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SUBANG JAYA, Malaysia, March 10, 2025 /PRNewswire/ -- Sunway Medical Centre, Sunway City (SMC) has yet again ranked in the top 250 hospitals globally in the latest Newsweek's World's Best Hospitals 2025 rankings. (from left) Dato Lau Beng Long, President, Sunway Healthcare Group (SHG); Dr Khoo Chow Huat, Managing Director, Hospital & Healthcare Operations, SHG; Dr Seow Vei Ken, Chief Executive Officer, Sunway Medical Centre, Sunway City (SMC); Dr Low Kwai Siong, Medical Director, SMC; and Tan Mei Shin, Senior Director, Business Development and Corporate Communications, SMC Honoured for the second consecutive year, SMC improved from rank 233rd in 2024 to rank 193rd in 2025, and also is the top hospital in Malaysia in the latest listing. The rankings list top 250 hospitals globally from 30 countries based on a comprehensive survey that gathered insights from medical experts, patient surveys, hospital quality metrics, and Statista Patient-Reported Outcome Measures (PROMs) Implementation Survey. Dato' Lau Beng Long, President of Sunway Healthcare Group remarked, "As the flagship hospital of Sunway Healthcare Group, SMC takes pride in its commitment to excellence in healthcare and hospitality in driving us to this level of international recognition. Being ranked among the top 250 hospitals globally, with the likes of the Mayo Clinic, The John Hopkins Hospital, Singapore General Hospital, and The University of Tokyo Hospital for two consecutive years is a testament to the unwavering dedication of our team especially medical specialists, nurses and allied health professionals." "We are proud to lead the way in Malaysia, and this achievement reaffirms our aim to provide the highest level of clinical care and to continue elevating the overall healthcare status in the country." The latest accomplishment builds upon SMC's recent success in Newsweek's Asia's Top Private Hospitals 2025 ranking, where it was ranked 2nd in Asia for cataract surgery, and 3rd in Asia for refractive eye surgery, while also featured in the top 10 of Asia's ranking for hip surgery and hip replacement (6th); knee surgery and knee replacement (6th); and shoulder surgery (10th). The hospital was also featured in Newsweek's Best Specialist Hospitals Asia Pacific list for 2023 and 2024. Dato' Lau also made history as the first Malaysian healthcare leader to be inducted in Newsweek's Top Hospital CEOs 2024 list, alongside other prominent CEOs from the globe's leading medical facilities. As Malaysia's largest private quaternary hospital, SMC is the first hospital in Malaysia to achieve three major hospital-wide accreditations: Joint Commission International (JCI) Accreditation, The Gold Seal of Approval from the United States; the Australian Council on Healthcare Standards (ACHS); and the Malaysian Society for Quality in Health (MSQH).
Prospective study finds Lunit AI increases cancer detection by 13.8% in single-reader settings without raising recall rates, presenting a game-changing tool for countries relying on single-reader mammography screening SEOUL, South Korea, March 10, 2025 /PRNewswire/ -- Lunit (KRX:328130.KQ), a leading provider of AI-powered solutions for cancer diagnostics and therapeutics, today announced the publication of a groundbreaking prospective study in Nature Communications validating the real-world effectiveness of AI-powered mammography screening in South Korea's national breast cancer screening program. Conducted as the world's first large-scale, multicenter prospective study in a single-reading setting, the research underscores how AI-assisted mammography interpretation significantly improves breast cancer detection rates without increasing recall rates. Lunit's AI-powered mammography analysis solution, Lunit INSIGHT MMG The study was led by Professor Yun-Woo Chang from Soonchunhyang University Seoul Hospital, in collaboration with both breast and general radiologists from six leading academic hospitals in South Korea. The study analyzed 24,543 women aged 40 and above who underwent routine biennial mammography (2D full-field digital mammogram) between February 2021 and December 2022 as part of Korea's national breast cancer screening program. The study compared the performance of breast radiologists interpreting screening mammograms