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Everest Medicines Announces First Patient Dosed in a Global Multi-Center Phase I Clinical Trial of Tumor-Associated Antigen Cancer Vaccine EVM14

  • The first patient had received the first dose of EVM14 injection in a global, multi-center Phase I clinical trial of Everest Medicines’ Tumor-Associated Antigen (TAA) Cancer Vaccine EVM14 at NEXT Oncology Virginia in the United States, marking an important milestone in its global clinical development.
  • The primary endpoints of the EVM14 Phase I trial are safety and tolerability, with secondary endpoints evaluating preliminary efficacy. EVM14 is Everest Medicines’ first internally developed therapeutic mRNA cancer vaccine to obtain IND approvals from both China National Medical Products Administration (NMPA) and the U.S. Food and Drug Administration (FDA).
  • EVM14, an off-the-shelf therapeutic mRNA cancer vaccine, is developed based on the Company’s proprietary mRNA platform. It is designed to treat various squamous cell carcinomas, including squamous non-small cell lung cancer (sq-NSCLC) and head and neck squamous cell carcinoma (HNSCC).
  • Patients with these cancers face limited treatment options within the current standard of care, underscoring a significant unmet medical need. As a TAA cancer vaccine, EVM14’s unique mechanism offers the potential to complement existing therapies and help delay disease recurrence, providing hope for long-term cancer-free survival.

SHANGHAI, Nov. 21, 2025 /PRNewswire/ — Everest Medicines (HKEX 1952.HK, “Everest”, or the “Company”), a biopharmaceutical company focused on the discovery, clinical development, manufacturing, and commercialization of innovative therapeutics, today announced that the first patient had received the first dose of EVM14 injection in a global, multi-center Phase I clinical trial of its Tumor-Associated Antigen (TAA) Cancer Vaccine EVM14 at NEXT Oncology Virginia in the United States, marking an important milestone in its clinical development globally. EVM14 is Everest Medicines’ first internally developed therapeutic mRNA cancer vaccine to obtain IND approvals from both China National Medical Products Administration (NMPA) and the U.S. Food and Drug Administration (FDA).

EVM14, an off-the-shelf therapeutic mRNA cancer vaccine, is developed based on the Company’s proprietary mRNA platform. It is designed to treat various squamous cell carcinomas, including squamous non-small cell lung cancer (sq-NSCLC) and head and neck squamous cell carcinoma (HNSCC). In the targeted cancer types, 96% of patients with sq-NSCLC and 97% of patients with HNSCC expressed at least one of the five target genes.1 

The EVM14 Phase I trial is a dose-escalation study with two cohorts: EVM14 monotherapy and EVM14 in combination with PD-1 monoclonal antibody. The trial enrolls patients with pathologically confirmed unresectable, advanced, recurrent, or metastatic squamous non-small cell lung cancer (sq-NSCLC) and head and neck squamous cell carcinoma (HNSCC), who have experienced disease progression after receiving at least two prior lines of standard systemic therapy for advanced or metastatic disease. The primary endpoints are the safety and tolerability of EVM14, with secondary endpoints assessing preliminary efficacy. Monotherapy dose escalation is expected to be completed in 2026, with initial safety and tolerability data anticipated. The participating clinical sites include NEXT Oncology Virginia, The University of Texas MD Anderson Cancer Center, Memorial Sloan Kettering Cancer Center in the United States, and Shanghai Chest Hospital in China.

“The first patient dosed with EVM14 in the United States marks an important milestone in translating Everest’s internally developed therapeutic mRNA cancer vaccine from technological innovation into clinical development. With IND approval also secured in China, we will accelerate clinical progress in both the U.S. and China to build a more robust global evidence base for EVM14’s clinical value,” said Rogers Yongqing Luo, Chief Executive Officer of Everest Medicines. “Patients face limited treatment options with the current standard of care, underscoring a significant unmet medical need. As a TAA cancer vaccine, EVM14’s unique mechanism has the potential to complement existing treatments and help delay disease recurrence, offering hope for long-term cancer-free survival. We look forward to seeing this innovative therapy demonstrate promising potential in upcoming clinical trials, driving breakthroughs in cancer treatment and bringing new hope to patients worldwide.”

