處，其中13個設於中國內地，致力推廣本港作為雙向環球投資及商業樞紐。 香港貿發局通過舉辦國際展覽會、會議及商貿考察團，為企業(尤其是中小企)開拓內地和環球市場的機遇。香港貿發局亦通過研究報告和數碼資訊平台，提供最新的市場分析和產品資訊。有關香港貿發局的其他資訊，請瀏覽www.hktdc.com/aboutus/tc。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月5日 - (亞太商訊 via SeaPRwire.com) - 亞太地區燃油供應服務商萬利集團（以下簡稱（「萬利」或（「集團」）於2月2日舉辦以「開拓新視野：以可持續燃料推動綠色航運」為主題的首屆環境、社會與治理（ESG）論壇。論壇匯聚航運高管、金融家、法律專家及冰川學家，共同探討應對航運業迫切減碳挑戰的方案。以下演講嘉賓陣容於論壇探討關鍵議題，分享獨特見解：萬利集團主席兼行政總裁謝威廉博士 萬利集團獨立董事、Chooi & Company合夥人、馬來西亞大律師公會前會長及LAWASIA執行委員會委員謝依玲女士國泰世華銀行資本市場暨顧問部協理劉名軒先生 極地探險家、冰川學家及政策顧問、Polar Research and Expedition Consultancy創辦人／冰川學家與遠征總監張偉賢博士 滙豐香港工商金融可持續金融高級經理張雯瑾女士是次論壇為思想領袖提供了一個互動及對話的平台，並透過演講嘉賓的專題講座探討若干關鍵議題，包括氣候變化對全球航運的影響、持續轉變的可持續發展相關法規，及創新綠色及可持續發展掛鈎融資解決方案。謝威廉博士在主題演講中表示：「全球航運業正處於關鍵時刻，迅速轉變的監管法規、緊張的地緣政治局勢、氣候挑戰及技術發展正以前所未有的速度重塑行業格局。因此，我們期望打造一個協作環境，讓持份者聚首一堂，分享見解並制定策略，以構建可持續未來。」在論壇上，謝依玲女士討論ESG如何成為保障地球健康的法律、經濟和道德必要條件，並強調政府、企業、法院及資本市場必須在全球層面上通力合作，將可持續發展願景轉化為可量化的實際行動。謝女士表示：「我們必須建立全球健康指標體系，以系統追踪環境影響、健康影響及風險對全人類的綜合作用。這不僅需要量化工具評估進展，更需制定戰略傳播方案以提升全球認知、推動全民教育。同時，必須將指標體系深度融入組織、國家及國際治理架構，在本土和全球層面同步實施。企業應踐行負責任的商業倫理，全面對標ESG準則，構建普適性的全球健康框架。唯有通過全球協同標準化，方能實現框架的系統化落地與長效運行。」劉名軒先生分享其對將ESG特徵融入融資策略的見解：「綠色貸款（Green Loans）在企業擁有明確、具體的投資計劃時尤其適合。可持續發展掛鈎貸款（Sustainability-Linked Loans，SLLs）遵循獨特的邏輯：其關鍵績效指標（KPIs）必須反映重大的可持續議題，並且可量化、追踪和獨立驗證。最重要的是，可持續性績效目標（Sustainability Performance Targets，SPTs）必須在『積極進取』和『實際可行』之間取得平衡，確保在公司的運營能力範圍內有機會實現目標。與綠色貸款不同，SLLs不限制所得款項只用於綠色活動上；相反，SLLs通過與績效掛鈎的金融機制展示可持續承諾。除了貸款和債券，幾乎所有負債型金融産品現在都可以加入綠色或可持續性元素。這種靈活性使得企業能夠將融資與可持續目標結合在一起，一方面保持運營的實際可行性，也能推動環境進步與金融創新。」張偉賢博士分享其對地球科學教育與倡導的堅定承諾，並探討航運業的負責任發展機遇：「航運行業的可持續發展機遇始於認識到北極不僅是一條捷徑，更是一個生機勃勃的家園和地球脆弱的氣候調節器。新開通的極地航綫雖能縮短運輸時間、降低燃油消耗，但其航經水域存在基礎設施匱乏、生態系統脆弱、原住民依賴海冰維繫文化與生存等挑戰。真正的領導力意味著要投資於更清潔的燃料、冰級船舶和強化搜救能力，同時嚴格限制黑碳排放（Black Carbon Reduction），並尊重國際極地法規。這也意味著傾聽在冰上安全旅行了數千年的地方知識，並將這種智慧與現代科學和衛星數據融合。如果行業將ESG原則嵌入到每一次北極航行中，這些新興航綫能夠成為可持續創新的典範，而非不受控制風險的新邊界。」張雯瑾女士從可持續金融角度分享航運業轉型趨勢：「監管不斷變化，應對氣候目標和實現可持續海洋運輸的策略亦需要與時並進。目前，創新方案也應運而生，船東群體正探索生物燃料、生物液化天然氣（bio-LNG）、生物沼氣等替代能源方案。清潔技術研發持續，有助推動全球航運業向可持續模式的系統性轉型。」論壇在與會人士熱烈交流中圓滿結束，除交流意見外，他們亦重申對推動航運業可持續發展的共同承諾。萬利集團在可持續發展領域的領導地位突出，顯示其在引領行業減碳與推行負責任實踐方面的不懈努力。集團亦透過參與EcoVadis永續性評級系統及支持多元化可持續船用燃料，持續推進航運業的有效轉型。展望未來，集團將繼續舉辦更多論壇，促進對話交流、創新及合作，從而建立更可持續的海洋生態系統。謝威廉博士補充：「以上不過是個開端，萬利將繼續為行業及客戶制定切實可行的減碳解決方案。」有關萬利集團及其可持續發展方案的更多訊息，請瀏覽 www.banle-intl.com。圖片說明1：謝威廉博士（中）向演講嘉賓及論壇成員致送紀念品以示感謝。圖片說明2：論壇成員就「開拓新視野：以可持續燃料推動綠色航運」主題進行討論。謝依玲女士（左）擔任主持人，引領討論並以論壇成員身份分享見解。圖片說明3 ：與會人士在 ESG 論壇上聚集，展現了對航運業可持續實踐和創新解決方案的共同承諾。關於萬利集團萬利集團成立於 2015 年，以CBL International Limited（納斯達克：BANL）在納斯達克股票市場上市。我們致力於為客戶提供一站式燃油供應服務，被業內稱為燃油供應服務商。我們主要通過當地實體供貨商為船舶提供燃油加注服務，遍布比利時、中國、香港、印度、日本、韓國、馬來西亞、毛里裘斯、巴拿馬、菲律賓、新加坡、台灣、泰國、土耳其和越南，共覆蓋65個港口。集團積極推動可持續燃料，並已取得ISCC EU和ISCC Plus認證，以及EcoVadis銀獎。如欲瞭解更多信息，請到集團網站 https://www.banle-intl.com  瀏覽。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

HONG KONG, Feb 5, 2026 - (ACN Newswire via SeaPRwire.com) – Banle Group (“Banle” or the “Group”), a leading Asia-Pacific marine fuel logistics provider, hosted its landmark inaugural ESG Forum — "Charting the New Horizon: Powering Green Shipping with Sustainable Fuels" — uniting top maritime executives, financiers, legal experts, and climate scientists to address the shipping industry's urgent decarbonization challenges on February 2.Speaker Lineup Tackles Critical IssuesThe forum featured exclusive insights from:Dr. Teck Lim Chia, Chairman and CEO of Banle GroupMs. Karen Cheah Yee-Lynn, Independent Director of Banle Group, Partner of Chooi & Company, Immediate Past President of the Malaysian Bar and EXCO Member of LAWASIAMr.Matt Liu Ming-Hsuan, SVP Capital Solutions, Cathay United BankDr.Wilson Cheung Wai-yin, Polar Explorer, Glaciologist and Policy Advisor, Polar Research and Expedition ConsultancyMs.Rebecca Zhang, Senior Manager Sustainable Finance, Commercial Banking, Hong Kong, HSBCThe forum served as a dynamic platform for thought leadership and dialogue, featuring a series of presentations addressing critical topics such as the impact of climate change on global shipping, evolving sustainability-related regulations, and innovative green and sustainability-linked financing solutions.Dr.Teck Lim Chia addressed in the keynote speech, “The global shipping industry stands at a pivotal moment. Rapid regulatory changes, geopolitical tensions, climate challenges, and technological advancements are reshaping the landscape at unprecedented speed. Yet, we are dedicated to fostering a collaborative environment where stakeholders can come together to share insights and develop strategies for a more sustainable future.”On the forum, Ms.Karen Cheah talked about how ESG has become a legal, economic, and moral imperative to safeguard planetary health – and how governments, businesses, courts, and capital markets at an international level must work together holistically to turn sustainability from aspiration into measurable action. She said, “We must establish planetary health metrics to track environmental, health, and risk impacts on all of us. This requires not only a measurement to gauge our progress but also a strategic plan to communicate these metrics, drive global awareness, and educate society at large. Moreover, we must integrate these metrics into governance structures at organizational, domestic, national, and international levels. We must engage in responsible business practices aligned with ESG components and ensure a robust framework for planetary health