with and without Lunit's AI-based computer-aided detection, Lunit INSIGHT MMG. The results revealed that AI-assisted breast radiologists detected 13.8% more screen-detected breast cancers than those relying solely on conventional interpretation methods, or without AI assistance. The cancer detection rate (CDR) increased from 5.01 (per 1,000) to 5.70 with AI assistance, while recall rates (RRs) remained statistically unchanged, ensuring improved clinical effectiveness and minimizing unnecessary additional recalls. Moreover, AI assistance led to a significant improvement in detecting small-sized tumors and node-negative cancers, key indicators of improved early detection. Additionally, the study evaluated Lunit INSIGHT MMG's impact on general radiologists who do not specialize in breast imaging through a simulated retrospective study. The results demonstrated that AI assistance led to an even greater improvement in CDRs for general radiologists, with an increase of 26.4% (3.87 to 4.89 per 1,000), underscoring AI's potential to support radiologists with varying levels of expertise. "This prospective study offers compelling real-world evidence that AI can improve early cancer detection while maintaining effectiveness and reducing unnecessary patient anxiety caused by false positives in a single-reading setting," said Professor Chang, the lead and corresponding author of the study. A Proven Solution for Single and Double-Reading Screening Systems The publication further builds upon Lunit INSIGHT MMG's well-established track record in improving breast cancer detection. In Sweden, Capio St. Göran Hospital conducted a prospective clinical trial to assess Lunit AI's effectiveness in breast cancer screening when replacing one reader within a double-reading setting. Following positive trial results, Capio St. Göran Hospital became the world's first to replace one of two radiologists in its double-reading workflow with AI, marking a paradigm shift in breast cancer screening. "This latest prospective study in South Korea further solidifies Lunit INSIGHT MMG's potential as an indispensable tool in breast cancer screening," said Brandon Suh, CEO of Lunit. "Whether in a single-reader or double-reader setting, AI can serve as a powerful force multiplier, assisting radiologists in detecting cancer earlier and more accurately." Shaping the Future of National Breast Cancer Screening Programs With mounting evidence supporting AI's role in breast cancer screening, Lunit is driving its global adoption. Lunit INSIGHT MMG has already been deployed in national breast screening programs in Australia, Sweden, Iceland, Singapore, Saudi Arabia, and Qatar, helping healthcare systems enhance efficiency and optimize diagnostic accuracy. The study's findings are expected to influence global breast cancer screening protocols, particularly in countries where single-reading mammography interpretation is widely practiced. By demonstrating AI's ability to enhance radiologists' accuracy without increasing RRs, the study provides critical data supporting AI's role in optimizing cancer detection while reducing the workload burden on radiologists. This is particularly relevant as many countries face a shortage of specialized breast imaging professionals, making AI an important tool to improve efficiency and maintain high diagnostic standards. "As AI adoption accelerates, we remain committed to driving innovation and making AI-powered cancer screening the new standard of care," added Suh. "By working closely with healthcare providers worldwide, we aim to ensure that AI benefits as many patients as possible." About Lunit Founded in 2013, Lunit (KRX:328130.KQ) is a medical AI company on a mission to conquer cancer. Lunit harnesses AI-powered medical image analytics and biomarker analysis to ensure accurate diagnosis and optimal treatment for each cancer patient. The FDA-cleared Lunit INSIGHT suite for cancer screening serves over 4,800 medical institutions across 55+ countries. Lunit clinical studies have been published in top journals, including the Journal of Clinical Oncology and the Lancet Digital Health, and presented at global conferences such as the ASCO and RSNA. Headquartered in Seoul, South Korea, with a network of offices worldwide, Lunit leads the global fight against cancer. Discover more at lunit.io.