In preclinical studies, EVM14 induced a dose-dependent antigen-specific immune response in mice and significantly inhibited tumor growth in multiple syngeneic tumor models. Notably, EVM14 demonstrated the ability to induce immune memory and prevent tumor recurrence, offering hope for long-term cancer-free survival. Furthermore, preclinical data demonstrated that the combination of EVM14 with immune checkpoint inhibitors (ICIs), such as anti-PD-1 or anti-CTLA-4 antibodies, greatly enhanced the anti-tumor activity, reduced recurrence, and supports clinical exploration of combination therapies.

Everest Medicines continues to focus on achieving key breakthroughs in its core proprietary pipeline while accelerating the clinical development and global expansion of innovative assets with global rights. Leveraging its industry-leading mRNA therapeutic cancer vaccine platform, the Company is building a globally competitive R&D pipeline.

EVM 14 injection used in this trial was manufactured at Jiashan manufacturing site with the Company’s proprietary mRNA platform and in full compliance with global GMP standards. This demonstrates the Company’s end-to-end capabilities across the entire mRNA value chain, from proprietary antigen design, LNP delivery system, CMC process development to in-house manufacturing, laying a solid foundation for future pipeline advancement and commercialization.

Reference:

  1. The Cancer Genome Atlas (TCGA) data

About EVM14

EVM14 Injection is a preservative-free, sterile mRNA-lipid nanoparticle (mRNA-LNP) cancer vaccine. It is formulated with mRNA solution encoding 5 tumor-associated antigens (TAAs), encapsulated in a lipid nanoparticle system. After intramuscular injection, EVM14 is taken up by antigen-presenting cells (APCs) and translated into target antigens. These antigens are processed, presented to T cells by major histocompatibility complex (MHC) molecules and activated antigen-specific T cells. The activated T cells can migrate to tumor tissues, recognize, and kill the tumor cells expressing the target antigens.

About Everest Medicines

Everest Medicines is a biopharmaceutical company focused on discovering, developing, manufacturing and commercializing transformative pharmaceutical products and vaccines that address critical unmet medical needs for patients in global markets. The management team of Everest Medicines has deep expertise and an extensive track record from both leading global pharmaceutical companies and local Chinese pharmaceutical companies in high-quality discovery, clinical development, regulatory affairs, CMC, business development and operations. Everest Medicines has built a portfolio of potentially global first-in-class or best-in-class molecules in the company’s core therapeutic areas of renal diseases, infectious diseases, autoimmune disorders and ophthalmic diseases. For more information, please visit its website at www.everestmedicines.com

Forward-Looking Statements

This news release may make statements that constitute forward-looking statements, including descriptions regarding the intent, belief or current expectations of the Company or its officers with respect to the business operations and financial condition of the Company, which can be identified by terminology such as “will,” “expects,” “anticipates,” “future,” “intends,” “plans,” “believes,” “estimates,” “confident” and similar statements. Such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, or other factors, some of which are beyond the control of the Company and are unforeseeable. Therefore, the actual results may differ from those in the forward-looking statements as a result of various factors and assumptions, such as future changes and developments in our business, competitive environment, political, economic, legal and social conditions. The Company or any of its affiliates, directors, officers, advisors or representatives has no obligation and does not undertake to revise forward-looking statements to reflect new information, future events or circumstances after the date of this news release, except as required by law.

National Cancer Institute Broadens Partnership with Medidata to Bring Unmatched Continuity of Medical and Clinical Data for Lead Protocol Organizations

The Medidata Data Experience offering will enable the National Cancer Institute Lead Protocol Organizations to expedite the development of life-saving medicines for patients

SINGAPORE, Nov. 21, 2025 /PRNewswire/ — Medidata, a Dassault Systèmes brand and leading provider of clinical trial solutions to the life sciences industry, today announced that Medidata Health Record Connect and Medidata Rave Companion, both integral components of the Medidata Data Experience, will be available to a select set of National Cancer Institute (NCI) Lead Protocol Organizations (LPO). These solutions automatically enable patient data from electronic health records (EHR) systems to be elevated into the Medidata Platform, reducing administrative burdens, providing medical and clinical new levels of insights, and giving sites more time to focus on patient care.

“For years, the industry has struggled with a scalable way to use EHR in clinical studies. With Health Record Connect and Companion, we’re finally solving that challenge for NCI LPOs,” said Wayne Walker, senior vice president, Data Experience, Medidata. “By reducing duplicative tasks for research sites, we’re not only making it easier for patients to participate in trials but also accelerating timelines and improving overall data quality. This technology is a game-changer for bringing therapies to market more reliably and enhancing the experience for both researchers and patients.”