is implemented globally. Once we align collectively, we can systemize this framework for lasting impact.”Mr.Matt Liu shared his insight on integrating ESG features into financing strategies, “Green loans excel when companies have a clear, specific investment plan. Sustainability-Linked Loans (SLLs) operate under a distinct logic: their Key Performance Indicators (KPIs) must reflect material sustainability issues, be measurable, traceable, and independently verifiable. Crucially, Sustainability Performance Targets (SPTs) must balance ambition with feasibility, remaining achievable within the company’s operational capacity. Unlike green loans, SLLs do not restrict proceeds to green activities; instead, they demonstrate sustainability commitment through performance-linked financial mechanisms. Beyond loans and bonds, nearly all liability-style financial products can now integrate green or sustainability elements. This flexibility allows companies to align financing with sustainability goals while maintaining operational practicality, driving both environmental progress and financial innovation.”Dr.Wilson Cheung addressed his dedication to geoscientific education and advocacy, and talked about the responsible opportunities for the shipping industry, “Responsible opportunities in the shipping industry begin with recognising that the Arctic is not only a shortcut, but also a living homeland and a fragile climate regulator for the planet. New polar sea routes can reduce transit time and fuel use, yet they cross waters where infrastructure is scarce, ecosystems are vulnerable, and Indigenous communities depend on sea ice for culture and survival. True leadership means investing in cleaner fuels, ice-class vessels, and robust search-and-rescue capacity, while strictly limiting black carbon emissions and respecting international polar regulations. It also means listening to local knowledge that has guided safe travel on ice for thousands of years and integrating that wisdom with modern science and satellite data. If the industry embeds ESG principles into every Arctic voyage, these emerging routes can become a model of responsible innovation rather than a new frontier of unchecked risk.”Ms.Rebecca Zhang shared recent shipping industry transition trends from a sustainable finance perspective: “Regulations are constantly evolving, and so must global efforts to tackle climate change and make maritime transport more sustainable. Innovative solutions are emerging, and shipowners are exploring alternative energy options such as biofuels, bio-LNG, and bio-gas. The development of clean technologies is accelerating the industry’s systemic shift towards sustainability.”The forum concluded with a lively and interactive networking among participants, who exchanged ideas and reaffirmed their collective commitment to advancing sustainable practices throughout the shipping industry.Banle Group's sustainability leadership by example through its operational practices was prominently showcased, highlighting its ongoing efforts to spearhead industry decarbonization and responsible practices. Through initiatives like its participation in the EcoVadis rating system and advocacy for diverse sustainable marine fuels, Banle continues to drive meaningful transformation across the shipping sector.Looking ahead, the Banle Group remains committed to hosting future forums that foster dialogue, innovation, and collaboration for a more sustainable maritime ecosystem.Dr.Teck Lim Chia added: "This is just the beginning. Banle will continue driving practical decarbonization solutions for our industry and clients."For more information about Banle Group and its sustainability initiatives, please visit www.banle-intl.com.Photo Caption 1: Dr. Teck Lim Chia (centre) presented souvenirs to all speakers and panelists as a token of appreciation.Photo Caption 2: Panelists engaged in a discussion on the theme: “Charting the New Horizon: Powering Green Shipping with Sustainable Fuels”. Ms. Karen Cheah (left) served as moderator, guiding the discussion while also contributing her insights as a panelist.Photo caption 3: Attendees gathered at the ESG Forum, showcasing a shared commitment to sustainable practices and innovative solutions in the shipping industry.About Banle GroupCBL International Limited (Nasdaq: BANL) is the listing vehicle of Banle Group, a reputable marine fuel logistics company based in the Asia Pacific region that was established in 2015. We are committed to providing customers with a one-stop solution for vessel refueling, which is referred to as bunkering facilitator in the bunkering industry. We facilitate vessel refueling mainly through local physical suppliers in 65 major ports covering Belgium, China, Hong Kong, India, Japan, Korea, Malaysia, Mauritius, Panama, the Philippines, Singapore, Taiwan, Thailand, Turkey and Vietnam. The Group actively promotes the use of sustainable fuels and has been awarded the ISCC EU and ISCC Plus certifications, as well as EcoVadis Silver Medal.For more information, please visit: https://www.banle-intl.com. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

