业聚医疗2025年中期业绩收入及纯利双双增长 分别达8,360万美元及1,980万美元 ACN Newswire

业聚医疗2025年中期业绩收入及纯利双双增长 分别达8,360万美元及1,980万美元

业绩亮点:- 收入达83.6百万美元,同比增长5.9%。- 销量达919,000件,其中779,000件为自有产品,同比增长8.6%。- 公司拥有人应占利润同比上升5.1%至19.8百万美元。- 核心经营利润达15.1百万美元,同比增长11.4%。- 为庆祝集团成立25周年,董事会宣派特别股息每股15港仙。- 财务状况稳健,截至2025年6月30日,现金及银行结余达237.1百万美元,支持潜在收购及新生产设施建设。- 优质产品获全球广泛认可,带动亚太地区市场收入按年增长14.0%,欧洲、中东及非洲市场增长17.0%,及美国市场增长20.0%。- 于上半年收购一家台湾经销商,并计划下半年于比利时及荷兰设立直销团队,进一步加强在亚太地区及欧洲、中东及非洲市场的影响力。- 集团善用全球商业化专长及庞大销售网络,与医疗器械同业建立战略合作,藉此丰富产品组合,并透过交叉销售创造额外收入。香港,2025年8月15日 - (亚太商讯 via SeaPRwire.com) - 专营经皮冠状动脉介入治疗(PCI)及经皮腔内血管成形术(PTA)手术介入器械的全球医疗器械制造公司业聚医疗集团控股有限公司("业聚医疗"或"集团";股份代号:6929)今天宣布截至2025年6月30日止六个月("报告期")的中期业绩。尽管宏观经济环境未见明朗,集团的收入及纯利仍双双录得增长。美国市场增长强劲,加上亚太地区及欧洲、中东与非洲地区新兴市场的持续贡献,推动集团收入达到83.6百万美元,较去年同期上升5.9%。核心经营利润(自本公司拥有人应占利润撇除以股份为基础的薪酬开支、与税务亏损相关的递延税项资产的税务抵免净额及融资收入╱成本)为15.1百万美元,同比增长11.4%。公司拥有人应占利润同比上升5.1%至19.8百万美元。每股基本盈利为2.40美仙(2024年上半年:2.28美仙)。截至2025年6月30日,集团财务状况保持稳健,现金及银行结余达237.1百万美元。鉴于集团的财务状况稳健,以及为庆祝成立25周年,董事会议决宣派特别现金股息每股普通股15港仙,彰显集团致力为股东创造价值。连同截至2024年12月31日止年度之末期股息每股10港仙(已于2025年6月16日派付),股东于2025年合共获派股息每股25港仙。业聚医疗董事长、执行董事兼首席执行官钱永勋先生表示:"过去25年,我们持续投资于创新及全球商业化能力,除了为业聚医疗建立了声誉,也助我们在不同的经济周期中破浪前行。尽管2025年上半年面临宏观经济及地缘政治的双重挑战,我们的全球布局仍展现韧性。美国市场增长印证了市场对我们的优质产品需求殷切,而我们亦透过庞大的销售网络,成功把握了亚太地区及欧洲、非洲及中东地区的增长机遇。我们将继续透过直销市场覆盖、卓越的销售支援、对创新的投入,以及全面的PCI和PTA产品组合提升品牌价值,从而强化竞争优势,为医生及患者提供更安全有效治疗方案的同时,也为股东创造长远回报。"全球销售网络及合作伙伴关系推动收入增长业聚医疗已建立覆盖逾70个国家及地区的销售网络,在13个地区设立直销团队并建立全球经销商网络,成为把握各地机遇、回应当地需求的重要一环。期内,受惠于印尼市场增长,以及Scoreflex TRIO 在新加坡及马来西亚获更广泛采用,亚太地区收入同比上升14.0%至27.3百万美元。欧洲、中东及非洲市场方面,德国、法国及西班牙等直销市场及包括英国、斯洛伐克及捷克共和国在内的分销市场的自有球囊类产品销售表现强劲,带动该区收入上升17.0%至22.4百万美元。尽管受关税因素影响,美国市场收入仍同比上升20.0%至8.0百万美元,主要受冠脉的普通及刻痕球囊,包括高价产品Scoreflex NC球囊,以及外周球囊销量显著上升所推动。而日本及中国境内市场的收入分别为16.1百万美元及9.7百万美元。凭借其广受认可的全球商业化能力,集团与立志走向国际巿场的同业合作,藉此丰富产品组合并开拓额外收入来源。继去年与深圳开立生物医疗科技股份有限公司成功展开合作,在香港及澳门分销血管内超声产品后,集团与该伙伴再度签订独家分销协议,在新加坡及马来西亚分销相关产品。至目前为止,合作范围已进一步扩展至集团旗下位于欧洲的4个直销市场,包括法国、德国、西班牙及瑞士,及其他6个分销市场。性能主导的多元化创新产品组合,提升市场差异化水平截至2025年6月30日,业聚医疗在全球主要司法管辖区拥有逾250项授权专利及已公布专利申请,及逾55款获批产品。期内,集团产品注册及临床试验继续取得进展,包括:- Sapphire 3的美国临床试验进展顺利,预期于2025年第四季度完成病人入组,以支持该产品的FDA纳入CTO适应症,从而与市场上其他传统半顺应性球囊形成差异化;- JADE PLUS及Teleport Glide获得CE标志、Teleport Glide及Scoreflex QUAD获得PMDA批准、COREPASS模组化微导管获得FDA批准、导引导管获得国家药监局批准;- 就Scoreflex TRIO、Sapphire ULTRA、Sapphire NC ULTRA、Sapphire NC 24、JADE PLUS、Teleport XT及Teleport Glide向国家药监局提交注册申请,并就Vascuaid抽吸导管及大管腔延长导管向PMDA提交注册申请。集团拥有庞大的产品管线。在冠状动脉领域,Sapphire PTX紫杉醇药物涂层球囊大约于2025年底在日本展开临床研究;外周方面,JADE Score球囊则预期于2026年向PMDA提交注册申请。合资企业业聚培福在中国境内展开的TricValve临床试验亦取得重大进展,参与医院数量上升,加快了病人入组进度。此外,业聚培福亦正透过"港澳注册药品及医疗器械进入大湾区计划",积极推动大湾区各大医院采用TricValve。TricValve于2025年7月完成首次在中国境内进行的商业化植入手术,达到重要的里程碑。多区域生产基地缓解地缘政治风险截至2025年6月30日,业聚医疗于中国深圳、荷兰荷佛拉肯,以及德国莱茵河畔魏尔设有生产基地,总年产能约为210万件球囊及支架。自2023年底收购eucatech AG以来,集团已投入资源恢复其生产能力,期内产量逐步提升,以供应销售及临床注册所需产品。2025年8月,集团完成位于中国杭州、旗下最大研发及生产基地的主体结构建设,装修工程预期于下半年展开。该基地计划于2027年投产,届时将新增年产能240万件。钱先生总结说:"有见于新兴市场的强劲势头、自研产品陆续成功推出巿场,以及已建立的战略合作,我们对2025年下半年前景保持乐观。除了亚太地区及欧洲、中东及非洲将继续担当主要的增长引擎,我们亦计划将部分市场由分销模式转为直销模式,以强化当地营收能力及市场渗透。欧洲市场将透过于比利时及荷兰设立直销团队加强市场影响力;日本市场则藉新产品上市重拾增长动力;而在中国境内市场,我们则把握政策支持,扩大产品覆盖并加速商业化进程。随着关税争端缓和,美国市场的产品交付亦有望加快。凭借业聚医疗多元化的产品组合、稳健的财务状况及规模经济效益,我们具备优势构建具韧性及竞争力的业务体系,为持份者创造可持续的价值。"关于业聚医疗集团控股有限公司业聚医疗是一家全球医疗器械制造公司,专门生产用于经皮冠状动脉介入治疗(PCI)及经皮腔内血管成形术(PTA)的介入器械。本集团总部位于中国香港,产品销往全球超过70个国家和地区。集团亦积极将业务扩展至结构性心脏病领域。凭借拥有逾20年产品开发经验的内部研发团队,本集团已开发出世界领先的专有技术。如需了解更多详情,请访问集团官网:https://orbusneich.com/ Copyright 2025 亚太商讯 via SeaPRwire.com.
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广发证券荣膺国家数据管理能力成熟度(DCMM)最高等级认证 ACN Newswire

广发证券荣膺国家数据管理能力成熟度(DCMM)最高等级认证

广州,2025年8月15日 - (亚太商讯 via SeaPRwire.com) - 近日,中国电子信息行业联合会公布最新一批获颁数据管理能力成熟度(简称"DCMM")等级证书企业名单,广发证券获评最高等级五级(优化级)认证,成为行业首家获评最高等级的证券公司,标志着公司在数据管理和应用方面达到国内领先水平,为行业数据管理能力建设树立标杆。《数据管理能力成熟度评估模型》(GB/T 36073-2018)是我国数据管理领域正式发布的首个国家标准。该认证从数据战略、数据治理、数据架构、数据应用等多个维度,全面评估企业的数据管理能力。其中,五级(优化级)作为最高等级,标志着企业的数据管理已形成行业最佳实践,具备强大的示范引领作用。一直以来,广发证券高度重视数据管理能力的建设与提升,将数据视为企业核心资产。公司构建了"战略引领、全员参与、跨部门协同、全生命周期管理"的数据管理体系。通过制定清晰的数据战略规划,完善数据治理组织架构与制度流程,强化数据安全与合规管理,持续提升数据质量与应用效能,公司实现了数据管理从"规范"到"优化"的跨越式发展,为业务创新、客户服务升级及风险管理提供了强有力的数据支撑。广发证券副总经理、首席信息官辛治运表示:"公司将以此次获得DCMM五级认证为新的起点,持续深化数据管理能力建设,进一步完善数据治理长效机制,推动数据技术与业务场景的深度融合,并以此为契机,不断提升服务实体经济的质效,为证券行业的数据管理创新与发展贡献更多力量。" Copyright 2025 亚太商讯 via SeaPRwire.com.
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Etrasimod Receives Strong Recommendation in the ACG Clinical Guideline Update: Ulcerative Colitis in Adults for Induction and Maintenance Phase of Moderately to Severely Active UC ACN Newswire

Etrasimod Receives Strong Recommendation in the ACG Clinical Guideline Update: Ulcerative Colitis in Adults for Induction and Maintenance Phase of Moderately to Severely Active UC

HONG KONG, Aug 15, 2025 - (ACN Newswire via SeaPRwire.com) - Everest Medicines today announced that etrasimod (VELSIPITY(R)) has been included in the ACG Clinical Guideline Update: Ulcerative Colitis in Adults (the “Updated Guidelines”). Etrasimod, an S1P receptor modulator, is recommended for the induction of remission in patients with moderately to severely active UC and for continuation in the maintenance of remission, compared with no treatment after induction of remission. Both recommendations are strong, with a moderate quality of evidence.This milestone underscores the high level of recognition from an internationally respected clinical guideline for the therapeutic value of etrasimod and highlights its potential to address the significant unmet medical needs of UC patients, offering a new treatment option worldwide.The updated guidelines were developed by the American College of Gastroenterology (ACG) including the latest evidence from the past five years. They provide a comprehensive summary of new approaches and advances in the treatment and prevention of complications in UC, with the goal of offering clinicians standardized and evidence-based recommendations to better manage patients with varying degrees of disease severity.The updated guidelines note that, etrasimod is an oral, once-daily, selective sphingosine 1-phosphate (S1P) 1,4,5 receptor modulator for the treatment of moderately to severely active UC. The S1P 1 receptor modulation regulates the trafficking of specific lymphocyte subsets out of the lymph nodes, leaving fewer peripheral immune cells available to traffic to sites of inflammation.The updated guidelines also reference the Phase III ELEVATE UC clinical study for etrasimod (ELEVATE UC 52 and ELEVATE UC 12). Both studies achieved all primary and key secondary efficacy endpoints, with a favorable safety profile consistent with previous studies of etrasimod. Etrasimod has been included in the AGA Living Clinical Practice Guideline on the pharmacological management of moderate-to-severe UC as one of the higher-efficacy medications suggested for first-line use in advanced therapy-naïve patients.Prof. Wu Kaichun at the First Affiliated Hospital of AFMU who is the principal investigator for etrasimod’s Asia clinical trial said “The updated guidelines further emphasize that achieving endoscopic mucosal healing to enable sustained, steroid-free remission is a core treatment goal for patients. This is not only critical for the long-term and safe management of the disease but is also closely tied to improving patients’ quality of life. The strong recommendation of etrasimod for both induction and maintenance therapy in this population reflects the high level of recognition from an internationally authoritative medical authority.”“The inclusion of etrasimod in the 2025 American College of Gastroenterology (ACG) Clinical Guideline for Adult Ulcerative Colitis, with a strong recommendation, is a clear recognition of its clinical efficacy and favorable safety profile. Mucosal healing is a recognized treatment goal in both domestic and international clinical guidelines for UC. Achieving mucosal healing at an early stage can significantly reduce the risk of disease relapse, hospitalization, colectomy, and the development of colorectal cancer.” said Rogers Yongqing Luo, Chief Executive Officer of Everest Medicines. “In Asia, the number of UC patients continues to rise, while treatment options remain limited, highlighting an urgent need for innovative therapies that balance efficacy, safety, and convenience. In China alone, the UC patient population was estimated at approximately 800,000 in 2024 and is projected to reach 1 million by 2030, placing an increasing burden on the healthcare system.”As a key innovative asset in Everest Medicines’ autoimmune disease portfolio, etrasimod’s inclusion in the clinical guidelines underscores its global therapeutic potential as a new treatment option for UC patients across Asia, including in China. We remain committed to accelerating the regulatory approval process for etrasimod in Mainland China, South Korea, and other Asian markets to enhance patient access and help more individuals achieve higher-quality, longer-lasting disease remission.”As a core product of Everest Medicines, etrasimod has been approved in Singapore, Macao SAR, and Hong Kong SAR, and its NDA has been accepted in South Korea. In December 2024, China’s National Medical Products Administration (NMPA) officially accepted the NDA for VELSIPITY(R). As Everest’s third commercialized product, VELSIPITY(R) has been officially approved by the Guangdong Provincial Medical Products Administration for adult patients with moderately to severely active UC. It is now available at medical institutions designated under the Connect Policy in the Greater Bay Area. Additionally, Everest has launched a factory construction project at its Jiashan site to support local production of VELSIPITY(R). Copyright 2025 ACN Newswire via SeaPRwire.com.
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OrbusNeich Records Growth in 2025 Interim Results, Revenue and Net Profit Reach US$83.6 Million and US$19.8 Million Respectively ACN Newswire