HONG KONG, March 10, 2025 /PRNewswire/ -- On March 5, during the 2025 Mobile World Congress (MWC25), the 5G UAV medical delivery network solution jointly developed by China Telecom, Hangzhou Antwork Network Technology and Zhejiang University was awarded the Global Mobile Award (GLOMO Award) for "Best Mobile Innovation for Connected Health and Wellbeing." This groundbreaking achievement signifies that the integration of "5G + low-altitude + healthcare" is poised to enter the stage of large-scale application, opening up new pathways for the equitable distribution of medical resources worldwide. China Telecom, driven by deep insights into the pain points of the healthcare industry and a forward-looking strategic layout, has taken the lead in constructing a 5G-A technology matrix. To address issues such as low efficiency in medical supply delivery and regional resource imbalances, the company has innovatively introduced 5G-A super terrestrial and aerial integration technology alongside a high-precision medical sensing network. This creates a low-altitude medical corridor that is extensive, responsive, and secure. The technology employs a combination of high and low frequencies, using dynamic resource scheduling through smart beamforming in urban areas. In suburban regions, it utilizes new wide-angle power-sharing smart antennas for broad coverage, overcoming geographical limitations. Equipped with perception AS, perception SF, and base station sensing devices, the system enables UAV trajectory tracking, electronic fence protection, and real-time monitoring of multiple targets to ensure flight safety. It supports low-altitude network high-definition video transmission and, combined with UAVs capable of withstanding winds over level 5, significantly enhances transportation efficiency, providing 24-hour immediate response for emergency medical scenarios. Currently, this solution is being piloted in Zhejiang Province. The use of UAV delivery routes for blood transport has significantly reduced transportation time compared to ground logistics, effectively meeting both "emergency blood use" and "planned blood replenishment" needs, thereby greatly enhancing emergency response speed. By leveraging UAVs as a "highway" for rural areas, an aerial bridge has been established between central hospitals and grassroots health clinics, facilitating the implementation of a tiered healthcare system and allowing for more balanced resource allocation. According to actual flight data, a single UAV flight can meet the emergency blood needs of 1-2 patients, benefiting remote areas with weaker healthcare resources and increasingly demonstrating its social impact. The success of the 5G-A smart healthcare solution exemplifies the deep integration of "terrestrial and aerial fusion" technology with medical scenarios. UAV medical delivery represents not only a technological breakthrough but also a new paradigm in life-saving operations. In the future, China Telecom will continue to collaborate with partners across the industry chain to further unlock the limitless potential of 5G-A. This initiative aims to catalyze a transformative increase in the overall productivity of vertical industries, injecting new qualitative productivity into the high-quality development of the digital economy. The Global Mobile Awards (GLOMO), founded by the authoritative organization GSMA in 1996, features a judging panel of over 260 analysts, media representatives, and industry experts as of 2025. It is the most prestigious award in the telecommunications industry, often referred to as the "Oscars of Mobile Communication." The GLOMO Awards aims to recognize individuals and companies that drive innovation and demonstrate exceptional achievements in the rapidly growing mobile sector.
HONG KONG, March 10, 2025 /PRNewswire/ -- AIM Vaccine Co., Ltd. (06660.HK), a leading PRC vaccine company, published an announcement on March 9, 2025, the company's research and development of a diploid rabies vaccine has recently received the Clinical Trial Approval Notice from the National Medical Products Administration. This product is an upgraded version of the diploid rabies vaccine, featuring significantly high efficacy, marking a major iterative upgrade in the global rabies vaccine technology field. Animal trials have shown that the vaccine generates antibodies that provide a high level of protection, with efficacy significantly surpassing that of already marketed diploid rabies vaccines under the same dosage conditions. This vaccine has successfully overcome the technical bottlenecks of traditional processes, which are characterized by low virus titer and low yield. Optimizations and innovations have been made in the purification process, resulting in significant improvements in product quality and safety. It can