BRISBANE, AUS, Feb 5, 2026 - (ACN Newswire via SeaPRwire.com) - Annature, Australia's leading eSignature and Identity verification provider, has announced the release of its 21 CFR Part 11 compliant electronic signature module, enabling organisations operating in FDA‑regulated environments to execute electronic records with confidence.The new capability ensures Annature customers can meet the U.S. Food and Drug Administration's requirements for electronic records and electronic signatures under 21 CFR Part 11, a regulation that governs data integrity, signer authentication, and auditability across industries such as life sciences, pharmaceuticals, biotechnology, and clinical research.The release has been driven by growing demand from U.S.-based and multinational organisations seeking a modern, compliant alternative to legacy eSignature platforms. Several customers operating in regulated environments have already transitioned to Annature as part of broader digital transformation initiatives, prompting the company to formally introduce Part 11 support as part of its international product roadmap."As we continue to grow globally, it's critical that Annature supports the regulatory frameworks our customers operate under," said Corey Cacic, CEO of Annature. "Our 21 CFR Part 11 module allows organisations subject to FDA requirements to use Annature with confidence, knowing their electronic signatures meet the necessary compliance standards."The module introduces controls aligned with Part 11 expectations, including secure signer authentication, tamper‑evident audit trails, and strong linkage between electronic signatures and the records they relate to. These features ensure electronic signatures executed through Annature can be relied upon in regulated workflows and during regulatory review.Kim Steel, Founder and Managing Director of SAPRO - a boutique CRO supporting niche biotech and pharmaceutical companies with commercially sponsored Phase I-III full-service clinical trials has welcomed the release."For organisations operating in regulated environments, compliance with 21 CFR Part 11 is not optional - it is fundamental," said Steel. "It is encouraging to see Annature, an Australian technology provider supporting international regulatory requirements that are critical to our industry and our clients. Solutions like this enable sponsors to operate confidently on a global stage, without reliance on outdated or overly complex legacy systems, while remaining inspection and audit-ready at all times."The launch further strengthens Annature's position as a global‑ready eSignature platform, supporting organisations that operate across jurisdictions with varying compliance obligations. The 21 CFR Part 11 module is available now and can be enabled for customers who require FDA‑compliant electronic signatures.About AnnatureAnnature is Australia's leading eSignature and Identity verification provider, trusted by over 6,700 businesses. With a Pay as you go model and deep integration across the business app ecosystem, Annature delivers secure, affordable, and locally supported solutions for professionals across the country. Annature's growing product suite also includes integrated payments and compliance features designed to support both domestic and international regulatory requirements.https://www.annature.com.auCONTACT:Name: Corey CacicEmail: corey@annature.com.auSOURCE: Annature Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

MORTSEL, BE, Feb 5, 2026 - (ACN Newswire via SeaPRwire.com) - AGFA HealthCare today announced that it has been named Best in KLAS® 2026 across three Enterprise Imaging segments in the United States, with two awards earned for the second consecutive year, underscoring the company's continued leadership in delivering clinician-first imaging solutions trusted by healthcare organizations worldwide.The recognition comes as KLAS Research marks its 30th anniversary, celebrating three decades of amplifying the voice of healthcare providers through independent, data-driven insights.AGFA HealthCare's Best in KLAS distinctions reflect strong customer validation of its Enterprise Imaging platform - designed to empower clinicians to stay in their flow, reduce complexity across imaging workflows, and enable confident clinical decision-making through connected, high-performing access to images and data.Best in KLAS® - Enterprise Imaging (United States)Enterprise Imaging for Radiology: ranked #1 with a 93.2% score in the PACS (Small - under 300k studies) segment.XERO® Viewer: ranked #1 with a 92.1% score in the Universal Viewer (Imaging) segment for the third consecutive yearEnterprise Imaging VNA: ranked #1 with a 89.8% score in the Vendor Neutral Archive (VNA) segment for the second consecutive year."Being recognized across three Enterprise Imaging segments - including multiple consecutive wins - is a powerful affirmation of our clinician-first strategy," said Nathalie McCaughley, President of AGFA HealthCare. "Healthcare organizations trust us to deliver imaging environments that truly support clinicians in their daily work, while enabling IT and clinical leaders to operate with confidence, performance, and long-term vision. This recognition reflects the strength of our partnerships and our unwavering focus on empowering care teams through connected, intelligent imaging."Commenting on the awards, Adam Gale, CEO of KLAS Research, said:"The Best in KLAS winners have earned the trust of their customers