OrbusNeich Records Growth in 2025 Interim Results, Revenue and Net Profit Reach US$83.6 Million and US$19.8 Million Respectively

Results Highlights:- Revenue reached US$83.6 million, a year-on-year increase of 5.9%.- Sales volume reached 919,000 units, of which 779,000 units were proprietary products, representing a year-on-year increase of 8.6%.- Profit attributable to owners of the company increased by 5.1% year-on-year to US$19.8 million.- Core operating profit amounted to US$15.1 million, an increase of 11.4% year-on-year.- The Board declared a special dividend of HK15 cents per share to mark the Group’s 25th anniversary.- The Group maintained a sound financial position with cash and bank balances of US$237.1 million as of June 30, 2025 to support potential acquisitions and the construction of new manufacturing facilities.- The Group’s high-quality products have gained widespread recognition worldwide, resulting in revenue growth of 14.0% in the APAC market, 17.0% in the EMEA market, and 20.0% in the US market.- The Group acquired a Taiwan-based distributor in the first half of the year. It also plans to establish direct sales teams in Belgium and the Netherlands in the second half of the year, further strengthening direct presence in APAC and EMEA markets.- Leveraging its global commercialization expertise and extensive distribution network, the Group established strategic partnerships with medical device peers, thereby diversifying its product portfolio and generating additional revenue through cross-selling opportunities.HONG KONG, Aug 15, 2025 - (ACN Newswire via SeaPRwire.com) - OrbusNeich Medical Group Holdings Limited (“OrbusNeich” or the “Group”; stock code: 6929), a multinational medical device company specializing in interventional devices for percutaneous coronary intervention (“PCI”) and percutaneous transluminal angioplasty (“PTA”) procedures, today announced its interim results for the six months ended June 30, 2025 (the “Period”), reporting growth in both revenue and net profit despite an uncertain macroeconomic landscape.The Group recorded revenue of US$83.6 million, up 5.9% over the previous year, driven by strong year-on-year growth in the US market, as well as continued contributions from emerging markets in APAC and EMEA. Core operating profit, being profit attributable to the owners of the Company excluding share-based compensation, net tax credit from deferred tax asset in relation to tax losses, and finance income/costs, amounted to US$15.1 million, up by 11.4% year-on-year. Profit attributable to the owners of the Company increased by 5.1% year-on-year to US$19.8 million. Basic earnings per share was US2.40 cents (first half of 2024: US2.28 cents).As of June 30, 2025, the Group maintained a strong financial position with cash and bank balances amounting to US$237.1 million. In light of the Group’s solid financial position and in celebration of the its 25th anniversary, the Board has resolved to declare a special dividend of HK15 cents per ordinary share, demonstrating the Group’s commitment to creating value for its Shareholders. Together with the final dividend of HK10 cents per share for the year ended December 31, 2024 paid on June 16, 2025, Shareholders will receive a total dividend of HK25 cents in 2025.Mr. David Chien, Chairman, Executive Director and Chief Executive Officer of OrbusNeich, said, “Over the past 25 years, we have continuously invested in innovation and global commercial capabilities, establishing OrbusNeich’s reputation and enabling us to navigate different economic cycles. Despite macroeconomic and geopolitical challenges in the first half of 2025, our global deployment proved resilient. Growth in the US market reflected strong demand for our high-quality products, while our extensive sales network successfully captured growth opportunities in the APAC and EMEA regions. We will continue to sharpen our competitive edge by enhancing brand value through our direct sales market presence, excellent sales support, commitment to innovation, and comprehensive PCI and PTA product portfolio, while advancing safer, more effective solutions for physicians and patients and delivering long-term returns to shareholders.”Global Sales Network and Partnerships Boost Revenue GrowthOrbusNeich has built a sales network spanning over 70 countries and regions, including direct teams in 13 locations and a global distributor network, which proven integral to capturing local opportunities and demand worldwide. APAC revenue rose by 14.0% year-on-year to US$27.3 million during the Period, fueled by growth in Indonesia and increasing adoption of Scoreflex TRIO in Singapore and Malaysia. EMEA revenue grew 17.0% to US$22.4 million, driven by strong proprietary balloon product sales in key direct markets (Germany, France, Spain) and distributor markets (the UK, Slovakia, Czech Republic). Despite tariff disruptions, US revenue increased by 20.0% to US$8.0 million, boosted by a notable surge in sales volume of standard and scoring coronary balloons and peripheral balloons, including the high-priced Scoreflex NC balloon. Revenue from the Japan and PRC markets was US$16.1 million and US$9.7 million, respectively.Leveraging its widely-recognized global commercialization expertise, the Group partnered with peers pursuing international expansion to enrich its product portfolio and drive additional revenue streams. Building on the successful collaboration with SonoScape Medical Corp. involving the distribution of intravascular ultrasound (“IVUS”) products in Hong Kong and Macau last year, the Group has entered into a sole and exclusive distribution agreement with this partner to distribute its IVUS products in Singapore and Malaysia. The collaboration now covers four additional direct European markets (France, Germany, Spain, Switzerland) and six other distributor markets across Europe.Performance-Led Innovation Fuels Market Distinction and Portfolio DiversityAs of June 30, 2025, OrbusNeich had obtained more than 250 granted patents and published patent applications in key jurisdictions worldwide, as well as over 55 approved products.During the Period, the Group made progress in terms of product registrations and clinical trials, including:- Sapphire 3’s US trial progressing smoothly, with patient enrollment set to finish in Q4 2025 to support FDA submission for the CTO indication, distinguishing it from other conventional semi-compliant balloons on the market;- Obtained CE Marks for JADE PLUS and Teleport Glide, PMDA approvals for Teleport Glide and Scoreflex QUAD, FDA approvals for the COREPASS Modular Microcatheter, and NMPA approval for the guiding catheter;- Submitted registration applications for Scoreflex TRIO, Sapphire ULTRA, Sapphire NC ULTRA, Sapphire NC 24, JADE PLUS, Teleport XT and Teleport Glide to the NMPA, and applications for the Vascuaid Aspiration Catheter and GCE Large Lumen to the PMDA.Regarding the Group’s robust product pipeline, the Sapphire PTX paclitaxel drug-coated balloon, in the coronary space, is set to begin clinical trials in Japan near the end of 2025. In the peripheral space, the JADE Score balloon is expected to be submitted for PMDA approval in 2026.The joint venture OrbusNeich P&F also made significant progress in the clinical trials of TricValve in the PRC, with the number of participating sites increased to accelerate patient enrollment. In addition, it has been actively promoting TricValve’s entry into hospitals in the Greater Bay Area (“GBA”) through the Hong Kong & Macau Registered Drugs and Medical Devices Access to GBA Program. The first commercial implantation of TricValve in the Mainland of China was completed in July 2025, marking the achievement of an important milestone.Multi-Region Production Bases Mitigate Evolving Geopolitical RisksAs of June 30, 2025, OrbusNeich’s aggregate annual production capacity was approximately 2.1 million balloons and stents, with production facilities in Shenzhen, the PRC; Hoevelaken, the Netherlands; and Weil am Rhein, Germany. Since acquiring eucatech AG in late 2023, the Group has allocated resources to restore its production capabilities, gradually ramping up output during the Period to supply products for both sales and clinical registries.The Group completed the main structure construction of its largest R&D and production facility in Hangzhou, the PRC, in August 2025, with renovation work expected to begin in the second half of the year. The facility is scheduled to commence operations in 2027, adding an annual production capacity of 2.4 million units.Mr. Chien concluded, “We remain optimistic about the second half of 2025 due to strong momentum in emerging markets, successful proprietary product launches, and strategic partnerships. APAC and EMEA will remain our key growth drivers, with plans to transition selected markets from distributor to direct sales models to enhance revenue and market presence. In Europe, we will establish direct sales teams in Belgium and the Netherlands to expand our footprint. The Japanese market will see renewed momentum through new product launches, while in the PRC market, we will capitalize on policy support to expand product coverage and accelerate commercialization. US shipments are expected to speed up amid easing tariff disputes. Backed by OrbusNeich’s diversified portfolio, strong financial position, and economies of scale, we are well positioned to build a resilient, competitive business that delivers sustainable value to stakeholders.”About OrbusNeich Medical Group Holdings LimitedOrbusNeich is a multinational medical device company specializing in interventional devices for percutaneous coronary intervention (PCI) and percutaneous transluminal angioplasty (PTA) procedures. Headquartered in Hong Kong, China, our Group sells its products in more than 70 countries and regions worldwide. It is also actively expanding into structural heart disease. With an in-house R&D team boasting over 20 years of product development expertise, our Group has developed world-leading proprietary technologies.For more information, please visit the Group’s official website: https://orbusneich.com/. Copyright 2025 ACN Newswire via SeaPRwire.com.
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RAK ICC Strengthens Foundations Regime with 2025 Legislative Enhancements ACN Newswire

RAK ICC Strengthens Foundations Regime with 2025 Legislative Enhancements

RAS AL KHAIMAH CITY, UAE, Aug 14, 2025 - (ACN Newswire via SeaPRwire.com) - Ras Al Khaimah International Corporate Centre (RAK ICC) has announced significant amendments to its Foundations Regulations 2019, which took effect on 31 July 2025. The changes represent one of the most substantial updates to the regime since its introduction, reinforcing the UAE's position as a competitive jurisdiction for wealth structuring and long-term asset protection.RAK ICC Foundations are widely recognized for their flexibility, confidentiality, and legal robustness, making them a preferred choice for high-net-worth individuals, entrepreneurs, and family offices, both within the UAE and internationally. These structures are commonly used for succession planning, family governance, and consolidating diverse assets under a single legal entity.The 2025 amendments introduce stronger legal safeguards and improved governance measures which include:Firewall Provisions - Stronger protection from foreign judgments conflicting with RAK ICC Regulations.Three-Year Statute of Limitations - Limits challenges to establishment or asset transfers to three years.Cause of Action Provisions - Creditor fraud claims are limited to the specific asset involved and only if rendering the founder insolvent.Duress and Officer Protections - Nullifies actions taken under foreign legal coercion, preserving internal governance autonomy of a foundation.Strengthened Arbitration Framework - Disputes can be resolved privately with court-level powers.Private Trustee Foundation Provisions - Clarifies asset segregation and fiduciary integrity for property held in trust by a foundation.Assets held within RAK ICC Foundation will now benefit from enhanced firewall provisions, ensuring that foreign judgments conflicting with UAE law cannot be enforced against them. A new three-year limitation period has been established for challenging the formation of a foundation or the transfer of assets into it, providing greater certainty for founders and beneficiaries. The reforms also tighten creditor protection rules by requiring proof of insolvency in fraudulent transfer claims, with liability capped at the value of the disputed asset to prevent overreach into unrelated holdings.In addition, the updated regulations address governance integrity and operational resilience. Officers of a foundation who receive foreign orders inconsistent with RAK ICC law are obligated to disregard them, thereby safeguarding the autonomy of the foundation's decision-making. The framework now explicitly confirms that assets held in trust by a foundation are legally distinct and separate from foundation property, ensuring clear asset segregation. Dispute resolution has also been strengthened, with arbitration provisions expanded to grant tribunals court-like powers, enabling disputes to be resolved efficiently, confidentially, and in line with international best practices.These changes are part of RAK ICC's broader strategy to maintain a forward-looking legal and regulatory environment that meets global standards while catering to the specific needs of its client base. They reflect the jurisdiction's commitment to supporting sophisticated wealth planning strategies that balance control, privacy, and long-term security.By enhancing its Foundations regime, RAK ICC is cementing its position in the UAE as a trusted partner for those seeking secure, adaptable, and internationally compliant solutions for wealth preservation and intergenerational planning.About RAK ICCRas Al Khaimah International Corporate Centre (RAK ICC) is a corporate registry based in Ras Al Khaimah, United Arab Emirates. The organisation provides international business companies and foundations, typically used for private and business structuring, asset consolidation, and succession planning. To date, RAK ICC has incorporated thousands of international companies and supports multi-billion dirhams in structured assets. It serves high-net-worth individuals, entrepreneurs, and businesses seeking flexible and secure solutions for long-term business and wealth management.For media enquiries, contact us at:Phone: +971 7 207 7177Email: info@rakicc.comWebsite: https://www.rakicc.com/contact-us/SOURCE: RAK ICC Copyright 2025 ACN Newswire via SeaPRwire.com.
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MMG Announces 2025 Interim Results, Profit, Earnings and Cash up on Strong Copper Growth ACN Newswire

