Home Blog Page 2008

VISTA BRINGS XO TO ASIA, STRENGTHENING FLYING SOLUTIONS AMID CONTINUED DEMAND FOR VISTAJET

HONG KONG and SINGAPORE, Oct. 30, 2025 /PRNewswire/ — Vista, the world’s leading private aviation group, announced its 2026 commitment and expansion plans for Asia, along with the outstanding demand for flying solutions through its leading brands VistaJet and XO in the Asia Pacific region during the first half of 2025.

Building excellence in Asia’s evolving aviation landscape

Demand for private flying across Asia Pacific has increased in the first six months of the year, with the company achieving a 26% year-on-year increase in its Program subscription membership in the region. Hong Kong and Singapore remain top destinations in Asia, serving as the main international gateways for North Asia and Southeast Asia respectively, while Kuala Lumpur and Tokyo continue to be popular for both business and leisure travel.

“One of the key drivers behind the strong demand is that these cities cater to both business and leisure travel. They are not only major commercial hubs in Asia, but also highly popular tourist destinations,” says Ian Moore, Chief Commercial Officer at Vista. “We are seeing a clear trend among entrepreneurs and senior executives toward ‘bleisure travel,’ combining work commitments with vacation time. Particularly with high net-worth individuals, the line between business and private time is increasingly blurred, as they often travel with family members.”

Vista brings XO to Asia, strengthening flying solutions amid continued demand for VistaJet
Vista brings XO to Asia, strengthening flying solutions amid continued demand for VistaJet

XO, Vista’s digital marketplace offers flexible, on demand jet access

XO is a global private aviation network, providing flexible, efficient and immediate access to more than 2,000 aircraft around the world. It secures the right aircraft for every private flight across all cabin classes — from short domestic hops to international, multi-leg itineraries.

While North America remains the leading market for the brand, international flights booked with XO surged nearly 40% in 2024. This remarkable growth highlights the increasing demand for transparent, flexible private aviation solutions in both emerging and established markets.

“We are seeing increasing demand from clients in Asia who are seeking flexible and instant flight solutions. Through the XO mobile application, Asian clients may book and confirm their flights with real-time pricing,” shares Crystal Wong, President — Asia Pacific at Vista. “It is the simplest and most flexible way to begin flying privately.”

VistaJet’s continued growth in Asia

VistaJet has been a leader in Asia Pacific’s private aviation market for 17 years. VistaJet solutions replicate the experience of aircraft ownership without the complexities or associated costs, by providing Members guaranteed access to its iconic fleet of silver and red aircraft, ensuring the highest standard of safety and service for seamless global travel, 365 days a year.

In the first half of 2025, Program membership grew by 26% year-on-year growth in. Japan set a record as the fastest growing region, achieving a 67% increase, followed by Singapore with a growth of 50%.

This exceptional performance is underpinned by strong economic momentum across the Asia Pacific region. Amid shifting geopolitical landscape, Vista recognizes the importance of forging long-lasting relationships both regionally and globally. With Asia’s outward-looking economies and emerging regional superpowers, the region presents a compelling proposition for international collaboration and growth.

Corporations increasingly turn to business jets to maximize time savings and enable executives to work efficiently and in privacy while in the air. This is made possible by the ample space and amenities exclusive to business jets, such as Vista’s flagship Global 7500 aircraft.

As the largest and longest-range business jet, the Global 7500 offers unbeatable connectivity flying up to 17 hours non-stop. Precision-engineered wings provide an exceptionally smooth ride in the large cabin, with four separate living spaces, including a permanent bedroom, perfectly suited for a business or family dynamic.

“With XO now in Asia, our clients enjoy the best of both worlds through Vista’s global infrastructure, from on demand flights with instant booking through the XO marketplace to a guaranteed flight solution that replicates an aircraft ownership experience with VistaJet. We deliver seamless travel that combines international reach, domestic flexibility and bespoke lifestyle experiences,” concludes Ian Moore, Chief Commercial Officer of Vista.

About Vista

Vista Global Holding Limited (Vista) is the world’s leading global business aviation company providing worldwide business flight services through its network of subsidiaries and a team of over 4,000 experts. A global group headquartered in Dubai, Vista integrates a unique portfolio of companies to offer asset free services to cover all key aspects of business aviation, including guaranteed and on demand global flight coverage, subscription and membership solutions, and trading and management services.

Innovating the industry for 20 years through continuous investment in talent, technology, and infrastructure, Vista’s mission is to provide the most advanced flying services at the very best value — anytime, anywhere around the world.

Vista’s extensive industry expertise enables it to deliver comprehensive end-to-end solutions and technology to meet the needs of business aviation clients around the world. These services are offered through its leading brands, including VistaJet and XO.

More Vista information and news at www.vistaglobal.com.

“Vista” is a trade name for Vista Global Holding Limited. Vista does not operate any aircraft. All flights are performed by properly licensed operators, which may include subsidiaries such as VistaJet Limited or VistaJet GmbH. Vista also holds a non-controlling minority stake in FAA-licensed and DOT registered US direct air carriers Western Air Charter, Inc. (DBA Vista America), Jet Select, LLC (DBA Vista America), and Talon Air LLC.