over the past year. With this recognition, they set the standard for excellence through partnership in healthcare technology and services in the months to come."Monique Rasband, Global Vice President of Imaging at KLAS Research, added:"AGFA HealthCare's strong performance across multiple Enterprise Imaging segments reflects consistent customer feedback. Organizations recognize the value of solutions that help imaging teams work efficiently today while providing a clear path for future growth and innovation."The Best in KLAS awards are based on direct feedback from healthcare providers and recognize vendors who consistently demonstrate excellence through partnership, performance, and responsiveness to customer needs.AGFA HealthCare will celebrate its Best in KLAS recognition during HIMSS 2026, alongside customers and partners, as part of its continued commitment to advancing connected, intelligent, and human-centered imaging at scale.KLAS referencesBest in KLAS Awards overview: 2026 Best in KLAS Awards: Software and Services ReportEnterprise Imaging segments reports: 2026 Best in KLAS Awards: Software and Services ReportAbout AGFA HealthCareAt AGFA HealthCare, we understand that striking the critical balance between clinical efficiency and quality patient care starts with the clinician experience. We recognize how vital it is for clinicians to be fully immersed in their cases, channeling all their energy into delivering confident, informed diagnoses. That's why we designed our Enterprise Imaging platform to eliminate the barriers that get in the way. When distractions melt away, technology feels like an extension of one's thought process, and each clinician has everything they need to perform at the top of their craft. That's life in flow.This belief shapes everything we do - guided by our Mission, Vision, and Customer Delivery Principles, which are designed to empower clinicians and elevate their experience.AGFA HealthCare is a division of the Agfa-Gevaert Group. For more information on AGFA HealthCare, please visit www.agfahealthcare.comand follow us on LinkedIn.AGFA and the Agfa rhombus are registered trademarks of Agfa-Gevaert N.V. Belgium or its affiliates. XERO is a registered trademark of Agfa HealthCare N.V. Belgium or its affiliates. All information contained herein is intended for guidance purposes only, and the characteristics of the products and services described in this publication can be changed at any time without notice. Products and services may not be available for your local area. Please contact your local sales representative for availability information. AGFA HealthCare diligently strives to provide as accurate information as possible but shall not be responsible for any typographical error.About KLAS ResearchKLAS Research is a leading healthcare IT data and insights company dedicated to improving global healthcare delivery by amplifying the voice of healthcare providers. Celebrating its 30th anniversary in 2026, KLAS evaluates vendor performance through independent research based on direct customer feedback.Best in KLAS® is a registered trademark of KLAS Research.Press Contact: Jessica Baldry, Global Marketing & Communications Manager, AGFA HealthCare +44 1206 413052 jessica.baldry@agfa.comSOURCE: Agfa HealthCare Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

OSAKA, Japan, Feb 5, 2026 - (ACN Newswire via SeaPRwire.com) – February 4, 2026, SuperX Industries Co., Ltd. ("SuperX"), a Japanese subsidiary of SuperX AI Technology Limited (“NASDAQ:SUPX”), today announced the signing of an Memorandum of Understanding ("MOU") on February 4, 2026 with Digital Dynamic Inc. ("DD"), eole Inc. ("eole"), and Woodman Inc. ("Woodman"). This MOU builds on the parties’ prior cooperation to establish a comprehensive framework for the co-development of large-scale AI Data Centers (AIDC) across Japan.Advancing the Mie Prefecture Pilot ProjectFollowing the first MOU signed on January 30, 2026 in Osaka, Japan, the Parties entered into the MOU to further deepen collaboration by establishing a joint task force to pilot an AIDC project in Mie Prefecture, Japan with an initial facility capacity up to 4MW, subject to feasibility assessments, site conditions, regulatory approvals, and the execution of definitive agreements. The pilot initiative is intended to serve as a starting point for assessing potential future expansion up to 300MW in total capacity.Addressing Japan’s AI Infrastructure BottleneckThe shift toward modular architecture directly addresses Japan’s growing demand for the expansion of domestic AI capacity on an accelerated timeline. Unlike traditional "brick-and-mortar" builds that can take years to complete, SuperX’s modular approach accelerates deployment by reducing construction timelines significantly. This new pilot project is designed to be purpose-built for next-generation, liquid-cooled GPUs—capabilities often lacking in legacy data centers.Scalable delivery and reliable operationsPursuant to the MOU, the Parties intend to collaborate on the system-level integration of critical infrastructure, including advanced power systems and liquid cooling solutions essential for continuous AI workloads. The framework also contemplates the future integration of renewable energy components, such as solar and wind power, energy