Health Record Connect and Rave Companion simplify access to a clinical trial site’s EHR data and enable automated and accurate completion of clinical trial site data entry tasks. These solutions are seamlessly integrated with the entire Data Experience, supporting both site and patient data collection and empowering NCI LPOs with the potential to input data up to 90% faster.

Medidata has supported the NCI Cancer Therapy Evaluation Program (CTEP) study portfolio with tools across the Medidata Platform for the past 17 years, strengthening the collaboration and reinforcing NCI’s ability to manage clinical operations effectively.

To learn more about the Medidata Data Experience and its solutions, visit here.

About Medidata
Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 36,000 trials and 11 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com. Listen to our latest podcast, from Dreamers to Disruptors, and follow us at @Medidata.

About Dassault Systèmes
Dassault Systèmes is a catalyst for human progress. Since 1981, the company has pioneered virtual worlds to improve real life for consumers, patients and citizens. With Dassault Systèmes’ 3DEXPERIENCE platform, 370,000 customers of all sizes, in all industries, can collaborate, imagine and create sustainable innovations that drive meaningful impact. For more information, visit: www.3ds.com.

About the National Cancer Institute (NCI)
NCI leads the National Cancer Program and NIH’s efforts to dramatically reduce the prevalence of cancer and improve the lives of people with cancer. NCI supports a wide range of cancer research and training extramurally through grants and contracts. The Cancer Therapy Evaluation Program (CTEP) manages a broad range of clinical trials that are closely integrated with preclinical discovery and development and biostatistical expertise fostered by other Division of Cancer Treatment and Diagnosis (DCTD) programs. Once a treatment approach has demonstrated promising efficacy and adequate safety in preclinical testing, CTEP-supported clinical trials networks and resources can move the therapy from first-in-human safety trials through definitive, randomized, controlled trials. CTEP also provides centralized infrastructure and support for other NCI-supported clinical trials networks, improving efficiency and reducing costs. For more information about cancer, please visit the NCI website at cancer.gov or call NCI’s contact center at 1-800-4-CANCER (1-800-422-6237).

Lazada Dominates Southeast Asia Authenticity-Driven ECommerce, Celebrates 170,000-Strong Brand Ecosystem at LazMall Brand Gala Dinner

SINGAPORE, Nov. 21, 2025 /PRNewswire/ — Lazada, Southeast Asia’s leading eCommerce platform, celebrated its 170,000-strong brand ecosystem at the LazMall Brand Gala 2025, cementing its position as the platform-of-choice for businesses in the region. A night of recognition, inspiration, and innovation, the event at Grand Hyatt Hotel Singapore brought together top brands, industry leaders, and key partners to celebrate the achievements shaping the region’s eCommerce landscape.

LazMall Brand Gala 2025 honours outstanding brand partners across Southeast Asia.
LazMall Brand Gala 2025 honours outstanding brand partners across Southeast Asia.

A Night to Celebrate Brand Excellence

The gala highlighted Lazada’s brand-led strategy and the commercial success brands achieve on Lazada:

  • Million-dollar GMV brands surged 53% since 9.9, proving the platform drives tangible results.
  • During 11.11, LazMall brands achieved a 39% GMV increase, with 11% YoY growth in LazMall buyers, demonstrating a clear shift toward trusted, high-quality brands.
  • Average revenue per user (ARPU) grew 70%, with buyer penetration at 65%, demonstrating Lazada’s ability to attract and retain premium shoppers.

“Lazada is the engine powering Southeast Asia’s eCommerce growth,” said Iris Wei, Group President of Lazada. “Our partners succeed because Lazada delivers unparalleled reach, innovation, and results for international and local brands. From record-breaking mega sales to everyday shopper trust, our joint success is built on the dedication, innovation, and collaboration with our brand partners.”

Lazada Leading the Way in Innovation and Shopper Experience

Beyond celebrating achievements, the gala underscored Lazada’s vision for the future. Lazada’s next-generation capabilities to empower brands include:

  • AI-powered tools for smarter product listings, marketing, and operational efficiency.
  • Upgraded logistics and customer service to ensure faster delivery and seamless after-sales experiences.