Information:
press@vistaglobal.com 

 

Hong Kong Country Club Elevates City’s Tennis Scene: ITF World Masters Tour MT700

HONG KONG, Oct. 30, 2025 /PRNewswire/ — Sanctioned by the International Tennis Federation (ITF) and hosted in partnership with the Hong Kong, China Veterans’ Tennis Association and the Hong Kong, China Tennis Association (HKCTA), the Country Club ITF World Tennis Masters Tour 2025 will take place at the Hong Kong Country Club from 27 October to 9 November 2025.

Besides the world-class tennis action, the ITF World Masters Tennis Community Event was also held at the Hong Kong Country Club, featuring two tennis clinics led by Australian Glenn Busby, former ITF world champion and current Men’s 65+ singles No. 1. The clinics were aimed at inspiring young local players and disabled athletes across Hong Kong as part of the Hong Kong Country Club’s community outreach programme, designed to make tennis more accessible and to nurture the next generation of athletes in Hong Kong.    Busby said, “I’m delighted to be in Hong Kong and have already experienced the spectacular evening harbour view and sampled some of the amazing cuisine. I particularly enjoyed meeting local wheelchair athletes at Sunday’s clinic; the energy and enthusiasm were inspiring. I’m looking forward to competing at the Hong Kong Country Club.”
Besides the world-class tennis action, the ITF World Masters Tennis Community Event was also held at the Hong Kong Country Club, featuring two tennis clinics led by Australian Glenn Busby, former ITF world champion and current Men’s 65+ singles No. 1. The clinics were aimed at inspiring young local players and disabled athletes across Hong Kong as part of the Hong Kong Country Club’s community outreach programme, designed to make tennis more accessible and to nurture the next generation of athletes in Hong Kong. Busby said, “I’m delighted to be in Hong Kong and have already experienced the spectacular evening harbour view and sampled some of the amazing cuisine. I particularly enjoyed meeting local wheelchair athletes at Sunday’s clinic; the energy and enthusiasm were inspiring. I’m looking forward to competing at the Hong Kong Country Club.”

Since 2018, the Hong Kong Country Club has proudly supported the ITF World Tennis Masters Tour The tournament was recently elevated from MT400 status to MT700, and is one of only four MT700 events across Asia, marking a historic milestone as the highest-graded senior tennis tournament ever held in Hong Kong. The elevation highlights both the tournament’s international prestige and Hong Kong’s growing status as a global sporting hub, attracting elite masters-level players (aged 45 to 75+) from around the world, providing a competitive platform to challenge each other and compete for a total prize pool of $504,000 HKD.

Besides the world-class tennis action, the ITF World Masters Tennis Community Event was also held at the Hong Kong Country Club, featuring two tennis clinics led by Australian Glenn Busby, former ITF world champion and current Men’s 65+ singles No. 1. The clinics were aimed at inspiring young local players and disabled athletes across Hong Kong as part of the Hong Kong Country Club’s community outreach programme, designed to make tennis more accessible and to nurture the next generation of athletes in Hong Kong.

Mrs Delaine Chan, Vice Chairman of the Hong Kong Country Club, expressed her heartfelt thanks to Glenn Busby for his generous contribution, “We sincerely thank Glenn Busby for his selfless dedication, valuable time, and passion for the Hong Kong sporting community,” she said. “The Hong Kong Country Club is committed to giving back to the community and, through events like this, we demonstrate our belief that sports , and especially tennis, should be accessible to everyone, regardless of their background. We aim to create a unique experience for visiting players and to welcoming the general public to cheer them.”

The ITF Masters Tour, continues through 9 November, and will feature over 400 players from around the world. Admission is free, and spectators can enjoy complimentary happy hours on selected days.

Seaweed startup Uluu attracts $13.6M to scale world-first plastic alternative


PERTH, AUSTRALIA – Media OutReach Newswire – 30 October 2025 – Uluu has raised SGD$13.6 million in Series A funding to build a demonstration plant and scale its technology, transforming seaweed into a natural alternative to plastic for industrial production.

The round was led by German growth investor Burda Principal Investments with support from Main Sequence, Novel Investments (the family office of one of the world’s largest textile groups), Startmate, and a consortium of leading impact and family investors including Fairground and Trinity Ventures.

Uluu’s next-generation materials perform like conventional plastics and can be processed using existing plastic manufacturing equipment.

Unlike plastic made from fossil fuels, they are reusable, recyclable, home compostable and marine biodegradable—breaking down naturally without releasing microplastics. They’re strong, lightweight, waterproof and non-toxic, while being climate positive at scale.

At commercial scale, Uluu’s production process has scope to sequester and avoid up to ~5kg CO₂ equivalent for every 1kg of material produced, compared with ~3kg emitted by plastic today. The technology has the potential to reduce global CO₂ emissions by more than 2 gigatonnes per year.

With the Series A raise, Uluu will scale from its 100kg/year pilot facility to a 10-tonne/year demonstration plant in Western Australia, enabling the company to deliver commercial volumes to customers.

Uluu is already collaborating with a range of global partners in cosmetics, fashion and the automotive industry, including public campaigns with Quiksilver, Papinelle and Audi.

“After four years’ work developing this technology, including two years’ running our pilot plant, we’re excited to take this next step and start delivering meaningful volumes of our materials to customers,” said Uluu co-founder and co-CEO Michael Kingsbury.

“The demonstration plant is a critical step in showing Uluu can scale to truly compete with and replace fossil plastics.”

Uluu co-founder and co-CEO Dr Julia Reisser said seaweed was one of the most sustainable resources on Earth.