be administered using a five-injection method, a simplified four-injection method, or a 2-1-1 four-injection method, offering more flexibility and convenience. Since February, AIM Vaccine has made several breakthrough advancements that highlight its innovative capabilities and global strategy. Its mRNA RSV (Respiratory Syncytial Virus) vaccine has received clinical approval in the U.S., and the company announced a comprehensive deployment of the DeepSeek large model, realizing a strategic upgrade to an "AI + Smart Vaccine Enterprise." In the context of major global investment banks raising target prices for Chinese assets, biotech stocks with high technological innovation content are expected to encounter significant opportunities. China Galaxy International Securities[1] believes that the pharmaceutical sector will undergo a recovery, and structural opportunities still exist. From the perspective of short-term and medium-to-long-term growth certainty, it is optimistic about the innovative pharmaceutical supply chain, international expansion, and leading companies in niche sectors. Fosun International Securities[2] previously pointed out that AIM's innovative products are driving a revaluation of its value. Considering AIM Vaccine's strong R&D capabilities, technological leadership, and international market expansion potential, it has assigned a "Buy" rating with a target price of HKD 11. Note 1: http://www.aastocks.com/tc/stocks/analysis/china-hot-topic-content.aspx?id=GLH1848484L&catg=1&source=GLH Note 2: http://www.aastocks.com/tc/stocks/news/glh-news/GLH1832345L/1
OMLYCLO® (omalizumab-igec) is the first and only omalizumab biosimilar approved by the FDA Regulatory approval for interchangeability was supported by positive phase III data demonstrating comparable efficacy and safety profile with the reference product XOLAIR® (omalizumab)[1] The availability of the first omalizumab biosimilar will help increase access and potentially lower the healthcare cost for people with asthma and allergic diseases JERSEY CITY, N.J., March 10, 2025 /PRNewswire/ -- Celltrion today announced the U.S. Food and Drug Administration (FDA) approved OMLYCLO® (omalizumab-igec) as the first and only biosimilar designated as interchangeable with XOLAIR® (omalizumab) for the treatment of moderate to severe persistent asthma, chronic rhinosinusitis with nasal polyps (CRSwNP), Immunoglobulin E (IgE)-mediated food allergy, and chronic spontaneous urticaria (CSU).[2] "We are proud to achieve the approval of the first biosimilar to omalizumab in the U.S., which will help broaden access to this important medicine for patients with allergic and respiratory conditions, as well as for physicians, payers and providers," said Hetal Patel, Vice President of Medical Affairs at Celltrion USA. "The interchangeability designation of OMLYCLO reinforces confidence among physicians and patients that there is no decrease in effectiveness or increase in safety risk associated with switching between OMLYCLO and the reference product." The FDA approval and designation of interchangeability are based on comprehensive clinical evidence, including results from a global Phase III clinical trial involving 619 adult patients with CSU up to Week 40. Patients were randomized to receive 300 mg or 150 mg of OMLYCLO or reference product every 4 weeks. From Week 12, patients who received OMLYCLO were continued on OMLYCLO, and patients who received 300mg of the reference product were re-randomized in a 1:1 ratio to switch to OMLYCLO or to continue reference product. From Week 24, patients were followed up until Week 40 without dosing. The result demonstrated the comparable efficacy and safety of OMLYCLO to reference product during both treatment and off-dose periods.[1] An interchangeable biosimilar is a biosimilar that meets additional requirements outlined by the law that allows for the FDA to approve biosimilar and interchangeable biosimilar medications.[3] "The approval of OMLYCLO could have a meaningful impact for the medical community and patients, offering a high quality and affordable treatment option, while reducing the burden of healthcare costs," said Thomas Nusbickel, Chief Commercial Officer at Celltrion USA. "With our integrated development, manufacturing, and commercialization platform, Celltrion remains committed to alleviating treatment costs and delivering life-changing medicines to support patients with allergic conditions in the U.S." About OMLYCLO® (omalizumab-igec) OMLYCLO® (omalizumab-igec) is the first U.S. Food and Drug Administration (FDA)-approved anti-IgE antibody biosimilar referencing XOLAIR® (omalizumab). OMLYCLO 75 mg/0.5 mL and 150 mg/mL solution in a single-dose prefilled syringe is approved as interchangeable with reference product for all indications based on comprehensive data and clinical evidence confirming the therapeutic equivalence to XOLAIR.