MMG Announces 2025 Interim Results, Profit, Earnings and Cash up on Strong Copper Growth

HONG KONG, Aug 12, 2025 - (ACN Newswire via SeaPRwire.com) - MMG Limited (“MMG”, stock code: 1208) has today announced its Interim Results with a net profit after tax of US$566.3 million. This represents more than a 600 per cent increase compared to a net profit after tax of US$79.5 million in the first half of 2024.The strong profit growth was primarily driven by increased copper production across all three copper mines, higher market prices for copper, gold, silver and zinc, as well as reduced unit costs at Las Bambas driven by higher copper production.“Over the first half of the year, our business delivered an outstanding operational and financial performance,” said Ivo Zhao, MMG’s CEO. “This result reflects the strength of our portfolio, the capability of our people, and the disciplined execution of our strategy.”Importantly, MMG’s safety performance improved with a total recordable injury frequency (TRIF) of 1.81 per million hours worked in the first half of 2025, an improvement compared to the full-year 2024 TRIF of 2.06. The significant events with energy exchange frequency (SEEEF) for the first half of 2025 remained consistent with the 2024 figure at 0.78 per million hours worked.Operationally, MMG achieved impressive copper sales and significantly improved production across all three of its copper assets, including a strong performance from Las Bambas and the ramp-up at Khoemacau and Kinsevere. Its Australian operations also maintained solid zinc production, despite navigating challenges including weather impacts, equipment reliability and lower grades due to mining sequence.Highlights include:Record first-half results for both EBITDA and EBIT, with EBITDA at US$1,539.9 million, representing a 98 per cent increase compared to the first half of 2024, and EBIT totalling US$1,058.8 million, an increase of 240 per cent over the same period.Net profit after tax was US$566.3 million, including a profit of US$340.0 million attributable to equity holders of the company.A 130 per cent increase in net cash flow from operations, totalling US$1,185.0 million, compared to the first half of 2024. This performance was mainly driven by increased copper sales and higher commodity prices.Balance sheet improvements, with record lows - since the acquisition of Las Bambas - in both net debt and gearing ratio. The Company’s net debt declined by US$903.3 million since the end of 2024, attributed to robust operational cash flow and the early repayment of US$500 million in Khoemacau Joint Venture Group borrowings. Gearing reduced from 41 per cent to 33 per cent over the first half of 2025.Record high total payable copper sales since 2018, reaching 237,651 tonnes in the first half of 2025.Las Bambas produced 210,637 tonnes of copper in copper concentrate in the first half of 2025, marking a 67 per cent increase compared to the same period in 2024. EBITDA reached a record high of US$1,310.5 million, representing a 122 per cent increase compared to the first half of 2024.“MMG’s balance sheet is in great shape – its strongest in 10 years - with debt reduction driven by higher profits and cash generation,” continued Mr Zhao. “Our ambition to become a top 10 global copper producer is within reach and we are well-positioned to achieve this through operational excellence, disciplined capital allocation, and a continued commitment to responsible mining.”Guidance for the year remains unchanged with total production aiming for a high end of 522,000 tonnes of copper and 240,000 tonnes of zinc. Las Bambas is expected to produce up to 400,000 tonnes of copper this year, assuming stable operating conditions and limited external disruptions. MMG is focussed on delivering its cost targets, with Las Bambas and Rosebery favourably adjusting their C1 cost range to reflect improved by-product credits and strong market conditions.The company is working to complete the recent Nickel Brazil acquisition and is confident in the long-term portfolio and growth contribution. MMG remains committed to supporting community development, strong local economies and employment and supplying the critical minerals the world needs for a sustainable future.Read the 2025 Interim Results announcement, watch a short CEO message and download company photos.About MMG Founded in 2009, MMG’s vision is to create a leading international mining company for a low carbon future. The company is headquartered in Melbourne, Australia and Beijing, China and listed on the Hong Kong Stock Exchange (HKEX1208). MMG’s portfolio supports copper, zinc and cobalt production, with soon to be nickel – products that are critical to achieving global decarbonisation and electrification targets. With operations in Australia, Botswana, the Democratic Republic of Congo and Latin America. More info here. Copyright 2025 ACN Newswire via SeaPRwire.com.
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Formerra Becomes North American Distributor for Syensqo PVDF ACN Newswire

Formerra Becomes North American Distributor for Syensqo PVDF

ROMEOVILLE, IL, Aug 12, 2025 - (ACN Newswire via SeaPRwire.com) - Formerra, a leader in performance materials distribution, has signed an agreement with Syensqo to distribute its Solef® Polyvinylidene Fluoride (PVDF) materials in North America. The agreement expands access to this critical material known for its combination of chemical resistance and flexibility. Solef® PVDF joins a growing list of high-performance materials in Formerra's portfolio designed to advance product development and innovation."With this new agreement, Formerra will be able to support customers across multiple markets with the materials they need to meet demanding application requirements," said Bob Long, Business Development Manager at Formerra. "In addition, this reinforces our commitment to delivering unmatched access, application support, and advanced materials for customers navigating complex performance and regulatory challenges."PVDF is positioned near the top of the performance pyramid for its outstanding chemical and heat resistance. Its inherent flexibility further enhances its suitability for demanding applications in chemical processing, healthcare, and automotive industries. Key properties* include:Heat resistance: Continuous use temperatures up to 150 degrees C (302 degrees F), bursting pressures of up to 139 bar (2,017 psi) at room temperatureChemical purity: Ultra-pure water resistivity, meeting SEMI F-57 specifications for the semiconductor industryBalance of strength and flexibility: Tensile yield strength up to 55 MPa (8,000 psi) with elongation at break up to 100%"We chose Formerra as our distribution partner for Solef® PVDF in North America because of their technical and commercial reach," said Rose Catherin, Sales Director Americas, Channel partners, Distribution and Digital Sales at Syensqo Specialty Polymers. "Their commitment to excellence and long-standing presence in critical markets make them an ideal fit to help expand the availability and use of Solef® PVDF."*As measured by TDSCaption: Formerra Becomes North American Distributor for Syensqo Solef®PVDF.Key Details:Formerra is an authorized distributor of Solef® PVDF from Syensqo in North America.The agreement includes support for high-performance applications across a broad spectrum of industries.PVDF offers excellent chemical resistance, thermal stability, and flexibility.Formerra provides technical guidance and supply chain expertise to support material selection and application development.About FormerraFormerra is a preeminent distributor of engineered materials, connecting the world's leading polymer producers with thousands of OEMs and brand owners across healthcare, consumer, industrial, and mobility markets. Powered by technical and commercial expertise, it brings a distinctive combination of portfolio depth, supply chain strength, industry knowledge, service, leading e-commerce capabilities, and ingenuity. The experienced Formerra team helps customers across multiple industries to design, select, process, and develop products in new and better ways - driving improved performance, productivity, reliability, and sustainability. To learn more, visit www.formerra.com.Media ContactJackie MorrisMarketing Communications Manager, Formerrajackie.morris@formerra.com+1 630-972-3144SOURCE: Formerra Copyright 2025 ACN Newswire via SeaPRwire.com.
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Cryofocus Medtech Achieves Record Interim Results with 162% Revenue Surge Driven by Respiratory Intervention Products ACN Newswire

Cryofocus Medtech Achieves Record Interim Results with 162% Revenue Surge Driven by Respiratory Intervention Products

HONG KONG, Aug 11, 2025 - (ACN Newswire via SeaPRwire.com) - Cryofocus Medtech (Shanghai) Co., Ltd. ("Cryofocus" or the "Company," Stock Code: 6922.HK), a global innovator in minimally invasive interventional cryotherapy, last friday announced its unaudited interim results for the six months ended June 30, 2025. The Company demonstrated robust growth momentum and significant operational optimization during the reporting period, with key financial metrics delivering exceptional performance. Notably, its respiratory intervention product portfolio fueled a substantial revenue surge, marking accelerated commercialization progress.Respiratory Intervention Products Emerge as Core Growth Engine, Highlighting Global Competitive EdgeThe Company recorded revenue of RMB51.1 million for the first half of 2025, a 162.4% increase from RMB19.5 million in the same period of 2024, setting a new historical high. This growth was primarily attributable to the strategic focus on respiratory intervention products entering a harvest phase: The Malignant Stenosis Cryoablation System, approved by China’s National Medical Products Administration (NMPA) in March 2025, and the previously commercialized Cryoadhesion System, experienced rapid sales expansion, becoming the dominant revenue drivers. Additionally, the distribution partnership with Boston Scientific’s China affiliate, BSC International Medical Trading (Shanghai) Co., Ltd. (“BSC”), contributed significant incremental revenue from other respiratory intervention products in mainland China.Of particular significance, the Company’s Asthma Cryoablation System received "Breakthrough Medical Device" designation from the U.S. Food and Drug Administration (FDA) – the first such international recognition for a Chinese enterprise in the respiratory interventional cryotherapy field – laying a foundation for global market expansion.Cryofocus has established a highly competitive respiratory intervention portfolio addressing critical indications, including malignant stenosis, benign stenosis, asthma, chronic obstructive pulmonary disease (COPD), peri-pulmonary nodules, chronic cough, and airway tuberculosis. Among these: The Malignant Stenosis Cryoablation System has been successfully commercialized in China; systems for asthma and COPD are in confirmatory clinical trials with expected approvals in 2026; products for cough, tuberculosis, and peri-pulmonary nodules are in various R&D stages; and the Cryoadhesion System (including disposable and re-sterilizable cryoprobes) is approved and marketed. These innovations mainly stem from Cryofocus’s two core technology platforms: unique liquid nitrogen-based cryoablation technology (utilizing liquid nitrogen as the cryogenic energy source) and advanced flexible catheter technology. This integrated platform enables deep low-temperature treatment, precise control, and minimally invasive intervention, offering superior therapeutic efficacy and safety while creating significant technological barriers for competitors.Platform Value Multiplies as Multi-Segment Strategy Accelerates CommercializationCryofocus’s core value extends beyond its respiratory pipeline, underpinned by its distinction as an innovative cryotherapy platform enterprise. Leveraging its liquid nitrogen and flexible catheter technologies, the Company has successfully expanded into multiple high-potential therapeutic areas:In the vascular intervention segment: The Atrial Fibrillation (AF) Cryoablation System (for atrial fibrillation treatment) was commercialized in China in September 2024. The Cryofocus Renal Denervation (Cryo-RDN) System (for hypertension treatment), granted FDA Breakthrough Device designation, is in confirmatory clinical trials. The Pulmonary Hypertension Cryoablation System is currently in the stage of pre-clinical study. The market space for all these related cardiovascular indications is very huge.In the Natural Orifice Transluminal Endoscopic Surgery (NOTES) segment: The respiratory intervention portfolio, as detailed, is rich and leading. The cancer intervention portfolio includes the commercialized Bladder Cryoablation System; the Gastric Cryoablation System and Esophageal Cryospray System are in clinical trials targeting gastric and esophageal cancer markets.In non-cryotherapy products: Commercialized items such as the Pulmonary Nodule Localization Needle and Endoscopic Clip for Anastomosis, alongside pipeline products like the Atrial Fibrillation Pulsed Field Ablation (PFA) System and Anti-Gastroesophageal Reflux System, create complementary synergies.This "one-platform, multi-therapy" model endows Cryofocus with exceptional adaptability for indication expansion and pipeline sustainability. The Company currently boasts a robust portfolio of 23 products and candidates: 14 cryotherapy and 9 non-cryotherapy items, with 11 already commercialized. Such platform-based diversification is rare among single-therapy medical device firms, highlighting substantial long-term growth potential and risk resilience.Strong Financial Performance and Sustained Growth MomentumBeyond the revenue surge driven by respiratory products, Cryofocus’s interim results signal positive ongoing growth. The Company’s technological advantages further translated into financial resilience. Gross profit reached RMB34.3 million for the first half of 2025, up 124.5% year-on-year, with a solid gross profit margin of 67.1%. Enhanced R&D efficiency led to significantly reduced losses. R&D expenses optimized to RMB17.9 million (down 51.9% year-on-year), while the period loss narrowed 51.4% to RMB27.2 million, demonstrating a clear trend toward profitability. Cash reserves increased 40.1% from year-end 2024 to RMB63.7 million, providing a solid foundation for sustained R&D and market expansion.Revenue diversification and quality improved as high-value self-developed products (e.g., Malignant Stenosis Cryoablation System) launched and scaled, complemented by deepening collaboration with BSC. The significant reduction in R&D expenses reflects improved efficiency and reduced consumable needs as products advance, driven by optimized personnel costs and management enhancements. This establishes a sound framework for balancing innovation intensity with cost control.Furthermore, the Company increased investment in sales network development, with selling and distribution expenses rising 174.4% year-on-year to RMB9.2 million, underscoring proactive resource allocation to build marketing teams and promote newly launched products (e.g., Malignant Stenosis Cryoablation System), laying groundwork for future sales scale expansion.Global Peer Benchmark Highlights Valuation PotentialCryofocus’s technological strength in respiratory interventional cryotherapy, particularly in FDA-designated areas like asthma treatment, positions it competitively against global leaders.Benchmarked against Inspire Medical Systems (INSP) (focusing on OSA neurostimulation, differing in indication but similar in respiratory neuro-intervention): Inspire currently holds a market capitalization of US$2.279 billion and a trailing-twelve-month (TTM) P/E ratio of 44.28x. Cryofocus’s Asthma Cryoablation System similarly targets pulmonary vagal nerves via minimally invasive ablation, with an innovative pathway validated by FDA Breakthrough status. Yet, as a diversified platform innovator with a broad pipeline and multiple commercialized products, Cryofocus’s current Hong Kong market valuation (Inspire’s market cap is 12.8x Cryofocus’s) significantly trails Inspire’s.This substantial valuation gap, while influenced by factors such as differing markets (US vs. HK), stages of development (Inspire being profitable and established in the US market), and a single-product focus versus a platform model, nonetheless clearly underscores the significant upside potential in Cryofocus Medtech's current market valuation relative to its technological capabilities, the breadth of its product pipeline, and its potential for globalization breakthroughs. With the advancement of clinical progress for its respiratory intervention products (particularly the Asthma Cryoablation System COPD Cryospray System Peri-Pulmonary Nodule Cryoablation System), the clarification of overseas registration pathways, and the continued high-speed growth in its revenue scale, a market re-rating of its value represents a high-probability event. The current valuation level presents an attractive window of opportunity for investors bullish on the long-term prospects of the minimally-invasive interventional cryotherapy sector and the value inherent in a platform company model.Looking ahead, Cryofocus maintains a clear strategy: rapidly advance clinical development and commercialization of pipeline products; deepen focus on minimally invasive interventional cryotherapy while expanding the portfolio leveraging its core platforms; continuously invest in underlying and supporting technologies; and selectively expand global operations. The Company is steadily transitioning from R&D-driven to a dual-engine model integrating R&D and commercialization, advancing resolutely toward its vision of becoming a "global platform for minimally invasive interventional cryotherapy medical devices." Copyright 2025 ACN Newswire via SeaPRwire.com.
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How Do AI Workflow Automations Work? ACN Newswire

How Do AI Workflow Automations Work?