“Seaweed grows quickly and gets everything it needs from the sun and the sea,” she said. “It locks away CO 2 and helps clean up pollutants from the ocean.

“By harnessing seaweed, Uluu is producing materials that have a positive, rather than negative, impact on the environment, while ending plastic pollution.”

The Series A round also primes Uluu for future growth, with plans underway for a commercial-scale facility capable of producing thousands of tonnes annually to serve major global markets.

Hashtag: #Uluu #PlasticPollution #Seaweed #ESG #SeriesA #Natural



The issuer is solely responsible for the content of this announcement.

About Uluu

Founded in 2021, Uluu is headquartered in Perth, Western Australia.
– Uluu’s production process combines seaweed with fermentation—similar to brewing beer—to create natural polymers called PHAs that eliminate dependence on fossil fuels and persistent plastic pollution.
– Uluu has grown from 13 to 23 staff this year, strengthening its technical, operations and commercial teams.
– Uluu was awarded the 2025 SXSW Innovation Award in Austin, Texas.

LOTTE BIOLOGICS and SK pharmteco Sign Strategic Partnership to Strengthen Global ADC CDMO Capabilities

  • Two global CDMO leaders have joined forces to strengthen their presence in the rapidly growing antibody-drug conjugate (ADC) market.
  • The collaboration will deliver integrated, one-stop CDMO services spanning antibody drug substance, linker–payload production, and bioconjugation, supported by joint marketing based on deep ADC expertise.

SEOUL, South Korea, Oct. 30, 2025 /PRNewswire/ — LOTTE BIOLOGICS (CEO James Park) and SK pharmteco (CEO Joerg Ahlgrimm) announced that they have signed a Letter of Intent (LOI) for a strategic collaboration to strengthen their competitiveness in the global antibody-drug conjugate (ADC) market.

Leaders from SK pharmteco and LOTTE BIOLOGICS at the LOTTE BIOLOGICS booth at CPHI Frankfurt, Germany, following the signing of the strategic collaboration Letter of Intent on October 29, 2025. From left to right: Joon Chang, CBO, LOTTE BIOLOGICS; Jiwon Chun, CGO, LOTTE BIOLOGICS; Kern Chang, CTO, LOTTE BIOLOGICS; Yooyeol Shin, CSO, LOTTE BIOLOGICS; James Park, CEO, LOTTE BIOLOGICS; Joerg Ahlgrimm, CEO, SK pharmteco; Andy Fenny, CCO, SK pharmteco; Olivia Boyce, Global Head of Proposals, SK pharmteco; Shiuk Lee, CSO, SK pharmteco; Steve Barr, Head of Small Molecule, SK pharmteco.
Leaders from SK pharmteco and LOTTE BIOLOGICS at the LOTTE BIOLOGICS booth at CPHI Frankfurt, Germany, following the signing of the strategic collaboration Letter of Intent on October 29, 2025. From left to right: Joon Chang, CBO, LOTTE BIOLOGICS; Jiwon Chun, CGO, LOTTE BIOLOGICS; Kern Chang, CTO, LOTTE BIOLOGICS; Yooyeol Shin, CSO, LOTTE BIOLOGICS; James Park, CEO, LOTTE BIOLOGICS; Joerg Ahlgrimm, CEO, SK pharmteco; Andy Fenny, CCO, SK pharmteco; Olivia Boyce, Global Head of Proposals, SK pharmteco; Shiuk Lee, CSO, SK pharmteco; Steve Barr, Head of Small Molecule, SK pharmteco.

Through this collaboration, the two companies will jointly investigate providing integrated, one-stop CDMO services to global clients, offering differentiated ADC solutions that span from development to commercial manufacturing.

LOTTE BIOLOGICS will utilize its cGMP manufacturing capabilities and global quality competitiveness at its Syracuse Bio Campus in the U.S. to deliver high-quality bioconjugation and drug substance manufacturing services.

Meanwhile, SK pharmteco will be responsible for linker–payload development and manufacturing within the chemical-synthesis portion of the process, complementing LOTTE BIOLOGICS’ bioconjugation and drug-substance manufacturing.

By combining technical expertise and global networks, the companies aim to create a fully integrated CDMO platform that minimizes development-to-manufacturing gaps, offers customized solutions for clients, and strengthens competitiveness in the rapidly expanding ADC sector. 

They also plan to jointly pursue global marketing and client engagement to expand their customer base across key markets.

The partnership also aligns with the ongoing global trend toward supply chain reshoring, as each company possess advanced manufacturing infrastructures in both the U.S. and Europe. 

James Park, CEO of LOTTE BIOLOGICS, stated, “This collaboration marks a meaningful milestone, as two leading Korean biopharma join forces on the global stage. By combining our strengths in advanced modalities such as ADCs, we will reinforce Korea’s biopharmaceutical leadership and accelerate our growth in the global market.”

Joerg Ahlgrimm, CEO of SK pharmteco, added, “This strategic partnership will supercharge the development of next-generation therapeutics, positioning both companies to deliver significantly greater value and accelerate the delivery of innovative new medicines to patients around the world.”