storage systems, and grid interconnection, subject to site conditions, commercial viability and regulatory approvals.To facilitate execution, a joint task force is expected to be established to define technical architecture, governance, and near-term milestones. SuperX will lead the provision of the modular system architecture and power system integration.Executive quote“Speed-to-market is the new currency in the AI race,” said Aiko Furukawa, the CEO of SuperX Industries Co. Limited. “This pilot project in Mie Prefecture is intended to demonstrate how we can deploy AI infrastructure with speed. Alongside our partners, we aim to demonstrate that modular scalability is the most viable path to meeting Japan's surging demand for AI.”Looking aheadLooking forward, the Parties intend to use the initial pilot as a reference framework to evaluate broader modular AIDC opportunities across Japan, including scalable pathways for expansion—subject to further feasibility assessments, regulatory approvals, site conditions, and the negotiation and execution of definitive agreements.About Digital Dynamic IncDigital Dynamic Inc. is one of Japan’s fastest-growing AI infrastructure operators, with a rapidly expanding deployment of NVIDIA-based inference GPU resources. In 2026, the company plans to complete AI data centers in Kagoshima Prefecture and Fukushima Prefecture, reinforcing Japan’s next-generation AI computing foundation.About eole Inceole Inc. is a publicly listed company in Japan with a rapidly growing presence in the domestic GPU server market. The company provides investment and business development support for AI data center development projects, playing an active role in advancing Japan’s AI infrastructure ecosystem.About Woodman IncWOODMAN Inc. is a Japanese technology company focusing on eliminating societal waste by transforming underutilized resources, such as surplus electricity and computing power, into new value. They specialize in constructing optimized computing environments for AI and HPC (High-Performance Computing), bridging the gap between energy infrastructure and, previously, blockchain/mining hardware.About SuperX AI Technology Limited (NASDAQ:SUPX)SuperX AI Technology Limited is an AI infrastructure solutions provider, offering a comprehensive portfolio of proprietary hardware, advanced software, and end-to-end services for AI data centers. The Company's services include advanced solution design and planning, cost-effective infrastructure product integration, and end-to-end operations and maintenance. Its core products include high-performance AI servers, 800 Volts Direct Current (800VDC) solutions, high-density liquid cooling solutions, as well as AI cloud and AI agents. Headquartered in Singapore, the Company serves institutional clients globally, including enterprises, research institutions, and cloud and edge computing deployments. For more information, please visit www.superx.sgSafe Harbor Statement This press release may contain forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as "may," "should," "expects," "anticipates," "contemplates," "estimates," "believes," "plans," "projected," "predicts," "potential," or "hopes" or the negative of these or similar terms. In evaluating these forward-looking statements, you should consider various factors, including: our ability to change the direction of the Company; our ability to keep pace with new technology and changing market needs; and the competitive environment of our business. These and other factors may cause our actual results to differ materially from any forward-looking statement.Forward-looking statements are only predictions. The reader is cautioned not to rely on these forward-looking statements. The forward-looking events discussed in this press release and other statements made from time to time by us or our representatives, may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us. We are not obligated to publicly update or revise any forward-looking statement, whether as a result of uncertainties and assumptions, the forward-looking events discussed in this press release and other statements made from time to time by us or our representatives might not occur. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

Shanghai, January 5, 2026 - (ACN Newswire via SeaPRwire.com) – Everest Medicines (HKEX 1952.HK, "Everest", or the "Company"), a biopharmaceutical company focused on the discovery, clinical development, manufacturing, and commercialization of innovative therapeutics, today announced that it has entered into an exclusive license agreement with Shaanxi Micot Pharmaceutical Technology Co., Ltd. (“Micot”) to commercialize MT1013, the world’s first-in-class dual-targeting receptor agonist polypeptide that simultaneously targets the Calcium-Sensing Receptor (CaSR) and the Osteogenic Growth Peptide (OGP) receptor and is primarily developed with Secondary Hyperparathyroidism (SHPT) as its leading indication, in China and Asia-Pacific (excluding Japan).According to the agreement, Everest Medicines will pay Micot an upfront payment of RMB 200 million and potential regulatory and commercial milestone payments of up to RMB 1,040 million. MT1013 has entered Phase III clinical trial in China and the relevant development expenses will be covered by