SINGAPORE, Aug 16, 2025 - (ACN Newswire via SeaPRwire.com) - A 2022 survey from Vanson Bourne revealed that around 91%1 of respondents saw increased demand for automation from business teams. As AI technology evolves, that demand will only grow. AI automations can help organizations work smarter at every level. But how exactly do these workflows function? This article unpacks what AI workflow automation is and how it works behind the scenes.What is AI workflow automation?AI workflow automation is the use of artificial intelligence to automate complex, multi-step tasks that typically require human decision-making. While rule-based automation may rely on rigid instructions, AI automation adapts to data patterns. It learns over time and can flexibly handle unstructured input like emails, documents, or customer requests.AI workflow tools can understand, decide, and act based on context. These tools can help streamline processes and reduce manual effort while improving speed and accuracy.How do AI workflows function?AI workflows function by connecting a series of intelligent tasks or steps to complete a goal from start to finish. The specific tasks can vary depending on the use case. Some workflows may be entirely automated, while some may require human input. Let's take a closer look at some core components that power AI workflows.Machine learning (ML)Machine learning models can make predictions, identify problems, or find patterns. Machine learning has many uses in a workflow including classifying documents or prioritizing tasks. ML acts as the "decision engine", helping automate steps that would otherwise require manual analysis or classification.Natural language processing (NLP)NLP allows AI systems to understand and interpret human language for seamless communication. It's a crucial component in workflows that involve text, speech, or communication. For example, NLP can automatically extract key data from emails or summarize meeting notes. This enables organizations to automate content-heavy tasks without sacrificing understanding or context.Automation triggersAI workflows are usually event-driven. A trigger might be a form submission, a task status update, or an incoming message. Once initiated, the AI workflow executes a sequence of tasks based on logic, conditions, and model predictions. These triggers help organizations respond faster, reduce delays, and eliminate manual intervention.Predictive algorithmsPredictive AI models help forecast future outcomes based on past behavior. These algorithms can be used to detect workflow bottlenecks or even predict them based on past occurrences. Effective predictive models require good data and smart integration. When done right, they can help businesses make smarter, data-informed decisions with minimal human input.Benefits of AI workflowsHere are some of the advantages that AI workflows offer.Increased efficiency: Automations can take on repetitive and time-consuming tasks. This frees up teams to focus on more strategic work.Scalability: AI workflows can process large volumes of data or requests without extra headcount. They make it easier to scale services or operations.Improved accuracy: Trained models and rule-based logic may help reduce the risk of human error.Faster decision-making: AI workflows can analyze data and trigger decisions in real time. This may enable businesses to respond to problems or opportunities faster.From streamlining internal operations to powering real-time customer experiences, AI workflow automation is helping businesses scale their operations at a reduced cost. AI workflows offer a powerful path toward enhanced efficiency.[1] Vanson Bourne - Case studies Salesforce Business Demand for Automation. June 2022. https://www.vansonbourne.com/case-studies/business-demand-for-automation/CONTACT:Sonakshi MurzeManagersonakshi.murze@iquanti.comSOURCE: iQuanti Copyright 2025 ACN Newswire via SeaPRwire.com.
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Everest Medicines’ New Drug Application for Etrasimod Accepted in Taiwan, Marking Another Milestone in Asia Market Access ACN Newswire

Everest Medicines’ New Drug Application for Etrasimod Accepted in Taiwan, Marking Another Milestone in Asia Market Access

HONG KONG, Aug 14, 2025 - (ACN Newswire via SeaPRwire.com) - Everest Medicines (HKEX 1952.HK, “Everest”) today announced that the Taiwan Food and Drug Administration (TFDA) has officially accepted the New Drug Application (NDA) for VELSIPITY(R) (etrasimod) for the treatment of patients with moderately to severely active ulcerative colitis (UC).Building on prior approvals in Singapore, Hong Kong SAR, and Macao SAR, as well as NDA acceptance in South Korea, this marks significant progress in the commercialization of VELSIPITY(R) across Asia. In December 2024, China’s National Medical Products Administration (NMPA) officially accepted the NDA for VELSIPITY(R).As a next-generation selective S1P receptor modulator, once-daily oral etrasimod demonstrates robust efficacy across multiple endpoints, including clinical remission, mucosal healing, endoscopic normalization and histological remission. Its clinical value has been robustly demonstrated in multiple global Phase III studies, including ELEVATE UC 52, ELEVATE UC 12 and ENLIGHT (ES101002) studies.“The NDA acceptance for VELSIPITY(R) in Taiwan, China marks another key progress in our commercialization pathway across Asia. As the number of UC patients in Asia continues to rise, there remains a significant unmet medical need. In China alone, there were approximately 800,000 patients with UC in 2024, and the number is estimated to reach 1 million by 2030. UC patients face the dual challenges of long-term treatment and maintaining quality of life." said Rogers Yongqing Luo, Chief Executive Officer of Everest Medicines. “This NDA acceptance underscores the clinical value of VELSIPITY(R). We remain committed to accelerating access to this innovative therapy in Mainland China and other Asian markets, supporting long-term disease management while enhancing patients’ quality of life.”The clinical part submitted to TFDA is mainly based on results from the ELEVATE UC Phase 3 registrational program (ELEVATE UC 52 and ELEVATE UC 12) and the ENLIGHT study (ES101002). The ELEVATE UC Phase 3 registrational program evaluated the safety and efficacy of etrasimod 2 mg once-daily on clinical remission in UC patients with moderately to severely active UC who had previously failed or were intolerant to at least one conventional, biologic, or Janus kinase (JAK) inhibitor therapy. Both studies achieved all primary and key secondary efficacy endpoints, with a favorable safety profile consistent with previous studies of etrasimod.The ENLIGHT study (ES101002) conducted by Everest, is a multicenter, randomized, double-blind and placebo-controlled Phase 3 trial of etrasimod in Asian countries, including China Mainland, China Taiwan and South Korea. This is the largest Phase 3 trial of moderately to severely active ulcerative colitis in Asia completed to date, with 340 eligible subjects randomized to treatment with etrasimod or placebo. The results demonstrate that treatment with etrasimod 2 mg resulted in a clinically meaningful and statistically significant improvement in the primary and all secondary endpoints. These findings provide strong evidence supporting the use of etrasimod in adult Asian patients with moderately to severely active ulcerative colitis.As Everest’s third commercialized product, VELSIPITY(R) has been officially approved by the Guangdong Provincial Medical Products Administration for adult patients with moderately to severely active UC. It is now available at medical institutions designated under the Connect Policy in the Greater Bay Area. Additionally, Everest has launched a factory construction project at its Jiashan site to support local production of VELSIPITY(R). Copyright 2025 ACN Newswire via SeaPRwire.com.
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Yuexiu REIT Maintains Overall Operational Stability, Achieves Revenue of Over RMB966 Million ACN Newswire

Yuexiu REIT Maintains Overall Operational Stability, Achieves Revenue of Over RMB966 Million