About LOTTE BIOLOGICS

Headquartered in Seoul, South Korea, LOTTE BIOLOGICS was founded in 2022 with a mission to deliver therapies that contribute to a healthier world. At the Syracuse Bio Campus in New York, LOTTE BIOLOGICS provides high-quality GMP manufacturing services for drug substances. LOTTE BIOLOGICS is also advancing into a new area of expertise with Antibody-Drug Conjugates (ADCs) conjugation services. With over $100 million invested in ADC modalities, including both drug substance and conjugation capabilities on-site, we offer a seamless, end-to-end service from drug substance manufacturing to conjugation. Looking ahead, LOTTE BIOLOGICS is constructing three advanced bio plants in Songdo, South Korea. With construction of the first plant already underway and expected to be operational by 2027.

About SK pharmteco

SK pharmteco is a global contract development and manufacturing organization (CDMO) with production sites, research & development facilities, and analytical laboratories across the U.S., Europe, and South Korea. The company partners with biopharmaceutical companies of all sizes to manufacture Active Pharmaceutical Ingredients (API) and intermediates, cell and gene therapy technologies, registered starting materials, and analytical services for the biopharmaceutical industry worldwide. SK pharmteco is a subsidiary of SK Inc. (KRX: 034730) (SK), the strategic investment company for SK Group, South Korea’s second-largest conglomerate.

Global Times: China-South Korea Literature Salon held at Korean Cultural Center in Beijing

BEIJING, Oct. 30, 2025 /PRNewswire/ — To thoroughly study, promote, and implement Xi Jinping Thought on Culture and to advance mutual learning between Chinese and foreign civilizations, the Global Times “Reading Through the Seasons” China-South Korea Literature Salon was held on Wednesday at the Korean Cultural Center, China. The event aimed to build a new platform for cultural exchange between China and South Korea through literary dialogue.

Jointly presented by the Global Times, the Korean Cultural Center, and the World Sinology Center at Beijing Language and Culture University (BLCU), the event brought together renowned writers and translators from both countries to explore the charm of literature and listen to the symphony of East Asian literature through bilingual verses infused with the fragrance of ink. It was also a continuation of the Global Times’ “Reading Through the Seasons” series of events.

Bai Long, deputy editor-in-chief of the Global Times, said in his opening speech that he hopes this event will deepen cultural exchanges between the two countries, foster closer dialogue and more frequent mutual translations among writers, scholars, and publishers, and inspire the younger generation to explore through reading and creation the common challenges faced by humanity. 

Bai noted that the Global Times has long been a witness, recorder, and promoter of literary dialogue and cultural exchange between China and South Korea.

Kim Jin-gon, director of the Korean Cultural Center, China, told the Global Times that South Korea and China are close in geography, connected in culture, and bound by deep people-to-people ties – precious neighbors inseparably linked to each other.

Xu Baofeng, director of the World Sinology Center at BLCU, said young people represent the future of both China and South Korea, and the future of Asia. “We hope that through events like today’s literary salon, dialogue between Chinese and South Korean literature will spark new inspiration and meaningful exchanges of ideas.”

During the salon, Kim Tae-sung, a South Korean translator and winner of the 10th Special Book Awards of China; Dong Xi, president of the Guangxi Writers Association and professor at Guangxi Minzu University; South Korean writer Lee Jee; and Cui Youxue, associate professor at the School of Chinese Ethnic Minority Languages and Literature, Minzu University of China, shared their journey on the literary exchanges between China and South Korea. 

At the following roundtable discussion, Yin Hanchao, deputy director of the Chinese Studies Center of the National Library of China, said that China and South Korea both belong to the Confucian cultural sphere, therefore share common values and ways of thinking in this regard.

The speakers at the roundtable elaborated on topics such as the locality and globality of contemporary literature from both countries in the context of globalization.

In a major move of advocating for reading and literary exchanges, student representatives from China and South Korea and the hosts jointly launched a reading initiative, calling on youths from the two countries to use books as a bridge and transform literary wisdom into a driving force for action.

Since 2023, the Global Times has hosted five offline events featuring reading and literature.

Bai Long, deputy editor-in-chief of the Global Times: 

From the records of ancient Korean envoys documenting the customs and landscapes of China to the wide circulation of contemporary Chinese and South Korean literary works, books have always served as vital vessels of civilization, bonds of emotion between the two peoples, and witnesses to shared history and changing times. The vibrancy of economic and trade exchanges, coupled with the resonance between civilizations, together paints a colorful picture of the bilateral relationship and provides fertile ground for literary exchanges between China and South Korea.

Kim Jin-gon, director of the Korean Cultural Center, China:

Personally, I believe that literature is the essence of culture. When it is translated into other languages, it becomes the most accessible and profound medium for mutual understanding. I hope that today’s literary salon will serve as an opportunity to further expand exchanges and cooperation between South Korea and China in the fields of translation and publishing, deepening mutual understanding and friendship between our peoples.

Xu Baofeng, director of the World Sinology Center at BLCU:

China and South Korea share deep bonds between their peoples and a natural affinity in culture and literature, giving them unique advantages in fostering people-to-people exchanges. The World Sinology Center at BLCU will continue to work with all partners, using language as a medium and culture as a bridge, to deepen academic cooperation. Together, we hope to help Chinese and South Korean literature resonate in harmony through mutual learning, and to steer the vessel of literary friendship between our two countries across mountains and seas toward a brighter shore.

Kim Tae-sung, South Korean translator, winner of the 10th Special Book Awards of China:

South Korea is one of the countries that has absorbed the most Chinese cultural content… If you go right now to a large bookstore in Seoul, how many books related to China can you find? At least more than 1,000. Books related to Lu Xun alone exceed 100. This is probably because, as the nearest neighboring country, there is an urgent need to understand and gain knowledge about China.