[1],[2] OMLYCLO was also approved by the European Commission (EC) in May 2024. INDICATION OMLYCLO® (omalizumab-igec) injection, is an anti-IgE antibody indicated for: Moderate to severe persistent asthma in adults and pediatric patients ≥6 years of age with a positive skin test or in vitro reactivity to a perennial aeroallergen and symptoms that are inadequately controlled with inhaled corticosteroids Chronic rhinosinusitis with nasal polyps (CRSwNP) in adult patients ≥18 years of age with inadequate response to nasal corticosteroids, as add-on maintenance treatment IgE-mediated food allergy in adult and pediatric patients aged ≥1 year age for the reduction of allergic reactions (Type I), including anaphylaxis, that may occur with accidental exposure to one or more foods. To be used in conjunction with food allergen avoidance Chronic spontaneous urticaria (CSU) in adults and adolescents ≥12 years of age who remain symptomatic despite H1 antihistamine treatment Limitations of Use: Not indicated for: acute bronchospasm or status asthmaticus; emergency treatment of allergic reactions, including anaphylaxis; other forms of urticaria. IMPORTANT SAFETY INFORMATION WARNING: ANAPHYLAXIS Anaphylaxis presenting as bronchospasm, hypotension, syncope, urticaria, and/or angioedema of the throat or tongue, has been reported to occur after administration of omalizumab products. Anaphylaxis has occurred as early as after the first dose of omalizumab products, but also has occurred beyond 1 year after beginning regularly administered treatment. Because of the risk of anaphylaxis, initiate OMLYCLO therapy in a healthcare setting and closely observe patients for an appropriate period of time after OMLYCLO administration. Health care providers administering OMLYCLO should be prepared to manage anaphylaxis which can be life-threatening. Inform patients of the signs and symptoms of anaphylaxis and instruct them to seek immediate medical care should symptoms occur. Selection of patients for self-administration of OMLYCLO should be based on criteria to mitigate risk from anaphylaxis. Contraindications: Severe hypersensitivity reaction to OMLYCLO or any ingredient of OMLYCLO. Anaphylaxis. Omalizumab products, including OMLYCLO, have been associated with anaphylaxis, reported in both clinical trials and postmarketing data. Patients with a history of anaphylaxis to foods, medications, or other causes face an increased risk. Initiate OMLYCLO only in a healthcare setting with anaphylaxis management capabilities. Patients should be monitored for an appropriate period post-administration, informed of symptoms, and instructed to seek immediate medical care if they occur. Malignancy. Malignancies have been observed in clinical studies, with various cancer types reported. The long-term risk, especially in high-risk groups, is unknown. Acute Asthma Symptoms and Deteriorating Disease. Omalizumab products have not been shown to alleviate asthma exacerbations acutely. Do not use OMLYCLO to treat acute bronchospasm or status asthmaticus. Corticosteroid Reduction. Do not discontinue systemic or inhaled corticosteroids abruptly upon initiation of OMLYCLO therapy for asthma or CRSwNP. Eosinophilic Conditions. Be alert to eosinophilia, vasculitic rash, worsening pulmonary symptoms, cardiac complications, and/or neuropathy, especially upon reduction of oral corticosteroids. Fever, Arthralgia, and Rash. Stop OMLYCLO if a patient develops this constellation of signs and symptoms, including arthritis/arthralgia, rash, fever, and lymphadenopathy. Parasitic (Helminth) Infection. Monitor patients at high risk of geohelminth infection while on OMLYCLO therapy. Laboratory Tests. Omalizumab increases serum total IgE due to drug:IgE complexes. Do not use serum total IgE levels within one year of discontinuation to reassess dosing regimen, as they may not reflect steady-state free IgE. Potential Medication Error Related to Emergency Treatment of Anaphylaxis. OMLYCLO should not be used for the emergency treatment of allergic reactions, including anaphylaxis. Instruct patients that OMLYCLO is for maintenance use to reduce allergic reactions, including anaphylaxis, while avoiding food allergens. Most Common Adverse Reactions Asthma: In patients ≥12 years, reported in ≥1%: arthralgia, general pain, leg pain, fatigue, dizziness, fracture, arm pain, pruritus, dermatitis, and earache. In pediatric patients (6 to <12 years), reported in ≥3%: nasopharyngitis, headache, pyrexia, upper abdominal pain, streptococcal pharyngitis, otitis media, viral gastroenteritis, arthropod bites, and epistaxis. CRSwNP: In ≥3% of adults: headache, injection site reactions, arthralgia, upper abdominal pain, and dizziness. IgE-Mediated Food Allergy: In ≥3% of patients: injection site reactions and pyrexia. CSU: In ≥2% of patients: nausea, nasopharyngitis, sinusitis, upper respiratory tract infections (viral and non-viral), arthralgia, headache, and cough. For more information, see Full Prescribing Information. About Celltrion Celltrion is a leading biopharmaceutical company that specializes in researching, developing, manufacturing, marketing and sales of innovative therapeutics that improve people's lives worldwide. Celltrion is a pioneer in the biosimilar space, having launched the world's first monoclonal antibody biosimilar. Our global pharmaceutical portfolio addresses a range of therapeutic areas including immunology, oncology, hematology, ophthalmology and endocrinology. Beyond biosimilar products, we are committed to advancing our pipeline with novel drugs to push the boundaries of scientific innovation and deliver quality medicines. For more information, please visit our website www.celltrion.com/en-us. and stay updated with our latest news and events on our social media: LinkedIn, Instagram, X, and Facebook. About Celltrion USA Celltrion USA is Celltrion's U.S. subsidiary established in 2018. Headquartered in New Jersey, Celltrion USA is committed to expanding access to innovative biologics to improve care for U.S. patients. Celltrion currently has nine biosimilar products approved by the U.S. FDA: INFLECTRA® (infliximab-dyyb), TRUXIMA® (rituximab-abbs), HERZUMA® (trastuzumab-pkrb), VEGZELMA® (bevacizumab-adcd), YUFLYMA®(adalimumab-aaty), AVTOZMA® (tocilizumab-anho), STEQEYMA® (Ustekinumab-stba) STOBOCLO® (denosumab-bmwo) and OSENVELT® (denosumab-bmwo) as well as a novel biologic ZYMFENTRA® (infliximab-dyyb). Celltrion USA will continue to leverage Celltrion's unique heritage in biotechnology, supply chain excellence and best-in-class sales capabilities to improve access to high-quality biopharmaceuticals for U.S. patients. For more information, please visit www.celltrionusa.com, and stay updated with our latest news and events on our social media: LinkedIn. FORWARD-LOOKING STATEMENT Certain information set forth in this press release contains statements related to our future business and financial performance and future events or developments involving Celltrion Inc. and its subsidiaries that may constitute forward-looking statements, under pertinent securities laws. These statements may be also identified by words such as "prepares", "hopes to", "upcoming", "plans to", "aims to", "to be launched", "is preparing", "once gained", "could", "with the aim of", "may", "once identified", "will", "working towards", "is due", "become available", "has potential to", the negative of these words or such other variations thereon or comparable terminology. In addition, our representatives may make oral forward-looking statements. Such statements are based on the current expectations and certain assumptions of Celltrion Inc. and its subsidiaries' management, of which many are beyond its control. Forward-looking statements are provided to allow potential investors the opportunity to understand management's beliefs and opinions in respect to the future so that they may use such beliefs and opinions as one factor in evaluating an investment. These statements are not guarantees of future performance and undue reliance should not be placed on them. Such forward-looking statements necessarily involve known and unknown risks and uncertainties associated with the company's business, including the risk factors disclosed in its Annual Report and/or Quarterly Reports, which may cause actual performance and financial results in future periods to differ materially from any projections of future performance or results expressed or implied by such statements. Celltrion Inc. and its subsidiaries undertake no obligation to update forward-looking statements if circumstances or management's estimates or opinions should change except as required by applicable securities laws. Trademarks OMLYCLO® is a registered trademark of CELLTRION, Inc.XOLAIR® is a registered trademark of Novartis AG. References [1] Sarbjit Singh Saini et al., CT-P39 Compared With Reference Omalizumab in Chronic Spontaneous Urticaria: Results From a Double-Blind, Randomized, Active-Controlled, Phase 3 Study. Available at: https://onlinelibrary.wiley.com/doi/pdf/10.1111/all.16446?msockid=30d535870b30638b14c920090a18627c [Last accessed March 2025] [2] OMLYCLO U.S. prescribing information (2025) [3] U.S. Food and Drug Administration (FDA). Available at: https://www.fda.gov/drugs/things-know-about/9-things-know-about-biosimilars-and-interchangeable-biosimilars [Last accessed March 2025] US-OML-25-00001 For further information please contact: Andria Arenaaarena@jpa.com+1 516-578-0057