HONG KONG, Aug 14, 2025 - (ACN Newswire via SeaPRwire.com) - Yuexiu Real Estate Investment Trust ("Yuexiu REIT", together with Yuexiu REIT Asset Management Limited, collectively known as the “REIT”; stock code: 405) announced its interim results for the six months ended 30 June 2025.Yuexiu REIT Management Team: Chairman and Non-Executive Director Mr. JIANG Guoxiong (center), Executive Director and Chief Executive Officer Ms. OU Haijing (left), and Chief Financial Officer Mr. KWAN Chi Fai (right)2025 Interim Results Highlights:- Overall operation was stable, with total revenue of RMB966 million (corresponding period of 2024: RMB1,034 million).- As at 30 June 2025, the overall occupancy rate of the properties was 82.2% (corresponding period of 2024: 84.0%).- The average financing cost was 3.33%, representing a decrease of 83 basis points from the beginning of the year. Excluding exchange loss, financing expenses decreased by 13.5% year-on-year.- Interim distribution of approximately RMB0.0333 per unit, equivalent to approximately HK$0.0366. This represents an annualized distribution yield of 8.42%.Guangzhou International Finance Center (GZIFC):- Operating revenue of the GZIFC complex was RMB486 million, accounting for 50.3% of the REIT’s total revenue.- Its office building introduced a Fortune Global 500 company, the occupancy rate was 82.6%, and the renewal rate was 70%.- GZIFC Shopping Mall had a high occupancy rate of 96.4% during the period.- Four Seasons Hotel Guangzhou achieved a 1.1-percentage-point year-on-year increase in average occupancy rate with record room revenue for the period, while Ascott Serviced Apartments GZIFC recorded a 1.8-percentage-point rise in average occupancy and similarly reached historic highs in revenue.Yuexiu Financial Tower:- Yuexiu Financial Tower recorded operating revenue of approximately RMB165 million, representing 17.1% of the REIT’s total revenue. The occupancy rate was 82.1%.- The tenant structure continued to improve, with new introduction of quality tenants such as a Fortune Global 500 company and a futures company with a market value exceeding RMB10 billion.Proactive Management of Financing Risk and Effective Stabilization of Financing Cost- With regard to the short-term loan of RMB530 million and the 5-year syndicated loan of HK$2.1 billion, both due in the first half of 2025, and other loans which are due within the year, the Manager in the first half of 2025 renewed the short-term loan of RMB530 million, obtained offshore loan of RMB1.7 billion and issued dim sum bonds of RMB1 billion for the refinancing and early repayment of the maturing loans so as to ensure effective monitor on the liquidity risk.- The Manager introduced a total of RMB3.23 billion in loans in the first half of 2025 to refinance offshore HKD floating rate loans, taking advantage of the relatively low-cost of RMB financing to proactively adjust the financing structure, thereby minimizing the impact of the interest rate market. At the end of the first half of 2025, the financing interest rate exposure of Yuexiu REIT was approximately 14%, narrowing by 12 percentage points from 26% at the beginning of the year; the average financing cost was 3.33%, representing a decrease of 83 basis points from 4.16% at the beginning of the year; the average interest payment rate for the first half of the year was 3.92%, representing a year-on-year decrease of 64 basis points. Excluding the exchange loss, the finance expenses amounted to approximately RMB402 million, representing a year-on-year decrease of 13.5%.- As at the end of June 2025, Yuexiu REIT had RMB financing of approximately RMB14,795 million, accounting for 72% of total financing (corresponding period of 2024: RMB financing of approximately RMB8,404 million, accounting for 41% of total financing).Mr. JIANG Guoxiong, Chairman and Non-Executive Director of Yuexiu REIT, said, "In the first half of 2025, against the backdrop of global trade volatility and slowing economic growth, China's GDP achieved steady growth of 5.3%, yet corporate expansion remained cautious and slow; retail consumption was weak, and average daily rate of hotel and apartment was under pressure. In order to effectively deal with the headwinds in the industry, we took strategic actions to secure market share by renewing leases in advance, investing in asset appreciation projects to enhance product competitiveness, and effectively stabilizing the fundamentals of operations, which effectively supported the revenue of Yuexiu REIT for the Interim Period. Meanwhile, lower financing cost is beneficial to the distributions.”Guangzhou International Finance Center (GZIFC)GZIFC achieved positive growth in both customer flow and conversion rates through product enhancement and operational optimisation, with a newly contracted area of 13,133 sq.m.. The newly launched 4,235 sq.m. of furnished units recorded an absorption cycle of only about 19 days, with an absorption rate close to 90%. Quality tenants introduced include a Fortune Global 500 company, a leading global shipping company, and a renowned Internet-based culture, sports and entertainment company, taking up more than 2,200 sq.m. in aggregate. In addition, the project recorded a renewed leasing area of 9,099 sq.m. and a renewal rate of 70%, retaining quality tenants including two Fortune Global 500 companies and a foreign consulate. GZIFC was selected as one of the Top 30 companies in the “Performance Index - 2025 Commercial Property Operation Performance” by Guandian.GZIFC Shopping Mall actively created digitalized consumption scenarios, advanced the pilot implementation of the local lifestyle platform “YueXiu Club”, which now covers 12 merchants, while attracting customers through multiple channels such as Dianping and UnionPay QuickPass platforms. Newly contracted area and renewed leasing area totaled 5,734 sq.m., with a renewal rate of 97% and the occupancy rate of 96.4%. During the period, it was announced that China Duty Free Group (CDFG) will set up a store in GZIFC Shopping Mall, which will be the first and currently the only downtown duty-free store in Guangzhou and is expected to open in the third quarter.Room revenue of Four Seasons Hotel Guangzhou and revunue of Ascott Serviced Apartments GZIFC reached a record high for the period, respectively. During the period, the average occupancy rate of Four Seasons Hotel Guangzhou reached 80.1%, representing a year-on-year increase of 1.1 percentage points. The average room rate was RMB2,201, similar to the same period last year. The revenue per available room (RevPAR) was RMB1,762, representing a year-on-year increase of 0.7%. The RevPAR competitive index was 111.7, maintaining a leading market position among luxury hotel competitors. The average occupancy rate of Ascott Serviced Apartments GZIFC reached 92.3%, representing a year-on-year increase of 1.8 percentage point and 9.7 percentage points higher than that of serviced apartment competitors. The average room rate was RMB1,128, similar to the same period last year. The RevPAR was RMB1,041, representing a year-on-year growth of 1.5%. The RevPAR competitive index reached 120.0.Yuexiu Financial TowerDuring the period, Yuexiu Financial Tower recorded a newly contracted area of 7,448 sq.m., including a total of 1,500 sq.m. further took up by seven existing tenants looking for expanded area. 7,089 sq.m. of furnished units were launched, with with an absorption cycle of approximately 38 days and an absorption rate of more than 65%. Quality tenants newly introduced include a Fortune Global 500 company and a futures company with a market value of over RMB10 billion. As certain tenants relocated to their own properties, the project recorded a renewed leasing area of 10,303 sq.m. and a renewal rate of 42%, retaining quality tenants with large leasing areas, including Deloitte, one of the Big Four international accounting firms, and a leading integrated asset management company in China.White Horse BuildingDuring the period, White Horse Building introduced supply chain resources from the Pearl River Delta and recorded a newly contracted area of 3,273 sq.m., with full occupancy on the 1st floor. In the first half of 2025, it welcomed a total of 165 procurement delegations, along with nearly 5,000 purchaser visits, including 23 foreign delegations from France, Vietnam and other countries, and facilitated procurement deals worth RMB140 million. By taking advantage of exhibitions such as the Greater Bay Area International Women’s Wear Expo and the Canton Fair, White Horse Building facilitated tenant transactions. It also successfully launched the cross-border e-commerce platform “White Horse Global E-Channel” and set up a series of courses titled “White Horse Business School Marketing Empowerment Camp” to activate new momentum for tenants’ digital operations.Fortune PlazaDuring the period, the project recorded a newly contracted area of 2,354 sq.m., and introduced quality tenants including several healthcare and elderly care subsidiaries of a Fortune Global 500 integrated financial group. The project recorded a renewed leasing area of 2,924 sq.m. and a renewal rate of 76%, retaining quality tenants including a Fortune Global 500 company, and flexibly adjusted units to match their demand for cost efficiency.City Development PlazaDuring the period, the project recorded a newly contracted area of 7,585 sq.m. and introduced a beauty technology company to enhance the ambience of healthcare business in the building. Retention plans were formulated in light of tenants’ pursuit of cost efficiency, aimed at optimizing product standards to meet tenant needs. The project recorded a renewed leasing area of 2,090 sq.m. and a renewal rate of 68%, retaining tenants including the Guangzhou office of a globally-renowned Contract Research Organisation (CRO).Victory PlazaDuring the period, its anchor tenant, Uniqlo, continued to play a flagship role by launching its C-series products, and hosted the first “A Better Life” campaign of Uniqlo in China, along with gigantic Pokémon installations and A Better Life Music Event, from 28 March to 6 April. Customer flow reached a quarterly peak during the events, driving a 7% year-on-year sales growth in April, and contributing to a 0.3% year-on-year sales growth during the Interim Period. By collaborating with tenants engaged in catering services to capitalize on increased sales with the surge in customer flow, the project drove a year-on-year increase of 0.6% in overall sales during the Interim Period.Shanghai Yue Xiu TowerDuring the period, the project recorded a renewed leasing area of 3,798 sq.m., with a renewal rate of 39%, while securing a newly contracted area of 3,933 sq.m., efficiently making up for the units surrendering ahead of lease expiry. By replacing the energy-saving light tubes in the carpark spaces to enhance brightness, the project enhanced both energy efficiency and service standards, thereby improving tenant satisfaction. As at the end of the Interim Period, the occupancy rate of Shanghai Yue Xiu Tower was 87.2%, representing a year-on-year increase of 2.6 percentage points.Wuhan PropertiesDuring the period, Wuhan Yuexiu Fortune Centre recorded a newly contracted area of 12,395 sq.m., and introduced quality tenants including a member of a leading global automobile group and a diversified professional services company. In addition, it recorded a renewed leasing area of 10,884 sq.m. and a renewal rate of 81%, retaining quality tenants with large leasing areas, including a Fortune Global 500 state-owned enterprise. The business solicitation team optimized the customers’ property visiting experience through partial micro-renovation of units, soft furnishing upgrades and creation of AI model rooms to increase the conversion rate of customers.Starry Victoria Shopping Centre recorded a newly contracted area and renewed leasing area totalling 3,894 sq.m. with a renewal rate of 82% during the period. The project successfully introduced several popular food and beverage brands, including the internet-famous brand “Domino’s” on the 1st floor of Hall A, to attract more family customer groups. The project tapped into nighttime consumption by leveraging the unique appeal of “Joy Garden” on the 4th floor, continuously developing initiatives like “Riverside Starry Night” and “Midnight Diner” to stimulate new sales growth drivers.Hangzhou VictoryHangzhou Victory recorded a newly contracted area of 1,974 sq.m. and introduced a tenant to take up an entire floor during the period. In addition, it recorded a renewed leasing area of 6,083 sq.m. and a renewal rate of 64%, retaining quality tenants including a Fortune Global 500 construction engineering company and the Zhejiang branch of a state-owned enterprise in Shanxi Province.ProspectsThe market generally hopes for further interest rate cuts by the US Federal Reserve in the second half of 2025, though the path and extent remain uncertain. On the other hand, 2025 marks the concluding year of China’s “14th Five-Year Plan”, with policies prioritizing stability, including moderately accommodative monetary policies and “trade-in” consumption subsidy policies aimed at expanding domestic demand to stimulate market vitality. Consequently, the Manager expects the RMB interest rate to remain at a relatively low level. With the accelerated development of new quality productive forces and the advancement of supply-side reforms in China, the Manager expects that new industrial momentum will continue to emerge and business environment will improve. The highly anticipated 15th National Games is scheduled to open in Guangzhou in the second half of 2025, which is expected to boost consumption in shopping malls and demand for hotels and apartments.In the second half of 2025, the Manager will keep abreast of economic development trends and dynamically implement proactive, prudent and flexible leasing strategies, keenly seize potential opportunities, and continuously enhance the market competitiveness of asset portfolio. The Manager will continue to review and make reasonable adjustments to its financing structure depending on expectations of market developments, and introduce low-cost RMB financing through various RMB financing channels to seek more favorable financing costs to offset interest rate risks. Additionally, the Manager will carry out relevant asset appreciation projects as planned, with reasonable planning and phased renovation of the guest rooms at Four Seasons Hotel Guangzhou. By focusing on product enhancement, equipment renewal and safety guarantee, the Manager aims to achieve value preservation and appreciation of the properties and ensure the sound operation of the projects.About Yuexiu Real Estate Investment TrustYuexiu Real Estate Investment Trust ("Yuexiu REIT") was listed on the Hong Kong Stock Exchange of Hong Kong Limited on 21 December 2005 and is the first listed real estate investment trust only investing in properties in the People's Republic of China (the "PRC") in the world. The current property portfolio comprises ten high quality properties, namely Guangzhou International Finance Center, White Horse Building, Fortune Plaza, City Development Plaza, Victory Plaza, Yuexiu Financial Tower in Guangzhou, Yuexiu Tower in Shanghai, Wuhan Properties in Wuhan (including Wuhan Yuexiu Fortune Centre and Starry Victoria Shopping Centre), Victory Business Centre in Hangzhou and Yuexiu Building in Hong Kong, with a total area of ownership of approximately 1.184 million sq.m. All properties are located in the central business district of Guangzhou, Shanghai, Wuhan, Hangzhou and Hong Kong respectively. The categories of the properties include Grade-A offices, commercial complexes, retail business, hotel, serviced apartments and professional clothing market etc.For media enquiries:Strategic Financial Relations LimitedVicky LeeTel: +852 2864 4834Email:sprg_yx@sprg.com.hk Phoebe LeungTel: +852 2114 4172 Maggie ZhangTel: +852 2864 4903 Websitehttp://www.sprg.com.hk Copyright 2025 ACN Newswire via SeaPRwire.com.
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艾曲莫德入选《2025 ACG临床指南:成人溃疡性结肠炎》,获强烈推荐用于中重度溃疡性结肠炎的诱导缓解及维持缓解治疗 ACN Newswire

艾曲莫德入选《2025 ACG临床指南:成人溃疡性结肠炎》,获强烈推荐用于中重度溃疡性结肠炎的诱导缓解及维持缓解治疗

香港,2025年8月15日 - (亚太商讯 via SeaPRwire.com) - 云顶新耀今日宣布,旗下创新药艾曲莫德(VELSIPITY(R),etrasimod)被纳入《2025 ACG 临床指南:成人溃疡性结肠炎》(下称"新版指南"),并获得强烈推荐用于中重度活动性溃疡性溃疡性结肠炎(UC)患者的诱导缓解及维持缓解治疗(中等质量证据)。新版指南同时建议,对于已通过鞘氨醇-1-磷酸(S1P)受体调节剂实现诱导缓解的患者,继续使用艾曲莫德以维持缓解(强烈推荐,中等质量证据)。这一重要进展不仅体现了国际权威医学指南对艾曲莫德临床价值的高度认可,也进一步彰显了其在满足UC患者未被满足的治疗需求方面的潜力,为全球UC患者提供新的治疗选择。此次新版指南由美国胃肠病学会(American College of Gastroenterology,ACG)制定,基于近五年最新循证医学证据,系统总结了UC治疗及并发症预防的新方法与新进展,为临床医生提供规范、科学的管理参考,以更好地应对不同程度的UC患者治疗需求。新版指南指出,艾曲莫德作为新一代高选择性S1P受体调节剂,通过将活化的淋巴细胞滞留于淋巴结中,减少其在肠道中的浸润,从而降低局部炎症反应,并伴随外周循环淋巴细胞计数下降。艾曲莫德ELEVATE UC III 期注册研究(ELEVATE UC 52和ELEVATE UC 12)这两项随机、双盲、安慰剂对照研究均达到了所有主要和关键次要终点,分别在第12周和第52周显著改善临床缓解率,并实现持久的内镜下深度黏膜愈合。值得注意的是,研究中100%的临床缓解均为无激素缓解,安全性良好,与既往研究结果一致。指南也特意强调了与其他现有治疗不同的是,艾曲莫德 ELEVATE UC III 期注册研究中纳入了溃疡性直肠炎,且证实了在此类人群中显著提升了临床缓解率(治疗12周时,43.2% vs 13.6%, p<0.001)。此前,艾曲莫德还被纳入2024年美国胃肠病学协会(AGA)临床实践指南, 推荐作为溃疡性结肠炎的一线治疗。艾曲莫德亚太临床试验牵头研究者、世界胃肠病学会司库、亚太消化病学会副主席、中华医学会第十届消化病学分会副主任委员、中国人民解放军第四军医大学附属西京医院吴开春教授表示:"新版指南进一步明确,'实现内镜黏膜愈合以达成持续无激素缓解和避免住院手术'是中重度溃疡性结肠炎治疗的核心目标,这不仅关系到疾病的长期安全管理,也与改善患者生活质量息息相关。此次指南中,艾曲莫德被强烈推荐用于中重度活动性溃疡性结肠炎的诱导和维持治疗,标志着其临床价值获得了国际权威学术机构的高度认可,也为临床实践提供了全新的治疗选择。"云顶新耀首席执行官罗永庆表示:"艾曲莫德此次获新版指南强烈推荐用于中重度活动性溃疡性结肠炎的诱导和维持治疗,充分体现了其卓越的临床疗效和良好安全性,进一步确立了其作为一线治疗新选择的重要地位。新版指南明确将实现内镜黏膜愈合作为治疗中重度活动性溃疡性结肠炎的核心目标,印证了黏膜愈合为国内外指南一致认定的重要终点,可显著降低疾病复发、住院、结直肠切除及结直肠癌风险。值得一提的是,指南特别强调了艾曲莫德在溃疡性直肠炎患者中同样可显著提升临床缓解率。在亚洲,溃疡性结肠炎患者人数持续上升,以中国为例,2024年中国的溃疡性结肠炎患者数量约为80万人,预计到2030年将达100万人,现有临床治疗选择有限,迫切需要兼顾疗效、安全性与便利性的创新方案。我们将加速艾曲莫德的商业化进程,助力更多患者长期维持安全有效的疾病缓解,并提升生活质量。"作为云顶新耀在自身免疫疾病领域布局的核心创新产品,艾曲莫德(维适平(R))的新药上市申请已于2024年12月获中国国家药品监督管理局正式受理,预计今年年底或明年年初获批。艾曲莫德已在新加坡、中国澳门和中国香港获批,其新药上市许可申请也已在韩国和中国台湾地区获正式受理。艾曲莫德已被纳入粤港澳大湾区内地9市临床急需进口港澳药品医疗器械目录(2024年),在大湾区先行使用,成为云顶新耀第三款商业化新药。云顶新耀已于2025年3月启动艾曲莫德在嘉善工厂的本地化生产建设项目,支持其在大中华区及其他亚洲市场的供应及商业化落地。 Copyright 2025 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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卫龙美味公布2025年中期业绩 ACN Newswire