Dong Xi, president of the Guangxi Writers Association, professor at Guangxi Minzu University:

Chinese and South Korean literature use the narrative shell of “transformation” to convey distinct themes. Writers from different eras and countries have all employed the motif of “transformation” to express their unique experiences and themes. Every form of “transformation” exists to achieve a sense of normalcy.

Lee Jee, South Korean writer:

Just as flowers, though sharing the same roots, blooming in different colors due to variations in soil and climate, South Korean and Chinese literature have become richer through their differences. If the globalization of literature has been advanced through translation, then the current intergenerational shift is creating another turning point. Readership has undergone more rapid and radical changes in the past decade than those witnessed over the previous hundred years.

Cui Youxue, associate professor at School of Chinese Ethnic Minority Languages and Literature, Minzu University of China:

I would like to share with you my understanding of the poetic nature of Han Kang’s literature… The poetic quality of Han’s works stems from her steadfast commitment to writing poetry and her continuous effort to infuse poetic elements into fiction.

Yin Hanchao, deputy director of the Chinese Studies Center of the National Library of China:

China and South Korea both belong to the Confucian cultural sphere, therefore share common values and ways of thinking in this regard. Chinese works To Live, Chronicle of a Blood Merchant and South Korea’s Stingray all portray fathers as responsible and devoted figures. Such universal cultural symbols resonate deeply across regions and help people empathize with one another.

Roundtable discussions

Chinese and South Korean guests communicated on reading and literary exchanges between the two countries during a roundtable session at the event.

Reading begins with our neighbors, said Dong Xi. Many of our literature courses today take a long detour before paying attention to East Asian authors. Yet when we read South Korean works, there’s a sense of familiarity: We share the same roots, our cultures are similar, and the issues we face are often alike. The most important aspect of universality lies in humanity: If a work embodies genuine human emotions, it will move readers all over the world.

Yin Hanchao said that, from a translator’s perspective, Chinese translators were already thinking about how to better translate Chinese works for the world more than a century ago. For a nation to have the vision and confidence to present its own works to the world for others to appreciate, judge, or even critique, that in itself is a true expression of cultural confidence.

In Kim Tae-sung’s view, language is the vessel of culture, and the only means to digest it is through reading. He said Chinese author Liu Zhenyun’s novels possess a kind of narrative humor, while Dong Xi’s works are remarkable for their skillful use of metaphor. Both are distinctive qualities of Chinese writers. South Korean literature should engage in deeper exchanges with Chinese literature, he said.

As a novelist, Lee Jee said we should foster closer literary exchanges through fiction. Only works written with tears and blood can evoke true empathy among people around the world – that’s how they travel beyond borders.

According to Cui Youxue, for translators, all literary history is essentially a history of translation. He believes translators have made great contributions to the development of national literatures, languages, and even to the formation of nations themselves. Reading, in turn, is a form of spiritual communication: A good novel can profoundly move the heart, and those who read feel spiritually fulfilled every day.

 

SoftwareOne Signs Strategic Collaboration Agreement with AWS to Accelerate Gen AI Innovation Across APAC


SINGAPORE – Media OutReach Newswire – 30 October 2025 – SoftwareOne, a global leader in cloud and software services, today announced a Strategic Collaboration Agreement (SCA) with Amazon Web Services (AWS) to accelerate digital transformation, cloud adoption, and generative artificial intelligence (Gen AI) innovation across the Asia-Pacific (APAC) region.

SoftwareOne Signs Strategic Collaboration Agreement with AWS
SoftwareOne Signs Strategic Collaboration Agreement with AWS

Under the multi-year agreement, SoftwareOne will enhance its AWS capabilities to support customers in Australia-New Zealand (ANZ), Southeast Asia, Greater China Region (GCR), and India. The collaboration focuses on four strategic areas: migration and modernization, data and Gen AI, launching entirely new solutions on AWS (greenfield deployments), and AWS Marketplace enablement. SoftwareOne will continue to invest in obtaining AWS certifications, ensuring SoftwareOne employees are equipped with the latest AWS expertise to support customers across the APAC region.

“This agreement marks a pivotal step in our mission to empower organizations across APAC to accelerate digital transformation using Gen AI,” said Varun Paliwal, President APAC and Middle East of SoftwareOne. “By combining SoftwareOne’s expertise with the comprehensive cloud services of AWS, we’re delivering tangible business outcomes and long-term value for our customers.”
“This collaboration with SoftwareOne demonstrates our joint focus on helping customers across APAC accelerate both cloud transformation and responsible generative AI adoption,” said Corrie Briscoe, Director of Partner Core, Asia Pacific & Japan, AWS. “By combining SoftwareOne’s deep regional expertise and trusted customer relationships with AWS’s breadth of services—including Amazon Bedrock—we’re creating practical pathways for organizations to modernize their operations, innovate with confidence, and scale solutions that drive measurable impact.”
SoftwareOne will develop and deploy a portfolio of Gen AI solutions powered by Amazon Bedrock, tailored to industries such as retail, manufacturing and financial services. To accelerate adoption, SoftwareOne will provide pre-built, AWS-validated solution templates and implementation packages, including AI assistants for specific industries and workloads, which are designed to help customers move from pilot to production faster. AWS will provide technical assistance and collaborate with SoftwareOne teams through its Generative AI Innovation Centre (GenAIIC) Partner Alliance, which SoftwareOne has joined, and which will provide access to expert-level training and delivery acceleration.
The AI Assistants that will be launched through SoftwareOne’s collaboration with AWS include:
  • Technician AI Assistant for factory troubleshooting and maintenance queries.
  • Insurance AI Assistant for personalized plan recommendations and sentiment analysis.
  • HR Policy Assistant to automate employee inquiries and HR ticket creation.
  • Product Assistant for intelligent product search, promotion discovery, and order management.
As part of the collaboration, SoftwareOne will help customers migrate to AWS through its Rapid Migration Offer, deploy a new SoftwareOne AWS Landing Zone with built-in cloud security and governance, and will list its solutions in AWS Marketplace to streamline procurement. SoftwareOne will also invest in dedicated AWS-focused sales and marketing headcount across APAC to support customers throughout their cloud journey.