Histotripsy is an FDA-approved technology that offers liver cancer patients a non-invasive, painless, and highly effective treatment option HONG KONG, March 7, 2025 /PRNewswire/ -- Manulife announced today the extension of its strategic partnership with CUHK Medical Centre (CUHKMC), originally established in 2021, as part of its commitment to enhancing access to quality healthcare for its customers. Manulife is pleased to share that, through its Holistic "Medical Professional Support Service" for specified medical insurance plan[1] customers diagnosed with cancer or suspected of having cancer, it will incorporate histotripsy as a treatment option, once this treatment becomes publicly available at CUHKMC, and patients would be enrolled in clinical trials for close monitoring and evaluation of the clinical outcome. Liver cancer is the fifth most common cancer in Hong Kong, making up 4.6% of all new cancer cases in 2022.[2] Histotripsy is an FDA-approved technology that offers liver cancer patients a non-invasive, painless, and highly effective treatment option.[3] Earlier, this treatment was introduced to medical institutions in Hong Kong through donations from the Li Ka Shing Foundation. [3] "This extended partnership highlights Manulife's commitment to being a pioneering health insurance provider in Hong Kong, supporting our customers throughout their health journeys and helping to protect more lives," said Carrie Tong, Chief Operations Officer of Manulife Hong Kong and Macau. All Manulife medical plan customers are eligible for coverage of this innovative and FDA-approved histotripsy treatment, further underscoring Manulife's dedication to enhancing the quality of healthcare accessible to customers. Manulife established a strategic partnership with CUHKMC in 2021, providing eligible customers with priority access to the hospital's oncologists for a one-time, free independent medical consultation. In 2023, this partnership was expanded to offer a cashless pre-approval service for over 300 all-inclusive hospital packages, including endoscopic and surgical procedures provided by CUHKMC. Manulife has extended its strategic partnership with CUHK Medical Centre to incorporate histotripsy into its holistic “Medical Professional Support Service”. About Manulife Hong Kong Manulife Hong Kong has been a trusted name for more than 125 years. Since our operations started in Asia in 1897, we have grown to become one of the top-tier providers of financial services, offering a diverse range of protection and wealth products and services to over 2.6 million customers in Hong Kong and Macau. We are committed to helping make decisions easier and lives better for our customers. Manulife Hong Kong, through Manulife International Holdings Limited, owns Manulife (International) Limited, Manulife Investment Management (Hong Kong) Limited, and Manulife Provident Funds Trust Company Limited. These entities are all subsidiaries of Manulife Financial Corporation. About Manulife Manulife Financial Corporation is a leading international financial services provider, helping our customers make their decisions easier and lives better. With our global headquarters in Toronto, Canada, we operate as Manulife across Canada, Asia, and Europe, and primarily as John Hancock in the United States, providing financial advice and insurance for individuals, groups and businesses. Through Manulife Wealth & Asset Management, we offer global investment, financial advice, and retirement plan services to individuals, institutions, and retirement plan members worldwide. At the end of 2024, we had more than 37,000 employees, over 109,000 agents, and thousands of distribution partners, serving over 36 million customers. We trade as 'MFC' on the Toronto, New York, and the Philippine stock exchanges, and under '945' in Hong Kong. Not all offerings are available in all jurisdictions. For additional information, please visit manulife.com. [1] Terms and conditions apply. Eligibility to Holistic "Medical Professional Support Service" applies to customers of Manulife Supreme VHIS Flexi Plan, Manulife Supreme Lite VHIS Supplementary Benefit, Manulife Supreme Medical Plan, Manulife Supreme Lite Medical Supplementary Benefit, ManuMaster Healthcare Series/Benefit, and ManuShine Healthcare Series/Benefit. The content of this press release does not contain all the terms and conditions of policies, and the full terms and conditions are set out in the policy documents. ManuMaster Healthcare Series/Benefit and ManuShine Healthcare Series/Benefit are available as basic plans or supplementary benefits. [2] Figures from the Centre for Health Protection under the HKSAR Department of Health. [3] "Li Ka Shing Foundation funds non-invasive liver cancer treatment for Hong Kong patients" (SCMP, Aug 27, 2024)
Medical/Pharmaceuticals
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