卫龙美味公布2025年中期业绩

香港,2025年8月14日 - (亚太商讯 via SeaPRwire.com) - 中国辣味休闲食品行业龙头企业,卫龙美味全球控股有限公司("卫龙美味"或"集团")及附属公司("集团")( 香港联交所股票代码:09985)公布截至2025年6月30日止六个月("期内")之中期业绩。人民币截至6月30日止六个月2025年2024年变动收入34.83亿29.39亿+18.5%毛利16.42亿14.62亿+12.3%毛利率47.2%49.8%-2.6个百分点期内净利润7.36亿6.21亿+18.5%净利润率21.1%21.1%保持稳定中期股息0.18元/普通股0.16元/普通股+12.5%2025年上半年,在全球消费增长普遍承压下,中国消费市场依然是全球最大消费市场之一。 得益于中国休闲食品市场近年来呈现出稳健的增长态势,报告期内,卫龙美味紧跟行业发展趋势,坚持多品类产品策略,聚焦创新,深度开展消费者洞察,精准捕捉市场需求,持续强化研发实力,并持续以年轻人喜爱的方式深化品牌渗透,通过各种线上线下的品牌活动搭建多维消费场景链接深化品牌渗透,持续推进全渠道覆盖能力和销售网络,进而为客户及消费者提供更好的服务和体验。报告期内,卫龙美味经营策略成效彰显,业绩持续稳健攀升,收入与净利润均录得双位数增长。2025年上半年实现总收入34.83亿元(人民币,下同),同比增长18.5%,主要由于集团期内持续加强全渠道和品牌建设,并优化渠道结构。尽管报告期内部分原材料成本上涨导致集团毛利率由去年同期的49.8%下降2.6个百分点至47.2%,但在收入增长及集团积极提升供应链效率的共同因素驱动下,毛利仍同比增长12.3%至16.42亿元。同时受惠于集团经营利润的提升,集团期内净利润同比增长18.5%至7.36亿元;净利润率得以维持去年同期水平,为21.1%。基于期内整体绩效表现,集团董事会决议派发2025年中期股息每股人民币0.18元,派息比率约为60%,预计派付股息日期为2025年10月20日或前后。产品方面,集团坚持多品类产品策略,从新产品、新口味、新工艺、新包装等维度发力,如拓展风味创新边界,深度回应消费者对创新口味的需求。2025上半年,集团先后先后推出了麻酱口味"魔芋爽"以及麻辣牛肉口味"亲嘴烧"等多个新品,进一步拓展并丰富产品组合,提升产品品质,满足市场多元化及个性化的消费需求,驱动产品力与市场需求匹配。品牌建设方面,集团持续以年轻人喜爱的方式深化品牌渗透,透过各种线上线下的品牌活动搭建多维消费场景链接,譬如联合林里柠檬茶发起"爆辣挑战",凭借爆款销量与话题效应触达更多消费者;携手国潮品牌哭喊中心推出"大儿童专属"系列,借节日营销勾起青春味觉记忆。此外,集团于报告期内官宣王安宇担任魔芋爽代言人,借力明星影响力拓宽传播路径。集团的一系列举措有效触达年轻客群,夯实了品牌年轻化与趣味化的发展根基。渠道方面,集团持续推进线下全渠道、线上全平台覆盖策略。随着各种新兴渠道业态的兴起,集团紧跟渠道变化,持续拓展终端网点,强化销售团队终端执行力,并联合经销商持续提升终端的服务能力和产品铺市率,从而有力推动线下终端业绩稳步增长。在线上领域,集团同样积极布局,构建全平台生态体系,确保与线下渠道形成有效联动,助力全渠道发展战略落地。此外,集团始终致力于生产设施的自动化升级与技术创新突破,同步加快各业务系统的数字化转型进程。在此基础上,集团不断强化组织发展与核心人才梯队建设,以此全面提升公司整体运营效能,为业务的持续稳健发展注入强劲动力。卫龙美味董事长刘卫平先生表示:"集团将始终坚守"多品类"产品策略,坚持产品创新,持续加码品牌建设力度,不断强化卫龙"年轻、有趣、有创意"的品牌形象与独特调性。与此同时,集团积极拥抱变化,持续加强全渠道的覆盖能力,为消费者提供更便捷的消费体验。展望未来,集团将以更积极、更主动的心态拥抱市场的变化,以更好的产品、更优质的服务和体验不断提升我们的竞争力,持续为消费者、客户、员工、投资人及社会创造更大的价值。"关于卫龙美味全球控股有限公司卫龙美味全球控股有限公司("卫龙美味")是中国领先的集研发、生产及销售为一体的辣味休闲食品企业,拥有强劲的增长势头和颇具影响力的品牌。 卫龙美味以传统美食为基础开创了中国调味面制品(俗称辣条)行业,于2001年开创出第一根辣条,并引领了辣条行业标准建设。 凭借出众的品类拓展能力,本集团已成功扩展至蔬菜制品、豆制品及其它产品等品类,推出了包括魔芋爽、风吃海带、小魔女等大单品。 卫龙美味是倍受中国年轻消费者喜爱的休闲食品品牌,拥有有效触达年轻消费者的全渠道销售及经销网络。 如欲获得更多信息,请浏览: https://www.weilongshipin.com/。 Copyright 2025 亚太商讯 via SeaPRwire.com.
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越秀房产基金整体经营稳定 实现收入逾人民币9.66亿元 ACN Newswire

越秀房产基金整体经营稳定 实现收入逾人民币9.66亿元

香港,2025年8月14日 - (亚太商讯 via SeaPRwire.com) - 越秀房地产投资信托基金(「越秀房产基金」,连同越秀房托资产管理有限公司,统称「基金」;股份代号:405)公布其截至2025年6月30日止六个月之中期业绩。越秀房产基金管理团队:主席及非执行董事江国雄先生(中)、执行董事及行政总裁区海晶女士(左)、财务总监关志辉先生(右)2025年中期业绩摘要:- 整体经营稳定,收入总额为人民币9.66亿元(2024年同期:人民币10.34亿元)。- 于2025年6月30日,物业整体出租率为82.2%(2024年同期:84.0%)。- 平均融资成本为3.33%,较年初下降83个基点,剔除汇兑亏损的融资成本同比减少13.5%。- 中期分派每个基金单位约人民币0.0333元,约等于0.0366港元。按年计算的分派收益率为8.42%。广州国金中心:- 广州国金中心综合体录得经营收入为人民币4.86亿元,占基金收入总额50.3%。- 广州国金中心写字楼引进一家财富世界500强背景企业;出租率为82.6%;续约率为70%。- 国金天地期内出租率高达96.4%。- 广州四季酒店平均入住率同比上升1.1个百分点,客房收入创历史同期新高;国金中心雅诗阁服务式公寓平均入住率同比增长1.8个百分点,营业收入亦创历史同期新高。广州越秀金融大厦:- 越秀金融大厦录得经营收入约人民币1.65亿元,占基金收入17.1%,出租率达82.1%。- 租户结构不断优化,新引进优质租户包括一家财富世界500强背景企业,以及一家市值超百亿的期货企业。积极管理融资风险,有效平抑融资成本- 针对2025年上半年到期的人民币5.3亿元短期贷款、21亿港元5年期银团贷款及今年内到期的其他贷款,管理人于2025年上半年完成人民币5.3亿元短期贷款续借,并通过取得人民币17亿元境外贷款和发行人民币10亿元点心债,用于到期贷款的再融资及提前置换,确保流动性风险得到有效管控。- 管理人期内合计引入人民币32.3亿元贷款,并置换境外浮息港元贷款,利用人民币融资相对低位,主动调节融资结构,降低利率市场冲击。2025年上半年末融资利率敞口约为14%,较年初26%收窄12个百分点;平均融资成本为3.33%,较年初4.16%下降83个基点;上半年平均付息率3.92%,同比下降64个基点。剔除汇兑亏损的融资成本约为人民币4.02亿元,同比减少13.5%。- 2025年6月末人民币融资约147.95 亿元,占总体融资72%(2024年同期:人民币融资约84.04 亿元,占总体融资41%)。越秀房产基金主席及非执行董事江国雄先生表示:「2025年上半年,在全球贸易环境波动及经济增长放缓的背景下,中国国内生产总值GDP同比增长5.3%,但企业扩张保守缓慢;零售消费疲弱、酒店公寓房价承压。为应对行业不利因素,我们策略性抢占市场份额,提前推进续租工作,投入资本性改造,提升产品竞争力,有效稳住经营基本面,为中期经营收入提供坚实支撑。同时,融资成本回落也为分派创造有利条件。」国金中心国金中心透过提升产品和优化营运,客户访问量和转化率均录得正向提升,新签13,133平方米。推出4,235平方米带装修单元去化周期仅约十九天,去化率接近九成。引进优质租户包括一家财富世界500强背景企业、一家全球龙头航运企业和一家知名互联网背景文体娱乐企业,合计超过2,200平方米。续租9,099平方米,续租率70%,留存优质租户包括两家财富世界500强背景企业和一家外国领事馆。国金中心入选观点「表现力指数·2025商办资产运营表现」TOP30榜单。国金天地积极打造电子化消费场景,推进悦秀会本地生活平台试点落地,已覆盖12家商户,同时利用大众点评、云闪付等平台多渠道引流,新签和续租合计5,734平方米,续租率97%。出租率为96.4%。期内,中免免税店宣布落户国金天地,预计第三季度开业,成为广州首家且目前唯一的市内免税店。广州四季酒店客房收入和国金中心雅诗阁服务式公寓营业收入分别创历史同期新高。广州四季酒店期内平均入住率为80.1%,同比上升1.1个百分点;平均房价为人民币2,201元,与去年同期相若;每间可供出租客房收入(RevPAR)为人民币1,762元,同比增长0.7%;RevPAR竞争指数为111.7,在奢华酒店竞争群组中始终保持较领先的市场地位。国金中心雅诗阁服务式公寓期内平均入住率为92.3%,同比上升1.8个百分点,平均入住率高于竞争群公寓9.7个百分点;平均房价为人民币1,128元,与去年同期相若;RevPAR为人民币1,041元,同比增长1.5%;RevPAR竞争指数达120.0。越秀金融大厦越秀金融大厦期内新签7,448平方米,包括七家租户扩租合计1,500平方米。推出7,089平方米带装修单元,去化周期约38天,去化率超过六成半。新引进优质租户包括一家财富世界500强背景企业,以及一家市值超百亿的期货企业。受部分租户回迁自有物业办公的影响,续租10,303平方米,续租率42%。留存大面积优质租户包括国际四大之一「德勤」和一家国内龙头综合性资产管理公司。白马大厦白马大厦引入珠三角供应链资源,期内带动新签3,273平方米,实现一楼满租。上半年累计接待165个采批团,累计接待采购商近5,000人次,其中包括来自法国、越南等23个外商团,促成采购金额达人民币1.4亿元。白马大厦依托大湾区国际女装展、广交会等展会促进租户成交,亦成功推出「白马悦境通」跨境电商平台和「白马商学院营销赋能营」系列课程,激活租户数字化运营新动能。财富广场财富广场期内新签2,354平方米,引进优质租户包括一家财富世界500强综合金融集团旗下医疗养老板块的数家企业。续租2,924平方米,续租率76%,留存优质租户包括一家财富世界500强背景企业,亦灵活匹配降本需求调整单元挽留租户。城建大厦城建大厦期内新签7,585平方米,引进一家美容科技企业提升楼内大健康业态氛围。结合租户降本意愿制定挽留方案,优化产品标准匹配租户需求。续租2,090平方米,续租率68%,包括一家全球知名合同研究组织(CRO)的广州办公室。维多利广场维多利广场期内主力租户「优衣库」继续发挥旗舰作用,首发C系列产品,并于3月28日至4月6日落地全国首场「优衣库美好生活市集」、巨型宝可梦及美好生活音乐活动,活动期间达季度客流峰值,带动四月销售额同比增长7%,推动中期期间销售额同比增长0.3%。项目联动餐饮租户,抓住客流高峰提升销售,带动中期期间项目整体销售额同比增长0.6%。上海越秀大厦上海越秀大厦期内续租3,798平方米,续租率39%;新签3,933平方米,迅速填补退租单元。通过更换停车场节能灯管提升场内亮度,项目实现节能效益和服务水平双提升,提高租户满意度。于中期期末,上海越秀大厦出租率为87.2%,同比增加2.6个百分点。武汉物业武汉越秀财富中心期内新签12,395平方米,引进优质租户包括一家全球领先汽车集团成员企业和一家多元化专业服务企业。续租10,884平方米,续租率81%,留存大面积优质租户包括一家财富世界500强背景央企。招商团队透过单元局部微改造、软装提升、打造智能样板间等多种方式优化客户看楼体验,提升客户转化率。星汇维港购物中心期内新签和续租合计3,894平方米,续租率82%。成功引进多家热门餐饮品牌,包括A馆一楼引进网红品牌「达美乐」,带动更多家庭客群。项目开拓夜间消费,利用四楼「悦花园」亮点优势,持续打造「江畔星夜」、「深夜食堂」激发销售新增长点。杭州维多利杭州维多利期内新签1,974平方米,引进一家全层租户。续租6,083平方米,续租率64%,留存优质租户包括一家财富世界500强背景建筑工程企业和一家山西省属国企的浙江分公司。未来展望市场普遍憧憬美联储下半年进一步降息,但路径和幅度仍具不确定性。另一方面,今年是中国「十四五」规划收官之年,各项政策稳字当头,包括适度宽松货币政策和「以旧换新」消费补贴政策,旨在通过扩大内需激发市场活力,因此管理人预期人民币利率将维持较低水平。伴随国内新质生产力加快培育发展和供给侧改革深化推进,管理人预期产业动能继续推陈出新,营商气氛将向好改善。备受瞩目的第十五届全国运动会将于下半年在广州开幕,有望带动商场消费和酒店公寓需求。下半年,管理人将因应经济发展走势动态实施积极、稳健、灵活的租赁策略,敏锐把握潜在机会,持续提升资产组合市场竞争力。管理人将视市场发展预期对融资结构持续检视并进行合理调整,通过各类人民币融资途径,引入低成本人民币融资,以寻求更优融资成本,平滑利率风险。管理人将按计划开展相关资本性改造工程,合理规划和分段改造广州四季酒店客房,围绕产品提升、设备更新和安全保障维度,实现物业保值增值,为项目稳健经营保驾护航。关于越秀房地产投资信托基金越秀房地产投资信托基金(「越秀房产基金」)于2005年12月21日在香港联交所上市,为全球首只投资于中国内地物业的上市房地产投资信托基金。越秀房产基金目前持有的物业组合包括位于广州的广州国际金融中心、白马大厦、财富广场、城建大厦、维多利广场、越秀金融大厦、位于上海的越秀大厦、位于武汉的武汉物业(包括武汉越秀财富中心和星汇维港购物中心)、位于杭州的维多利商务中心以及位于香港的越秀大厦共10项高素质物业,物业产权面积共约118.4万平方米,分别位于中国广州市、上海市、武汉市、杭州市及香港市的核心商业区域。物业类型包括甲级写字楼、商业综合体、零售商业、酒店、服务式公寓、服装专业市场等。传媒查询:纵横财经公关顾问有限公司李惠儿电话: +852 2864 4834电邮:sprg_yx@sprg.com.hk梁家仪电话: +852 2114 4172张铭伊电话: +852 2864 4903网址:http://www.sprg.com.hk Copyright 2025 亚太商讯 via SeaPRwire.com.
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云顶新耀维长宁(艾曲莫德)在中国台湾新药上市申请获受理 亚洲市场准入再迎里程碑 ACN Newswire