This collaboration will enhance SoftwareOne’s vision of delivering flexibility, innovation, and business value for customers across industries. To explore how SoftwareOne can accelerate your cloud journey with AWS, visit: softwareone.com

Hashtag: #SoftwareOne #AWS #GenAI

The issuer is solely responsible for the content of this announcement.

SoftwareOne

SoftwareOne and Crayon have joined forces to become a global, AI-powered software and cloud solutions provider. With a presence in over 70 countries and a team of around 13,000 professionals, the combined organization brings together global scale and local expertise to help clients reduce costs, accelerate growth, and navigate complex IT environments with confidence. Leveraging deep capabilities in cloud, software, data, and AI, the company empowers organizations to modernize, innovate, and unlock the full value of their technology investments.
Exchange and Euronext Oslo Børs under the ticker symbol SWON. Visit us at

ArkBio Initiates Phase II Clinical Trial of AK0610, a Preventive Monoclonal Antibody for Respiratory Syncytial Virus Infection

SHANGHAI, Oct. 30, 2025 /PRNewswire/ — Shanghai Ark Biopharmaceutical Co., Ltd. (“ArkBio”) today announced the initiation of a Phase II clinical study of AK0610, a fully human monoclonal antibody designed to prevent respiratory syncytial virus (RSV) infection. Building on ArkBio’s previous experience and knowledge in development of RSV therapeutics, this milestone marks a major step forward in RSV prevention and enriches the company’s innovative anti-RSV drug portfolio.

The multicenter, randomized, double-blind, placebo-controlled, dose-escalation phase II study will assess the safety, tolerability, and pharmacokinetics of AK0610 Injection in healthy infants in China. The study will be conducted at five centers nationwide, jointly led by Professor Xin Ni of Beijing Children’s Hospital, Capital Medical University, and Professor Hanmin Liu of West China Second Hospital, Sichuan University.

RSV is a leading cause of acute lower respiratory tract infections (ALRTI) in children under 5 years of age worldwide. More than 80% of children become infected before their first birthday, and nearly all have been exposed at age two. Among those infected, approximately one-third may develop severe ALRTI, such as bronchiolitis or pneumonia. Infants under one year of age, particularly preterm infants, are at greatest risk of developing serious RSV-related complications, often requiring hospitalization. Given China’s large infant population and persistent RSV prevalence, the country faces a significant healthcare burden, underscoring the urgent need for novel, long-acting preventive interventions.

AK0610 is a monoclonal antibody targeting the pre-fusion F protein of RSV. It was isolated from a convalescent infant and subsequently engineered to enhance durability. Distinguished by its unique binding epitope and mechanism of action, AK0610 maintains robust neutralizing activity across RSV variants, especially RSV B strains. Preclinical data demonstrated strong antiviral activity with an excellent safety profile. In the completed phase I trial in healthy adults, AK0610 was safe, well-tolerated, and exhibited favorable pharmacokinetic properties. With an extended half-life, a single dose may provide season-long protection, positioning AK0610 as a promising new-generation long-acting antibody for prophylaxis of RSV infection in infants.

Professor Xin Ni stated:
“RSV remains the leading viral cause of hospitalization among infants and young children in China, especially those under one year of age, placing a heavy burden on families and the healthcare system. There is an urgent need for domestically developed innovative preventive antibodies capable of offering durable protection throughout the RSV season. The initiation of AK0610’s Phase II clinical study is an important milestone in advancing such preventive strategies. Evaluating its safety and pharmacokinetics in healthy infants is an essential step towards developing this antibody for China as well as the global vast infant population. We are optimistic that the study will pave the way for this promising drug candidate to safeguard the healthy growth of infants globally.”

Professor Hanmin Liu added:
“AK0610 is a fully human monoclonal antibody with a unique mechanism of action and excellent clinical potential. Its potent, highly specific neutralizing activity and extended half-life make it a strong candidate for RSV prevention. The rigorously designed phase II study will provide important data on its safety and pharmacokinetic characteristics in infants, establishing a solid foundation for future pivotal trials. Together with participating centers across the nation, we are committed to conducting this clinical trial with scientific rigor with a goal to reduce the burden of RSV-related diseases among infants.”

About ArkBio

ArkBio is a global biotech company focused on developing innovative therapeutics for respiratory, infectious, and pediatric diseases. Founded in 2014, it has built core technology platforms and a differentiated R&D pipeline through in-house R&D efforts and external collaboration. Key drug assets include ziresovir (AK0529), the first direct-acting RSV antiviral with positive pivotal phase III results, and AK0901, an ADHD therapeutic drug, both of which have filed NDA to China CDE for market approval.