Micot. The strategic collaboration is expected to complement Everest Medicines’ existing renal pipeline and drive operating synergies, further strengthen the Company’s commercial product portfolio, and solidify its leading position in renal and autoimmune diseases in Asia, which are key therapeutic areas of focus. The collaboration will also expand the Company’s nephrology portfolio from IgA nephropathy to a broader range of chronic kidney diseases (CKD).MT1013 is the world’s first-in-class dual-targeting receptor agonist polypeptide internally developed by Micot. The Phase II data were presented orally and in a Late-Breaking session at the 2025 American Society of Nephrology (ASN) Annual Meeting. MT1013 uniquely combines the calcium-sensing receptor (CaSR) and the osteogenic growth peptide (OGP) receptor, addressing imbalances in parathyroid hormone (PTH), calcium, and phosphate metabolism. This innovative dual mechanism allows MT1013 to control SHPT and related bone metabolism disorders at the source, and to actively promote bone formation and repair through direct activation of osteogenic pathways, representing a therapeutic innovation shift from indirect inhibition of bone resorption to active stimulation of bone formation.Clinical studies have demonstrated that MT1013 acts rapidly, with strong and durable efficacy, and has a favorable safety profile in patients with CKD on maintenance hemodialysis with SHPT. It has shown potential advantages over current therapies in achieving comprehensive endpoints, including control of intact parathyroid hormone (iPTH), serum calcium, and phosphate levels, as well as improving calcium-phosphate balance and offering potential cardiovascular benefits. MT1013 is currently being evaluated in a Phase III clinical trial in China for this patient population, with over 50% of the target enrollment already achieved. SHPT is one of the most common and serious complications in patients with CKD. It causes disturbances in calcium and phosphate metabolism, elevated PTH levels, bone disorders, and vascular calcification, which substantially increase the risk of fractures, cardiovascular events, and mortality. SHPT is therefore an important factor influencing outcomes and prognosis in patients with CKD. With the global prevalence of CKD continuing to rise, the unmet medical need for effective SHPT therapies is also growing. Data indicate that the global population of patients with CKD has increased from 905.2 million in 2019 to 1.0655 billion in 2024 and is projected to exceed 1.2 billion by 2030 and 1.5 billion by 2035. Over the same period, the number of patients with SHPT has also continued to rise and is expected to reach approximately 189.9 million by 2030 and 221.7 million by 2035, highlighting a substantial and growing unmet medical need.“We are very pleased to collaborate with Micot. As the global burden of chronic kidney disease continues to rise, addressing patients’ unmet needs remains a top priority.,” said Mr. Yifang Wu, Chairman of the Board of Everest Medicines. “MT1013 represents an innovative asset with the potential to expand treatment options for patients with secondary hyperparathyroidism. Through this partnership, we aim to leverage our expertise in autoimmune-related kidney disorders while broadening our renal portfolio to include additional diseases, including glomerulonephritis and complications associated with dialysis. Looking ahead, we will jointly advance the development and commercialization of MT1013 to bring innovative treatment options to a broader population of patients with kidney disease.”“We are delighted to enter into this strategic collaboration with Everest Medicines. Everest’s deep expertise in nephrology and established commercialization capabilities make it an ideal partner to bring MT1013 to patients in China and beyond,” said Dr. Bing Wang, Founder, Chairman, and President of Micot. “MT1013 is a pivotal achievement of our peptide technology platform and a key milestone in our commitment to advancing innovative therapies for chronic diseases. Its unique dual-targeting mechanism has the potential to deliver meaningful advances in the treatment of secondary hyperparathyroidism. We look forward to working closely with Everest to accelerate clinical development and commercialization, address critical unmet medical needs, and advance care for patients with kidney disease.”MT1013 has completed its pivotal Phase II clinical trial, which demonstrated robust and sustained iPTH suppression in patients with SHPT undergoing maintenance hemodialysis. In head-to-head comparisons with etelcalcetide, MT1013 showed advantages in comprehensive disease management, achieving higher rates of simultaneous control of iPTH, serum calcium, and phosphate, as well as greater reductions in phosphate and the cardiovascular risk marker FGF-23. Over 52 weeks of treatment, MT1013 also resulted in significant improvements in bone mineral density and bone metabolism markers, supporting the potential clinical benefits of its unique dual-target mechanism in both disease management and bone health.Building on these positive results, the Phase II data were presented orally and in a Late-Breaking session at the 2025 American Society of Nephrology Annual Meeting. MT1013 has now advanced into a confirmatory