云顶新耀维长宁(艾曲莫德)在中国台湾新药上市申请获受理 亚洲市场准入再迎里程碑

香港,2025年8月14日 - (亚太商讯 via SeaPRwire.com) - 云顶新耀今日宣布,中国台湾地区药政主管部门(TFDA)已正式受理维长宁(艾曲莫德,中国台湾地区商品名:"維長寧")用于治疗中重度活动性溃疡性结肠炎(UC)患者的新药上市许可申请(NDA)。这一进展标志着艾曲莫德继在中国澳门、新加坡和中国香港获批以及韩国NDA获正式受理之后,在亚洲市场的准入取得又一重大里程碑。中国国家药品监督管理局也于2024年12月正式受理艾曲莫德(维适平(R))的新药上市申请,预计将在今年年底或明年年初获批。艾曲莫德是一款针对溃疡性结肠炎,每日一次的口服一线治疗药物,能够强效实现肠道黏膜愈合,且使用便捷,并具有良好的安全性特征。黏膜愈合是国内外溃疡性结肠炎临床指南一致认定的溃疡性结肠炎治疗目标。溃疡性结肠炎患者尽早实现黏膜愈合,可大幅降低疾病复发率、住院率、结直肠切除手术率和结直肠癌发生风险。艾曲莫德已被纳入2024年美国胃肠病学协会(AGA)临床实践指南, 推荐作为溃疡性结肠炎的一线治疗。2025年,艾曲莫德获得2025年美国胃肠病学会(ACG)成人UC临床指南的一线治疗推荐,进一步印证了其全球专业共识下的临床价值。云顶新耀首席执行官罗永庆先生表示:"此次在中国台湾地区NDA申请的正式受理,是维长宁亚洲商业化进程中的又一重要进展。随着亚洲地区溃疡性结肠炎患者人数持续增长,临床上存在巨大未满足需求。仅在中国,2024年溃疡性结肠炎患者数量约为80万人,预计到2030年将达100万人。患者面临长期治疗与生活质量的双重挑战。此次受理充分体现了对维长宁临床价值的高度认可。我们将继续加快这一创新疗法在中国大陆及亚洲其他市场的上市进程,提升可及性,帮助患者实现长期疾病控制并改善生活质量。"本次申请基于ELEVATE UC III期注册研究(ELEVATE UC 52和ELEVATE UC 12)和ENLIGHT研究(ES101002)的结果。ELEVATE UC III期注册研究显示,在既往常规治疗、生物制剂或JAK抑制剂治疗失败或不耐受的中重度活动性溃疡性结肠炎患者中,每日一次2mg艾曲莫德在第12周和第52周均显示卓越且持久的临床缓解和内镜下深度黏膜愈合,且安全性良好,与既往研究一致。同时,ENLIGHT研究作为迄今最大规模的亚洲中重度UC III期注册临床研究,在中国大陆、中国台湾及韩国开展,共纳入340名患者。研究结果显示,艾曲莫德在诱导期和维持期均取得了显著且具有统计学意义的疗效优势,为其在亚洲人群中的应用提供了有力证据支持。作为云顶新耀在自身免疫性疾病领域的重磅产品,艾曲莫德已于2024年被纳入粤港澳大湾区内地9市临床急需进口港澳药品医疗器械目录,在大湾区先行使用,惠及UC患者,并成为公司第三款商业化新药。今年3月,云顶新耀已启动艾曲莫德在嘉善工厂的本地化生产建设项目,以支持其在大中华区及亚洲其他市场的供应与商业化落地。 Copyright 2025 亚太商讯 via SeaPRwire.com.
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业聚医疗2025年中期业绩收入及纯利双双增长 分别达8,360万美元及1,980万美元 ACN Newswire

业聚医疗2025年中期业绩收入及纯利双双增长 分别达8,360万美元及1,980万美元

业绩亮点:- 收入达83.6百万美元,同比增长5.9%。- 销量达919,000件,其中779,000件为自有产品,同比增长8.6%。- 公司拥有人应占利润同比上升5.1%至19.8百万美元。- 核心经营利润达15.1百万美元,同比增长11.4%。- 为庆祝集团成立25周年,董事会宣派特别股息每股15港仙。- 财务状况稳健,截至2025年6月30日,现金及银行结余达237.1百万美元,支持潜在收购及新生产设施建设。- 优质产品获全球广泛认可,带动亚太地区市场收入按年增长14.0%,欧洲、中东及非洲市场增长17.0%,及美国市场增长20.0%。- 于上半年收购一家台湾经销商,并计划下半年于比利时及荷兰设立直销团队,进一步加强在亚太地区及欧洲、中东及非洲市场的影响力。- 集团善用全球商业化专长及庞大销售网络,与医疗器械同业建立战略合作,藉此丰富产品组合,并透过交叉销售创造额外收入。香港,2025年8月15日 - (亚太商讯 via SeaPRwire.com) - 专营经皮冠状动脉介入治疗(PCI)及经皮腔内血管成形术(PTA)手术介入器械的全球医疗器械制造公司业聚医疗集团控股有限公司("业聚医疗"或"集团";股份代号:6929)今天宣布截至2025年6月30日止六个月("报告期")的中期业绩。尽管宏观经济环境未见明朗,集团的收入及纯利仍双双录得增长。美国市场增长强劲,加上亚太地区及欧洲、中东与非洲地区新兴市场的持续贡献,推动集团收入达到83.6百万美元,较去年同期上升5.9%。核心经营利润(自本公司拥有人应占利润撇除以股份为基础的薪酬开支、与税务亏损相关的递延税项资产的税务抵免净额及融资收入╱成本)为15.1百万美元,同比增长11.4%。公司拥有人应占利润同比上升5.1%至19.8百万美元。每股基本盈利为2.40美仙(2024年上半年:2.28美仙)。截至2025年6月30日,集团财务状况保持稳健,现金及银行结余达237.1百万美元。鉴于集团的财务状况稳健,以及为庆祝成立25周年,董事会议决宣派特别现金股息每股普通股15港仙,彰显集团致力为股东创造价值。连同截至2024年12月31日止年度之末期股息每股10港仙(已于2025年6月16日派付),股东于2025年合共获派股息每股25港仙。业聚医疗董事长、执行董事兼首席执行官钱永勋先生表示:"过去25年,我们持续投资于创新及全球商业化能力,除了为业聚医疗建立了声誉,也助我们在不同的经济周期中破浪前行。尽管2025年上半年面临宏观经济及地缘政治的双重挑战,我们的全球布局仍展现韧性。美国市场增长印证了市场对我们的优质产品需求殷切,而我们亦透过庞大的销售网络,成功把握了亚太地区及欧洲、非洲及中东地区的增长机遇。我们将继续透过直销市场覆盖、卓越的销售支援、对创新的投入,以及全面的PCI和PTA产品组合提升品牌价值,从而强化竞争优势,为医生及患者提供更安全有效治疗方案的同时,也为股东创造长远回报。"全球销售网络及合作伙伴关系推动收入增长业聚医疗已建立覆盖逾70个国家及地区的销售网络,在13个地区设立直销团队并建立全球经销商网络,成为把握各地机遇、回应当地需求的重要一环。期内,受惠于印尼市场增长,以及Scoreflex TRIO 在新加坡及马来西亚获更广泛采用,亚太地区收入同比上升14.0%至27.3百万美元。欧洲、中东及非洲市场方面,德国、法国及西班牙等直销市场及包括英国、斯洛伐克及捷克共和国在内的分销市场的自有球囊类产品销售表现强劲,带动该区收入上升17.0%至22.4百万美元。尽管受关税因素影响,美国市场收入仍同比上升20.0%至8.0百万美元,主要受冠脉的普通及刻痕球囊,包括高价产品Scoreflex NC球囊,以及外周球囊销量显著上升所推动。而日本及中国境内市场的收入分别为16.1百万美元及9.7百万美元。凭借其广受认可的全球商业化能力,集团与立志走向国际巿场的同业合作,藉此丰富产品组合并开拓额外收入来源。继去年与深圳开立生物医疗科技股份有限公司成功展开合作,在香港及澳门分销血管内超声产品后,集团与该伙伴再度签订独家分销协议,在新加坡及马来西亚分销相关产品。至目前为止,合作范围已进一步扩展至集团旗下位于欧洲的4个直销市场,包括法国、德国、西班牙及瑞士,及其他6个分销市场。性能主导的多元化创新产品组合,提升市场差异化水平截至2025年6月30日,业聚医疗在全球主要司法管辖区拥有逾250项授权专利及已公布专利申请,及逾55款获批产品。期内,集团产品注册及临床试验继续取得进展,包括:- Sapphire 3的美国临床试验进展顺利,预期于2025年第四季度完成病人入组,以支持该产品的FDA纳入CTO适应症,从而与市场上其他传统半顺应性球囊形成差异化;- JADE PLUS及Teleport Glide获得CE标志、Teleport Glide及Scoreflex QUAD获得PMDA批准、COREPASS模组化微导管获得FDA批准、导引导管获得国家药监局批准;- 就Scoreflex TRIO、Sapphire ULTRA、Sapphire NC ULTRA、Sapphire NC 24、JADE PLUS、Teleport XT及Teleport Glide向国家药监局提交注册申请,并就Vascuaid抽吸导管及大管腔延长导管向PMDA提交注册申请。集团拥有庞大的产品管线。在冠状动脉领域,Sapphire PTX紫杉醇药物涂层球囊大约于2025年底在日本展开临床研究;外周方面,JADE Score球囊则预期于2026年向PMDA提交注册申请。合资企业业聚培福在中国境内展开的TricValve临床试验亦取得重大进展,参与医院数量上升,加快了病人入组进度。此外,业聚培福亦正透过"港澳注册药品及医疗器械进入大湾区计划",积极推动大湾区各大医院采用TricValve。TricValve于2025年7月完成首次在中国境内进行的商业化植入手术,达到重要的里程碑。多区域生产基地缓解地缘政治风险截至2025年6月30日,业聚医疗于中国深圳、荷兰荷佛拉肯,以及德国莱茵河畔魏尔设有生产基地,总年产能约为210万件球囊及支架。自2023年底收购eucatech AG以来,集团已投入资源恢复其生产能力,期内产量逐步提升,以供应销售及临床注册所需产品。2025年8月,集团完成位于中国杭州、旗下最大研发及生产基地的主体结构建设,装修工程预期于下半年展开。该基地计划于2027年投产,届时将新增年产能240万件。钱先生总结说:"有见于新兴市场的强劲势头、自研产品陆续成功推出巿场,以及已建立的战略合作,我们对2025年下半年前景保持乐观。除了亚太地区及欧洲、中东及非洲将继续担当主要的增长引擎,我们亦计划将部分市场由分销模式转为直销模式,以强化当地营收能力及市场渗透。欧洲市场将透过于比利时及荷兰设立直销团队加强市场影响力;日本市场则藉新产品上市重拾增长动力;而在中国境内市场,我们则把握政策支持,扩大产品覆盖并加速商业化进程。随着关税争端缓和,美国市场的产品交付亦有望加快。凭借业聚医疗多元化的产品组合、稳健的财务状况及规模经济效益,我们具备优势构建具韧性及竞争力的业务体系,为持份者创造可持续的价值。"关于业聚医疗集团控股有限公司业聚医疗是一家全球医疗器械制造公司,专门生产用于经皮冠状动脉介入治疗(PCI)及经皮腔内血管成形术(PTA)的介入器械。本集团总部位于中国香港,产品销往全球超过70个国家和地区。集团亦积极将业务扩展至结构性心脏病领域。凭借拥有逾20年产品开发经验的内部研发团队,本集团已开发出世界领先的专有技术。如需了解更多详情,请访问集团官网:https://orbusneich.com/ Copyright 2025 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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广发证券荣膺国家数据管理能力成熟度(DCMM)最高等级认证 ACN Newswire