ArkBio has established strategic partnerships with several multinational pharmaceutical companies and academic institutes, including Roche, Genentech, the Scripps Research Institute, the Institute of Microbiology of Chinese Academy of Sciences, domestic and international biotechnology companies, as well as venture capital institutions.

For more information, please visit: www.arkbiosciences.com 

Investor Inquiries: IR@arkbiosciences.com 

Jenscare released its multi-product portfolio’s, including LuX-Valve Plus TRINITY study, JensClip and Ken-Valve, remarkable clinical outcomes at TCT 2025 in the U.S.

BEIJING, Oct. 30, 2025 /PRNewswire/ — Jenscare Scientific Co., Ltd. (“Jenscare” or the “Company”) (HKEX: 9877), an innovative medical device company, recently released 6-month follow-up results of TRINITY Trial of LuX-Valve Plus, a promising self-developed TTVR system, and 1-year outcomes and challenging cases of JensClip and Ken-Valve, a proprietary TMVr system and TAVR (AR) system respectively, representing the Company’s diversified and high-potential multi-product portfolio, at TCT 2025 in the U.S..

6-Month Follow-up Results of LuX-Valve Plus TRINITY Study
-Released by Prof. Thomas Modine, CHU de Bordeaux-Haut-Leveque, France

TRINITY is a global prospective, multicenter, single-arm clinical trial, which primarily aims to evaluate the safety and efficacy of LuX-Valve Plus in application on patients with severe tricuspid regurgitation and high surgical risk. The study enrolled 161 patients from 20 centers around the world, among which, 18 centers were from France, Germany, Spain, Denmark, and the UK.

The average age of the patients (FAS + Roll-in group) is about 77 years old with an average STS score of 10.24%. 91.93% of the patients has atrial fibrillation, 32.92% has left heart surgery/intervention, 26.71% has pacemaker/ICD implanted. Patients are combined with multi other comorbidities, which formed a poor baseline and increased the risks of surgical treatment or difficulties of other interventional therapies. Over 75% of enrollments utilized valve sizes between 55mm and 70mm. The results show that the device success rate is about 97%, and the average device operation time is around 41.60 minutes with the shortest time being 11 minutes.

The safety indicators show that the overall CEC-adjudicated composite events rate at 6-month of FAS + Roll-in group is 19.9%. Cardiovascular mortality is 3.7%, the incidence of strokes is 0.6%, new onset renal failure is 1.2%, non-selective tricuspid valve surgery/intervention post procedure is 2.5%, major cardiac structural complications is 3.1%, severe bleeding (including fatal, life-threatening and extensive bleeding as defined by MVARC) is 5.0%, new pacemaker implantation due to AVB is only 8.7% (no change compared to that at 30 days). No events prevailed in myocardial infarction, major access site and vascular complications, and device-related pulmonary embolism.

The efficacy indicators show that the tricuspid regurgitation (TR) grade, NYHA classification, and QoL improved significantly at 6 months. 94.4% of the patients show no above moderate TR. 90.9% of them show postoperative NYHA class I/II. KCCQ score increased by around 19 pts on average. 6MWD increased by 39 meters on average.

Professor Thomas Modine concluded that LuX-Valve Plus TTVR system is an innovative device indicated for high-surgical risk patients with severe TR and demonstrates several advantages. First, it has radial-force independent anchoring mechanism, which is designed particularly for TV. Second, it indicates low demands on imaging quality, which is expected to significantly reduce device time. Third, it provides large size options, which enables wide applicability on large TV anatomies. The 6-month clinical outcomes of TRINITY Trial demonstrate good safety and performances, with improvements in quality of life and low rate of composite adverse events. The wide application on large anatomy patients provides encouraging treatment options for severe TR patients, while current therapies are limited. Further follow-ups of TRINITY trial and clinical evidence worldwide using LuX-Valve Plus system are underway. Currently, the U.S. FDA IDE-EFS for LuX-Valve Plus has completed full enrollment with excellent safety and efficacy outcomes.

Meanwhile, evidence supporting the efficacy and safety of the transjugular approach for LuX-Valve Plus was also presented. The advantages of the transjugular approach include low incidence of access site bleeding complications, reflecting high safety profile; shorter device operation time, demonstrating good procedural efficiency; and a low screening failure rate due to the anatomical structure of the jugular vein. Current data from the TRAVEL II and TRINITY studies show bleeding complication rates of 0% and 1.8% respectively, representing outstanding clinical outcomes.

One-Year Follow-Up Results of JensClip
-Released by Prof. Vinicius Esteves, University Hospitals in Cleveland, U.S.

The study of JensClip TMVr system is a prospective, multicenter, single-arm clinical trial, which primarily aims to evaluate the safety and efficacy of JensClip in application on patients with symptomatic degenerative mitral regurgitation (DMR) at high surgical risk. The study enrolled 114 patients from 18 centers in China.

The average age of the patients is about 71 years old with an average STS score of 7.65%. 63.2% of the patients has hypertension history, 41.2% has coronary artery disease, 30.7% has atrial fibrillation, and 91.2% has pre-operative NYHA class III/IV. The results show that the device success rate at 30 days is about 95%, and the average device operation time is around 67.53 minutes.