Phase III clinical trial in China with cinacalcet as the active comparator. The Phase III study has been launched across more than 100 sites nationwide, aiming to enroll approximately 424 patients, specifically targeting individuals with SHPT undergoing maintenance hemodialysis due to chronic kidney disease.About MT1013MT1013 is the world’s first-in-class dual-targeting receptor agonist polypeptide that simultaneously targets the Calcium-Sensing Receptor (CaSR) and the Osteogenic Growth Peptide (OGP) receptor and is primarily developed with Secondary Hyperparathyroidism as its leading indication and is planned to expand into additional indications including Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD) with Osteoporosis and SHPT not on Dialysis. MT1013 completed its Phase II clinical trial (MT1013-II-C01) for the treatment of SHPT in May 2025 and has entered a Phase III clinical trial using Cinacalcet as the active comparator.About Everest MedicinesEverest Medicines is a biopharmaceutical company focused on discovering, developing, manufacturing and commercializing innovative pharmaceutical products that address critical unmet medical needs for patients in global markets. The management team of Everest Medicines has deep expertise and an extensive track record both in China and with leading global pharmaceutical companies.The Company’s therapeutic areas of focus include autoimmune, ophthalmology, critical care, and CKM (cardiovascular, kidney, and metabolic) diseases. Everest Medicines has developed a fully integrated commercialization platform that combines omnichannel commercial capabilities with end-to-end product lifecycle management. Leveraging its proprietary mRNA platform, the Company is advancing its existing pipeline, including mRNA in vivo CAR-T and mRNA cancer vaccines, while selectively expanding into additional high-value therapeutic areas with blockbuster potential, and accelerating its global expansion. For more information, please visit the Company’s website: www.everestmedicines.com.About MicotShaanxi Micot Pharmaceutical TechnologyCo., Ltd.("Micot") was founded in Xi’an in January 2007 and now operates in China (Xi’an, Suzhou, Beijing, Shanghai, Hong Kong) and the U.S. An R&D-driven innovator, Micot develops dual- and multi-functional peptide drugs for cardiovascular/cerebrovascular and metabolic diseases to address unmet clinical needs.As the proposer, implementer, validator, and developer of the bispecific peptide concept, Micot stands as a premier platform for peptide drug R&D. It utilizes a unique mechanism for screening multi-target peptide therapeutics and possesses platform-based R&D capabilities to develop both First-in-class and Best-in-class candidates.Currently, Micot has a robust reserve of new drug candidates, with seven proprietary innovative pipelines currently in clinical stage: one in Phase III, three in Phase II, and three in Phase I. Dedicated to creating breakthrough medicines and saving lives, Micot strives to address unmet clinical needs and leverages scientific innovation to safeguard human health. For more information, please visit the website: www.micot.cn.Forward-Looking StatementsThis news release may make statements that constitute forward-looking statements, including descriptions regarding the intent, belief or current expectations of the Company or its officers with respect to the business operations and financial condition of the Company, which can be identified by terminology such as “will,” “expects,” “anticipates,” “future,” “intends,” “plans,” “believes,” “estimates,” “confident” and similar statements. Such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, or other factors, some of which are beyond the control of the Company and are unforeseeable. Therefore, the actual results may differ from those in the forward-looking statements as a result of various factors and assumptions, such as future changes and developments in our business, competitive environment, political, economic, legal and social conditions. The Company or any of its affiliates, directors, officers, advisors or representatives has no obligation and does not undertake to revise forward-looking statements to reflect new information, future events or circumstances after the date of this news release, except as required by law. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

上海, 2026年2月5日 - (亞太商訊 via SeaPRwire.com) - 雲頂新耀（HKEX 1952.HK，以下簡稱「公司」），一家專注於創新藥研發、臨床開發、制造及商業化的生物制藥公司，今日宣布與陝西麥科奧特醫藥科技股份有限公司（以下簡稱「麥科奧特」）簽署獨家商業化許可協議，獲得MT1013在中國及亞太區（日本除外）的獨家商業化授權。MT1013為全球首創的雙靶點受體激動劑多肽，可同時靶向鈣敏感受體(CaSR)及成骨生長肽(OGP)受體，開發主要用於治療繼發性甲狀旁腺功能亢進症(SHPT)。此次戰略合作將與雲頂新耀現有腎科管線形成協同效應，強化產品佈局，鞏固公司在亞洲腎髒及自身免疫疾病領域的領導地位，並將產品覆蓋從IgA腎病拓展至更廣泛的慢性腎髒病領域。根據協議，雲頂新耀將向麥科奧特支付人民幣2億元首付款，以及最高不超過人民幣10.40億元的潛在監管及商業里程碑付款。中國III期臨床研究正在進行中，相關臨床開發費用將由麥科奧特承擔。MT1013是由麥科奧特自主研發的全球首創雙靶點多肽新藥，2025年獲美國腎髒病學會（ASN）年會「Late-Breaking」收錄。其開創性地融合了「鈣敏感受體（CaSR）+成骨生長肽（OGP）模擬」雙重作用機制，解決了PTH、鈣、磷代謝平衡的問題，這一全新設計使其在治療繼發性甲狀旁腺功能亢進（SHPT）及相關骨代謝疾病時，首次創造性的從源頭上控制病情，且能通過直接激活成骨通路，主動促進骨形成與修複，實現從「間接抑制骨吸收」到「主動促進骨生成」的治療創新升級。臨床研究證實，MT1013在慢性腎病接受維持性血液透析伴繼發性甲狀旁腺功能亢進患者中，起效迅速、效力強且持久，安全性良好，在綜合達標率（iPTH, 血鈣，血磷均達標）、血鈣鈣化指標的控制及心血管獲益前景上均展示出超越現有療法的潛力。目前，MT1013正在中國開展針對該患者群體的III期臨床研究，已入組超50%。SHPT是慢性腎髒病（CKD）患者最常見的嚴重並發症之一。該疾病導致鈣磷代謝紊亂、甲狀旁腺激素升高、骨病變、血管鈣化等一系列病理變化，顯著增加骨折、心血管事件和死亡風險，是影響CKD患者預後的關鍵因素。