广发证券荣膺国家数据管理能力成熟度(DCMM)最高等级认证

广州,2025年8月15日 - (亚太商讯 via SeaPRwire.com) - 近日,中国电子信息行业联合会公布最新一批获颁数据管理能力成熟度(简称"DCMM")等级证书企业名单,广发证券获评最高等级五级(优化级)认证,成为行业首家获评最高等级的证券公司,标志着公司在数据管理和应用方面达到国内领先水平,为行业数据管理能力建设树立标杆。《数据管理能力成熟度评估模型》(GB/T 36073-2018)是我国数据管理领域正式发布的首个国家标准。该认证从数据战略、数据治理、数据架构、数据应用等多个维度,全面评估企业的数据管理能力。其中,五级(优化级)作为最高等级,标志着企业的数据管理已形成行业最佳实践,具备强大的示范引领作用。一直以来,广发证券高度重视数据管理能力的建设与提升,将数据视为企业核心资产。公司构建了"战略引领、全员参与、跨部门协同、全生命周期管理"的数据管理体系。通过制定清晰的数据战略规划,完善数据治理组织架构与制度流程,强化数据安全与合规管理,持续提升数据质量与应用效能,公司实现了数据管理从"规范"到"优化"的跨越式发展,为业务创新、客户服务升级及风险管理提供了强有力的数据支撑。广发证券副总经理、首席信息官辛治运表示:"公司将以此次获得DCMM五级认证为新的起点,持续深化数据管理能力建设,进一步完善数据治理长效机制,推动数据技术与业务场景的深度融合,并以此为契机,不断提升服务实体经济的质效,为证券行业的数据管理创新与发展贡献更多力量。" Copyright 2025 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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RAK ICC以2025年立法升级加强基金会制度 ACN Newswire

RAK ICC以2025年立法升级加强基金会制度

阿联酋拉斯海马市, 2025年8月14日 - (亚太商讯 via SeaPRwire.com) - 阿勒哈伊马国际公司注册中心(RAK ICC)宣布对其2019年《基金会条例》进行重大修订,新规已于2025年7月31日生效。此次修订是该制度自推出以来最为重要的更新之一,进一步巩固了阿联酋作为财富架构与长期资产保护竞争性司法辖区的地位。RAK ICC基金会因其灵活性、保密性及法律稳健性而广受认可,成为阿联酋国内外高净值人士、企业家及家族办公室的首选架构工具。这类结构通常用于继承规划、家族治理,以及将多元化资产整合于单一法律实体之下。2025年的修订引入了更强的法律保障及改进的治理措施,包括:1. 防火墙条款 —— 对与RAK ICC法规相冲突的外国判决提供更强有力的保护。2. 三年诉讼时效 —— 将对基金会设立或资产转移提出异议的时限限制为三年。3. 诉因条款 —— 债权人欺诈索赔仅限于涉案的特定资产,且仅在该行为导致创办人资不抵债时才适用。4. 胁迫与高管保护 —— 宣告在外国法律胁迫下采取的行为无效,从而保障基金会内部治理的自主权。5. 强化仲裁机制 —— 允许通过具备法院级权力的私下仲裁方式解决争议。6. 私人受托基金会条款 —— 明确基金会作为受托人持有财产时的资产隔离及受信义务的完整性。在RAK ICC基金会持有的资产现将享有更强的防火墙保护,确保与阿联酋法律相冲突的外国判决无法对其执行。新规设立了三年的时效期,用于限制对基金会成立或资产转入的质疑,为创办人及受益人提供更大的确定性。改革还收紧了债权人保护规则,在欺诈性转让索赔中须证明创办人资不抵债,并将责任限定在争议资产的价值范围内,以防涉及无关财产。此外,修订后的法规着重维护治理完整性和运营韧性。基金会高管在收到与RAK ICC法律不一致的外国命令时,必须予以忽略,从而保障基金会决策的自主权。新框架明确规定,基金会作为受托人持有的信托财产在法律上独立且与基金会自有财产分离,确保资产隔离的清晰性。争议解决机制也得到了强化,扩大的仲裁条款赋予仲裁庭类似法院的权力,使争议能够高效、保密地解决,并符合国际最佳实践。这些变化是RAK ICC维护前瞻性法律与监管环境整体战略的一部分,旨在满足全球标准的同时兼顾客户群体的特定需求。这也体现了该司法辖区在支持兼顾控制、隐私与长期安全的高端财富规划策略方面的承诺。通过强化其基金会制度,RAK ICC正巩固其在阿联酋的地位,成为寻求安全、灵活且符合国际合规标准的财富保全与跨代规划解决方案的可信赖合作伙伴。关于RAK ICC阿勒哈伊马国际公司注册中心(Ras Al Khaimah International Corporate Centre,简称RAK ICC)是一家总部位于阿联酋阿勒哈伊马的公司注册机构。该机构提供国际商业公司及基金会架构,通常用于私人及商业结构设计、资产整合以及继承规划。截至目前,RAK ICC已注册成立数千家国际公司,并为数十亿迪拉姆的结构化资产提供支持。其服务对象包括高净值人士、企业家及寻求灵活、安全的长期商业与财富管理方案的企业。媒体咨询请联系我们:Phone: +971 7 207 7177Email: info@rakicc.comWebsite: https://www.rakicc.com/contact-us/来源: RAK ICC Copyright 2025 亚太商讯 via SeaPRwire.com.
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RAK ICC以2025年立法升级加强基金会制度 ACN Newswire

RAK ICC以2025年立法升级加强基金会制度

阿联酋拉斯海马市, 2025年8月14日 - (亚太商讯 via SeaPRwire.com) - 阿勒哈伊马国际公司注册中心(RAK ICC)宣布对其2019年《基金会条例》进行重大修订,新规已于2025年7月31日生效。此次修订是该制度自推出以来最为重要的更新之一,进一步巩固了阿联酋作为财富架构与长期资产保护竞争性司法辖区的地位。RAK ICC基金会因其灵活性、保密性及法律稳健性而广受认可,成为阿联酋国内外高净值人士、企业家及家族办公室的首选架构工具。这类结构通常用于继承规划、家族治理,以及将多元化资产整合于单一法律实体之下。2025年的修订引入了更强的法律保障及改进的治理措施,包括:1. 防火墙条款 —— 对与RAK ICC法规相冲突的外国判决提供更强有力的保护。2. 三年诉讼时效 —— 将对基金会设立或资产转移提出异议的时限限制为三年。3. 诉因条款 —— 债权人欺诈索赔仅限于涉案的特定资产,且仅在该行为导致创办人资不抵债时才适用。4. 胁迫与高管保护 —— 宣告在外国法律胁迫下采取的行为无效,从而保障基金会内部治理的自主权。5. 强化仲裁机制 —— 允许通过具备法院级权力的私下仲裁方式解决争议。6. 私人受托基金会条款 —— 明确基金会作为受托人持有财产时的资产隔离及受信义务的完整性。在RAK ICC基金会持有的资产现将享有更强的防火墙保护,确保与阿联酋法律相冲突的外国判决无法对其执行。新规设立了三年的时效期,用于限制对基金会成立或资产转入的质疑,为创办人及受益人提供更大的确定性。改革还收紧了债权人保护规则,在欺诈性转让索赔中须证明创办人资不抵债,并将责任限定在争议资产的价值范围内,以防涉及无关财产。此外,修订后的法规着重维护治理完整性和运营韧性。基金会高管在收到与RAK ICC法律不一致的外国命令时,必须予以忽略,从而保障基金会决策的自主权。新框架明确规定,基金会作为受托人持有的信托财产在法律上独立且与基金会自有财产分离,确保资产隔离的清晰性。争议解决机制也得到了强化,扩大的仲裁条款赋予仲裁庭类似法院的权力,使争议能够高效、保密地解决,并符合国际最佳实践。这些变化是RAK ICC维护前瞻性法律与监管环境整体战略的一部分,旨在满足全球标准的同时兼顾客户群体的特定需求。这也体现了该司法辖区在支持兼顾控制、隐私与长期安全的高端财富规划策略方面的承诺。通过强化其基金会制度,RAK ICC正巩固其在阿联酋的地位,成为寻求安全、灵活且符合国际合规标准的财富保全与跨代规划解决方案的可信赖合作伙伴。关于RAK ICC阿勒哈伊马国际公司注册中心(Ras Al Khaimah International Corporate Centre,简称RAK ICC)是一家总部位于阿联酋阿勒哈伊马的公司注册机构。该机构提供国际商业公司及基金会架构,通常用于私人及商业结构设计、资产整合以及继承规划。截至目前,RAK ICC已注册成立数千家国际公司,并为数十亿迪拉姆的结构化资产提供支持。其服务对象包括高净值人士、企业家及寻求灵活、安全的长期商业与财富管理方案的企业。媒体咨询请联系我们:Phone: +971 7 207 7177Email: info@rakicc.comWebsite: https://www.rakicc.com/contact-us/来源: RAK ICC Copyright 2025 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com
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TANAKA PRECIOUS METAL GROUP宣布将与JEPLAN进行业务合作以实现脱碳与循环型社会 ACN Newswire

TANAKA PRECIOUS METAL GROUP宣布将与JEPLAN进行业务合作以实现脱碳与循环型社会

东京, 2025年8月14日 - (亚太商讯 via SeaPRwire.com) - TANAKA PRECIOUS METAL GROUP Co., Ltd.(总公司:东京都中央区、执行总裁:田中 浩一朗)决定与株式会社JEPLAN(总公司:神奈川县川崎市、代表取缔役 社长兼执行总裁:高尾 正树、以下简称“JEPLAN”) 开展业务合作,以减少TANAKA PRECIOUS METAL TECHNOLOGIES Co., Ltd.在贵金属回收工艺中的CO₂排放,并推进有机物的资源化再利用。本次合作由长期致力于在贵金属领域推动循环经济(Circular Economy)的TANAKA、以及在塑料领域持续精进技术的的JEPLAN携手推动,旨在实现脱碳化和循环型社会的目标。TANAKA迄今为止为实现循环型社会所方面的努力TANAKA自1885年创业以来,作为贵金属行业的领军企业长年致力于稀缺资源贵金属的回收。其中受客户委托回收的工序废弃物中,对于以有机物(塑料)为主要成分、且附着或吸附有贵金属的工序废弃物,一直以来通过烧成工艺去除有机物,并从剩余的灰烬中回收贵金属。尽管这种烧成处理方式能够有效去除环境管制物质,但在去除过程中有机物燃烧所产生的CO₂排放,成为实现脱碳社会的课题。通过与JEPLAN业务合作、革新贵金属回收工艺JEPLAN已建立了针对聚对苯二甲酸乙二醇酯(PET,一种塑料)的创新化学回收技术。为了解决上述CO₂排放量的课题,TANAKA通过与JEPLAN的业务合作,除了传统的采用烧成的贵金属回收工艺以外,还在考虑未来利用化学回收处理的工艺。预期的化学回收处理的对象为注射器、擦拭布等塑料。预计通过该技术,贵金属回收工艺中的CO₂排放量可控制在以往的10%左右。此外,该新工艺不仅可以回收贵金属,也可以实现塑料再生,TANAKA与JEPLAN将充分发挥各自在专业领域的优势,共同为实现脱碳和循环型社会贡献力量。 株式会社JEPLAN总公司所在地:神奈川县川崎市川崎区扇町12-2成立:2007年1月代表人:代表取缔役 社长兼执行总裁 高尾 正树主要业务内容:PET化学回收技术相关业务(对象:PET塑料瓶、聚酯)等官方 HP:http://www.jeplan.co.jpJEPLAN集团以“循环一切”为使命,致力于实现循环经济。通过使用创新的PET化学回收技术,将废弃PET(PET塑料瓶、聚酯纤维等)分解至分子水平并去除杂质,使其重新生成与石油基材料同等品质的再生材料。通过使用这项创新技术致力于回收再利用,实现有限资源的循环,并为减少CO₂排放量做出贡献。关于TANAKATANAKA自1885 年(明治18年)创业以来,营业范围以贵金属为中心,并以此展开广泛活动。公司在日本国内拥有非常可观的贵金属交易量, 长年以来不遗余力地进行工业用贵金属制品的制造和销售,以及提供作为宝石饰品及资产的贵金属商品。并且,作为贵金属相关的专家集团,日本国内外的各集团公司进行制造、销售以及技术一体化,携手合作提供产品及服务。2024年度(截至2024年12月)集团总营业额为8,469亿日元,拥有5,591名员工。产业事业全球网站https://www.tanaka.com.cn产品咨询表TANAKA PRECIOUS METAL TECHNOLOGIES Co., Ltd.https://www.tanaka.com.cn/inquiries-on-industrial-products/新闻媒体咨询处TANAKA PRECIOUS METAL GROUP Co., Ltd.https://www.tanaka.com.cn/inquiries-for-media/新闻稿: https://www.acnnewswire.com/docs/files/20250814_CN.pdf Copyright 2025 亚太商讯 via SeaPRwire.com.
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