With these innovations, Lazada continues to empower brands to scale with ease, delight consumers, and set new benchmarks for Southeast Asia’s eCommerce landscape.

About Lazada Group

Lazada Group is Southeast Asia’s pioneer eCommerce platform. For the last 13 years, Lazada has been accelerating progress in Indonesia, Malaysia, the Philippines, Singapore, Thailand and Vietnam through commerce and technology. Today, a thriving local ecosystem links about 160 million active users to more than one million actively-selling sellers every month, who are transacting safely and securely via trusted payments channels and Lazada Wallet, receiving parcels through a homegrown logistics network that has become the largest in the region. 

Global South Talks: China Southern Power Grid Steps Up China-Africa Energy Cooperation

JOHANNESBURG, Nov. 21, 2025 /PRNewswire/ — According to a report by Xinhuanet:

On November 13, the Global South Media and Think Tank Forum China-Africa Partnership Conference got underway in Johannesburg, South Africa. A representative from China Southern Power Grid Co., Ltd. (CSG) was invited to address the “Global South Talks” session during the opening ceremony, sharing the company’s on-the-ground experience in power-grid cooperation with countries across the Global South.

Sun Shengjun, Project General Manager of the Africa and Europe Regional Development Department at China Southern Power Grid International, described CSG’s experience and efforts to deepen China–Africa energy ties in Cairo, Egypt. In 2023, Sun and his team arrived in Cairo to address chronic problems in the local power grid, including high line losses and poor operating performance. They progressively introduced CSG’s operational measures for cutting distribution network losses and rolled out practical, scalable and replicable “CSG Solutions” for the local utility. In addition to its technical efforts, CSG has focused on developing a skilled local workforce through targeted training programs and technical knowledge-sharing sessions. By matching its technology to on-the-ground operating realities and investing in workforce training, the company has sought to align its mature technical systems with local needs while fostering homegrown technical capabilities, laying the groundwork for long-term engagement.

Sun said that CSG does not regard energy cooperation as a one-way street, but as a partnership rooted in mutual benefit and shared growth. Looking ahead, the company says it will continue to provide its technologies and management expertise to Global South countries, aimed at deepening China–Africa energy cooperation and supporting plans for broader collaboration across the Global South.

Accident in Texas Leaves Two Lao-American Monks in Critical Condition

Buddhist monks in Texas begin walk for peace. (Photo: Huston Cornicles)

Two Buddhist monks participating in the nationwide Walk of Peace initiative to Washington, D.C., were critically injured on 19 November after a truck struck a pilot vehicle accompanying the group along US-90 in Dayton, Texas. 

Among those hurt is Maha Dam Phommasan, Abbot of Wat Buddha Khanti in Atlanta, who remains in critical condition. One monk was airlifted to a Houston-area hospital and is undergoing surgery, while the other sustained minor injuries and was transported by ambulance.

The Laotian American Society confirmed the incident, noting Abbot Maha Dam Phommasan’s longstanding role as a respected spiritual leader and dedicated supporter of community programs. 

Organizers reported that “the monks remain resilient” and plan to continue their journey once the injured monk’s condition stabilizes.

Emergency responders acted quickly to provide treatment, and the driver of the truck involved is cooperating with authorities. 

The Society expressed its sympathy to all those affected and pledged ongoing support for the monks, their families, and their communities. Supporters around the world have also sent prayers and messages of encouragement.

Taiwan Medical Textile Alliance Expands into Thailand’s Healthcare Market with Innovative Functional Fabrics


TAIPEI, TAIWAN – Media OutReach Newswire – 21 November 2025 – Amid global market shifts and intensifying competition, Taiwan’s leading functional and smart textiles expert, Asiatic Fiber Corporation, has united medical device manufacturers and textile suppliers to form the Taiwan Medical Textile Alliance. The alliance leverages Taiwan’s strengths in medical innovation and advanced textile production to promote cutting-edge, functional healthcare products across Southeast Asia.

Taiwan Medical Textile Alliance Expands into Thailand’s Healthcare Market with Innovative Functional Fabrics

Focusing on Thailand’s fast-growing medical tourism sector and rising demand for medical textiles, the alliance developed the “Air Scrub Suit” and graphene-based “Pain Relief Sleeves”, designed for the region’s tropical climate. These products combine comfort, functionality, and sustainability to meet the evolving needs of Thailand’s healthcare providers.