隨著全球慢性腎髒病患者規模持續擴大，SHPT及其相關治療需求亦不斷增長。數據顯示，全球CKD患者人數已由2019年的9.052億人增至2024年的10.655億人，預計2030年將超12億人，2035年將超15億人；同期全球SHPT患者人數亦持續增長，預計2030年將達約1.899億人，2035年將達約2.217億人，臨床需求亟待滿足。雲頂新耀董事會主席吳以芳表示：「我們非常高興能與麥科奧特達成此次合作。在全球慢性腎髒病患者持續增加的背景下，繼發性甲狀旁腺功能亢進仍存在顯著臨床未滿足需求。MT1013作為具備全球首創雙重作用機制的臨床後期創新資產，有望為SHPT患者提供全新的治療選擇。作為潛在同類最佳藥物，MT1013將與公司現有的腎科產品組合形成高度協同，進一步夯實公司在腎科領域的佈局。雲頂新耀在持續深耕自身免疫相關腎髒疾病的基礎上，正加速拓展至腎小球腎炎以及慢性腎髒病及其並發症等更廣泛的治療領域。此次合作是公司完善創新管線、拓展腎科治療邊界的重要戰略舉措，標志著腎科戰略由聚焦單一疾病領域向系統化和平台化的發展階段升級。未來，雙方將協同推進MT1013的開發與商業化，為更廣泛的腎病患者提供創新治療選擇。」麥科奧特創始人、董事長王冰博士表示：「我們很高興與雲頂新耀達成此次戰略合作。雲頂新耀在腎病領域擁有深厚的市場積累和成熟的商業化體系，是推動MT1013惠及中國乃至全球患者的理想合作夥伴。MT1013是公司多肽技術平台的重要成果，代表著公司在慢病創新治療領域深耕的重要里程碑達成，其獨特的雙靶點機制有望為SHPT治療帶來突破和更多獲益。我們期待與雲頂新耀緊密協作，加速該產品的臨床開發和上市進程，共同滿足廣大未滿足的臨床需求，開啟腎病領域治療的全新篇章。」MT1013已完成關鍵II期臨床研究，數據顯示，MT1013在維持性血液透析伴SHPT患者中，展現出強效且持久的iPTH抑制能力，並在與依特卡肽頭對頭比較中實現了綜合管理的優勢——其iPTH、血鈣、血磷三項同時達標率更高，降磷及降低心血管風險標志物FGF-23的優勢更強，加之MT1013在長達52周的治療中也為患者人群帶來了顯著的骨密度提升及骨代謝標志物改善，逐步驗證了其獨特的雙重機制在SHPT患者中綜合管理及改善骨骼健康方面的潛在臨床獲益。目前MT1013已進入以西那卡塞為陽性對照的確證性III期臨床試驗。該III期試驗已在全國範圍內啟動超過100家研究中心，計劃招募約424名患者，主要針對慢性腎髒病維持性血液透析伴 SHPT的患者群體。關於MT1013MT1013為全球首創的雙靶點受體激動劑多肽，可同時靶向鈣敏感受體（CaSR）及成骨生長肽（OGP）受體，開發主要用於治療繼發性甲狀旁腺功能亢進症（SHPT），並計劃拓展至包括慢性腎病性礦物質和骨代謝異常（CKD-MBD）伴骨質疏松及未接受透析的SHPT在內的額外適應症。MT1013已於2025年5月完成針對SHPT的II期臨床研究（MT1013-II-C01），並已進入以西那卡塞為對照的III期臨床研究。關於雲頂新耀雲頂新耀是一家專注於創新藥研發、臨床開發、制造和商業化的生物制藥公司，致力於滿足全球市場尚未滿足的醫療需求。雲頂新耀的管理團隊在中國及全球領先制藥企業擁有深厚的專長和豐富的經驗。公司在浙江嘉善擁有具備商業化規模的全球生產基地，並嚴格按照國家藥品監督管理局（NMPA）和歐洲藥品管理局（EMA）的 GMP 要求及世界衛生組織（WHO）PQ 標准建設。公司聚焦自身免疫、眼科、急重症及CKM（心血管、腎髒及代謝）等疾病治療領域，已打造集全渠道商業化體系與藥品全生命周期商業化能力於一體的商業化平台，並以擁有全球權益的自研 mRNA 平台為基礎，持續推進mRNA in vivo CAR-T 與 mRNA 腫瘤疫苗等現有管線，同時通過引進及生態孵化潛力平台，拓展研發能力，同時強化全球化佈局，加快國際化發展進程。更多信息，請訪問公司官網：www.everestmedicines.com。關於麥科奧特陝西麥科奧特醫藥科技股份有限公司（以下簡稱「麥科奧特」）於2007年1月在西安成立，現已完成西安、蘇州、北京、上海、中國香港、美國佈局。公司是一家專注於新藥研發的創新型醫藥科技企業，致力於成為雙功能和多功能特異性多肽藥物研發的領軍性前沿企業，聚焦於心腦血管、代謝類疾病相關領域的新藥研發。公司是是雙特異性多肽概念的提出者、實施者、驗證者和開發者，是多肽類藥物研發的優秀平台之一，具有篩選多靶點多肽藥物的特殊機制，具備開發First-in-class和Best-in-class品種的平台型研發能力，現已儲備多個新藥品種，其中進入臨床研發的有7個原研創新藥管線，包括1個臨床三期階段，3個臨床二期階段，3個臨床一期階段。公司致力於創制新藥、挽救生命，滿足未被滿足的臨床需求，用科技創新為人類健康保駕護航。更多信息，請訪問公司官網：www.micot.cn。前瞻性聲明本新聞稿所發佈的信息中可能會包含某些前瞻性表述，乃基於本公司或管理層在做出表述時對公司業務運營情況及財務狀況的現有看法、相信、和現有預期，可能會使用「將」、「預期」、「預測」、「期望」、「打算」、「計劃」、「相信」、「預估」、「確信」及其他類似詞語進行表述。這些前瞻性表述並非對未來業績的保證，會受到風險、不確定性及其他因素的影響，有些乃超出本公司的控制範圍，難以預計。因此，受我們的業務、競爭環境、政治、經濟、法律和社會情況的未來變化及發展等各種因素及假設的影響，實際結果可能會與前瞻性表述所含資料有較大差別。本公司及各附屬公司、各位董事、管理人員、顧問及代理未曾且概不承擔更新該稿件所載前瞻性表述以反映在本新聞稿發佈日後最新信息、未來項目或情形的任何義務，除非法律要求。 Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

東京, 2026年2月5日 - (亞太商訊 via SeaPRwire.com) - 專注於產業用貴金屬展開業務的TANAKA PRECIOUS METAL TECHNOLOGIES Co., Ltd.（總公司：東京都中央區，執行總裁：田中 浩一朗）發表在接受委託製造包括體外診斷試劑在內之各種檢驗套組的業務中，確立可一次對應所有製程的綜合式的解決方案體制。迄今為止，TANAKA持續負責的主要是從開發和製造檢驗套組到批量製造萃取液，而此次設置分注及包裝萃取液的生產線，並整建了從開發到製成最終產品可一貫在公司內部完成的體制。藉此得以削減外包與運送所耗費的成本和時間，並可在更短期間內提供高品質產品。另外，預計於2026年3月新增導入最新型的自動組裝產線及萃取液分注設備，旨在進一步擴大生產能力和縮短前置時間。TANAKA綜合式的解決方案體制 透過強化一貫生產體制實現彈性應對透過確立此次綜合式的解決方案體制，從開發和製造檢驗套組到批量製造、分注、包裝萃取液的各個製程已可一貫接受委託。藉此，從客戶的開發階段到量產除了能夠持續支援之外，也可應對僅進行藥劑分注等個別製程的委託。透過在自家公司內部完成的生產製程，進而實現進一步強化穩定供應和品質管理。在廣泛疾病領域中檢驗套組的開發實績與推展實例推出了可應對廣泛傳染病的體外診斷試劑，像是包含流感病毒與新型冠狀病毒等在內的呼吸道傳染病，以及登革病毒與茲卡病毒等。這些檢驗套組已可應對像是唾液、血液及尿液等多種檢體，協助醫療現場進行迅速且準確的診斷。呼吸道傳染病病媒蚊傳染病婦產科・流感病毒・腺病毒・人類呼吸道融合病毒・人類間質肺炎病毒・新型冠狀病毒・A群β型溶血性鏈球菌（鏈球菌）・登革病毒・茲卡病毒・屈公病毒・驗孕試劑TANAKA檢驗目標疾病領域的推展實例技術基礎與今後展望TANAKA自約2006年起開始研究開發體外診斷試劑，並持續培育以金（Au）膠體粒子為核心的技術。擁有多項使用免疫層析法以支援試劑提高性能的技術，像是蛋白質固定化技術、非特異性吸附抑制技術，以及抗原抗體反應增強技術等。而在ISO 13485的認證下，亦運用這些技術接受委託製造高品質檢驗套組。今後將會運用這套綜合式的解決方案體制，也會在與合作夥伴企業進行協作的同時，致力於開發新的診斷試劑，為解決社會課題與推動醫療現場的進步作出貢獻。關於TANAKATANAKA自1885年（明治18年）創業以來，營業範圍以貴金屬為中心，並以此展開廣泛活動。在日本國內，以最高水準的貴金屬交易量為傲的TANAKA，長年以來除了進行產業用貴金屬產品的製造和販售外，並提供資產用與珠寶用的貴金屬商品。本集團以貴金屬專業團隊之姿，旗下的國內外各集團公司協調合作，使製造、販售與技術一體化，並供應相關產品與服務。2024 年度（2024年12月止）的合併營業額為8,469億日圓，擁有5,591名員工。產業事業全球網站https://tanaka-preciousmetals.com產品諮詢表TANAKA PRECIOUS METAL TECHNOLOGIES Co., Ltd.https://tanaka-preciousmetals.com/tw/inquiries-on-industrial-products/新聞媒體諮詢處TANAKA PRECIOUS METAL GROUP Co., Ltd.https://tanaka-preciousmetals.com/tw/inquiries-for-media/新聞稿: https://www.acnnewswire.com/docs/files/20260205_CT.pdf Disclaimer:ANY EXPRESS WRITTEN WARRANTY THAT TANAKA MAY ISSUE, IS THE SOLE AND EXCLUSIVE WARRANTY AS TO TANAKA’S MATERIALS AND PRODUCTS, EXTENDS ONLY TO THE INITIAL PURCHASER FROM TANAKA OR ITS AUTHORIZED DISTRIBUTOR, IS NOT TRANSFERABLE OR ASSIGNABLE, AND IS EXPRESSLY IN LIEU OF AND TANAKA EXPRESSLY DISCLAIMS TO THE EXTENT PERMISSIBLE UNDER APPLICABLE LAW ANY OTHER WARRANTY, ORAL OR IMPLIED, INCLUDING WITHOUT LIMITATION ANY ORAL OR IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR PARTICULAR PURPOSE.TANAKA SHALL NOT BE LIABLE FOR ANY INCIDENTAL, SPECIAL, OR CONSEQUENTIAL LOSS, DAMAGE, OR EXPENSE (INCLUDING, WITHOUT LIMITATION, LOST PROFITS) DIRECTLY OR INDIRECTLY ARISING FROM THE SALE, INABILITY TO SELL, USE, OR LOSS OF USE OF ANY PRODUCT. NO ORAL OR WRITTEN INFORMATION OR ADVICE GIVEN BY TANAKA, ITS EMPLOYEES, DISTRIBUTORS, DEALERS, OR AGENTS SHALL INCREASE THE SCOPE OF ANY WARRANTY OR CREATE ANY NEW WARRANTIES.THE LIMITATIONS AS STATED HEREIN SHALL NOT PRECLUDE ANY LIABILITY WHICH UNDER APPLICABLE PRODUCTS LIABILITY LAW CANNOT LEGALLY BE PRECLUDED BY CONTRACT OR OTHERWISE.NEVER USE THIS TEST KIT AS THE ONLY GUIDE TO MANAGE YOUR CONDITION OR ILLNESS. CONSULT YOUR HEALTHCARE PROVIDER IF YOUR SYMPTOMS PERSIST OR BECOME MORE SEVERE, OR IF YOU ARE CONCERNED AT ANY TIME. Copyright 2026 亞太商訊 via SeaPRwire.com. All rights reserved. www.acnnewswire.com