The safety indicators show that the all-cause mortality rate is 1.8%. The incidence of unplanned mitral valve intervention/surgery is 5.3%, and that of stroke is 1.8%. The incidence of renal failure, myocardium infarction, major bleeding, device releasing/locking failure, and clip related hemolysis are all 0.9%. No events prevailed in SLDA and device related air embolism.

The efficacy indicators show that the mitral regurgitation (MR) grade, NYHA classification, and QoL improved continuously at 1 year. 96.29% of the patients show no above moderate MR. 93.46% of them show postoperative NYHA class I/II. KCCQ score increased by around 20 pts on average. 6MWD increased by around 82m from the baseline.

Professor Vinicius Esteves concluded that JensClip is an innovative device intended for severe DMR, providing easy and reliable operation with unique designing features like continuous-adjustable locking system and independent grasping technique. The 1-year clinical outcomes demonstrated procedural safety and durable MR reduction.

One-Year Follow-Up Results of Ken-Valve
-Released by Prof. Anson Cheung, St. Paul’s Hospital, Canada

The study of Ken-Valve TAVR system is a prospective, multicenter, single-arm clinical trial, which primarily evaluates the safety and efficacy of Ken-Valve in application on patients with symptomatic aortic regurgitation (or combined with aortic stenosis) at high surgical risk. The study enrolled 142 patients from 15 centers in China.

The average age of the patients is about 70 years old with an average STS score of 5.87%. 61.97% of the patients has moderate to severe frailty, 71.83% has hypertension history, 42.96% has coronary artery disease, 48.59% has peripheral vascular disease, 51.41% has prior surgical history, and 99.30% has pre-operative NYHA class III/IV. The results show that the device success rate is about 97%, and the average device operation time is around 8.70 minutes.

The safety indicators show that all-cause mortality is 5.63%. The incidence of severe bleeding is 4.23%, and conversion to surgery is 1.41%. Both the incidence rate of stroke and valve migration is 2.11%. Both the incidence of acute renal dysfunction and needed for cardiopulmonary mechanical assistance is 0.7%. No events prevailed in coronary artery obstruction, thrombosis, and cardiac tamponade.

The efficacy indicators show that the aortic regurgitation (AR) reduction, NYHA classification, and QoL improved continuously at 1 year. 94.7% of the patients show no above moderate paravalvular leakage. 96.2% of them show postoperative NYHA class I/II. EQ-5D score increased by around 19 pts on average. The function and performance of Ken-Valve remain favorable with stable EOA and transvalvular gradient at 1 year.

Professor Anson Cheung concluded that Ken-Valve TAVR system is an innovative device indicated for high-surgical risk patients with severe AR or predominantly regurgitant mixed with aortic valve stenosis with several advantages. Ken-Valve has integrated clamping and radial force anchoring mechanism which can provide reliable anchoring force. It has a leak-proof ring which is expected to minimize PVL post-implantation. It provides large size options which enables wide applicability on large aortic valve anatomies. The deflectable delivery system allows better co-axiality and alignment when treating complex anatomies like horizontal heart. The 1-year clinical outcomes of the Ken-Valve Pivotal Trial demonstrated good safety and performances, with improvements in quality of life, stable EOA and transvalvular gradient, and low rate of composite adverse events. The wide application on large anatomy patients provides encouraging treatment options for severe AR patients while current therapies are limited.

About LuX-Valve Plus

LuX-Valve Plus, the proprietary TTVR system, is designed for patients with severe tricuspid TR and high surgical risk. LuX-Valve Plus breaks through multiple technical difficulties in tricuspid valve interventional therapy. With the design of innovative “interventricular septum anchoring” and “leakproof self-adaptive braided ring”, which enables non-radial anchoring of the valve implant and tend to effectively prevent AV block. LuX-Valve series product is designated by the FDA as a breakthrough device, is enrolled in the Total Product Life Cycle Advisory Program (TAP) pilot of the FDA and is selected for the Expert Panel Scientific Advice Pilot by the EMA. As of the latest update, close to 1000 implantation cases have been completed worldwide with the LuX-Valve series products, and the longest follow-up record has been over 6 years.

About JensClip

JensClip, the proprietary TMVr system, features an innovative self-locking design, which is expected to effectively improve mitral regurgitation and reduce leaflet tension. The valve clip allows for flexible shape adjustments, which is expected to enhance procedural safety and improve intraoperative maneuverability. Furthermore, its one-piece release mechanism is designed to minimize potential mis-operation risks associated with staged detachment, effectively reducing device operation time.

About Ken-Valve

Ken-Valve, the proprietary first-generation TAVR system, is designed for the treatment of patients with severe AR or combined with AS. Its innovative design accommodates a wide range of complex anatomies, significantly improving procedural safety and flexibility while reducing device operation time. It offers six annulus sizes – 23mm, 25mm, 27mm, 29mm, 31mm and 33mm. Its unique innovative design and applicability to complex anatomical challenges, such as large annulus and horizontal heart, can address the treatment needs of patients with large annulus for whom treatment options are relatively limited.

About Jenscare

Jenscare is an innovative medical device company, established in 2011. The Company has achieved a diversified and high-potential product portfolio of interventional treatment solutions for different types of structural heart diseases, including tricuspid valve disease, mitral valve disease, aortic valve disease and so on. The Company is continuing to expand its global business layout, enhancing product influence and clinical application scale, thereby laying a solid foundation for sustained high-speed growth.