To navigate a competitive procurement environment, the alliance employs digital and AI-powered precision marketing tools, along with LinkedIn outreach, to connect with professional medical buyers. The alliance also participated in Medical Fair Thailand 2025, where it organized a large-scale product debut showcase, targeting over 100 Thai companies and institutions, including medical garment manufacturers, hospitals, and rehabilitation chains. With support from the Taiwanese government, the alliance successfully boosted brand recognition and sales in Thailand’s healthcare market, laying a strong foundation for future expansion into other regional markets and reinforcing Taiwan’s position as a global leader in advanced medical textiles.
Hashtag: #TaiwanInnovativeSoftwareandServicesAssociation

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

Vietnam Flooding Submerges Homes, Kills 41, After Relentless Rain

Vietnam Flooding Submerges Homes, Kills 41, After Relentless Rain
People (L) wade through floodwaters near inundated vehicles in Nha Trang, Vietnam's coastal province of Khanh Hoa on November 20, 2025. (photo credit: DUC THAO / AFP)

AFP – Rescuers plucked stranded people from the rooftops of submerged homes as widespread flooding inundated central Vietnam, where authorities said on 20 November at least 41 people were killed.

xTool Launches “Make It Here” Initiative to Fuel a European Renaissance of Making


BERLIN, GERMANY – Media OutReach Newswire – 21 November 2025 – xTool, a global leader in desktop laser cutters and smart fabrication tools, today launched its “Make It Here” initiative, underscoring its expanded commitment to Europe through localisation efforts, community programs, and new tools designed for creators, local workshops, and education.

xTool Launches “Make It Here” Initiative to Fuel a European Renaissance of Making
xTool Launches “Make It Here” Initiative to Fuel a European Renaissance of Making

Revealed at the company’s European brand launch event in Berlin, xTool presented a roadmap to empower creators, small businesses, and local studios — the ecosystem driving Europe’s modern making renaissance. With new partnerships, tools, and community initiatives, xTool aims to bring manufacturing power closer to where ideas begin.

Driving Local Manufacturing Forward

As part of its long-term European strategy, xTool announced new investments that strengthen its operational footprint and support the region’s shift toward flexible, localised production.
With a soon-to-open German office, more than 200 demo rooms, and a growing partner network, xTool enables SMBs, designers, educators, and independent makers to build high-quality micro-manufacturing systems that are accessible, professional, and locally rooted.

“Europe has one of the strongest traditions of craftsmanship and creativity,” said Jessie Liu, President of xTool. “Our mission is to support that spirit with accessible, industrial-grade tools and long-term local investment.”

Building Success From the Ground Up

The event highlighted real success stories, including German entrepreneur Kerstin Bauer, who used xTool technology to turn custom apparel from a service into a scalable micro-production model.

To expand access to such opportunities, xTool introduced its 1% Donation Initiative, committing 1% of annual profit to local maker communities, youth programs, Fab Labs, and skill-building organizations.
In 2025, beneficiaries include TU Berlin, Fraunhofer, Z-Lab, MotionLab Berlin, and smz-karlsruhe — institutions supporting hands-on innovation and maker education across Europe.

Innovation for Every Workshop

xTool also unveiled the F2 Ultra UV, a precision laser designed for premium personalization and delicate materials. Using UV “cold” processing, it delivers clean, micron-level engraving on glass, crystal, ceramics, and engineered plastics. The F2 Ultra UV will be available in Europe from 27 November 2025, starting at 3,919 EUR.

Panel Highlights

In a panel featuring Jessie Liu, Kerstin Bauer, and Jean-Michel Molenaar from the Fab Foundation — moderated by tech communicator Sascha Zöller — speakers explored how technology, community, and micro-production can accelerate Europe’s creator-led manufacturing movement.

Hashtag: #xTool

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

About xTool

xTool is a global leader in desktop laser cutters, engravers, and smart fabrication tools. Since 2020, xTool has empowered creators in over 62 countries, supported by 515 patents and 48 world-first innovations. xTool is transforming how people learn, create, and build—from classrooms to research labs, from garages to retail stores. Combining powerful technology with intuitive design, xTool makes advanced fabrication tools accessible to makers, educators, and entrepreneurs everywhere. Learn more at.