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Phuc Yen Industrial Park a catalyst for investment in Phu Tho


PHU THO, VIETNAM – Media OutReach Newswire – 10 April 2026 – Approved by the Phu Tho People’s Committee, a joint venture between Vinh Phuc International Services and Industrial Zone Joint Stock Company (VISIZ) and SHINEC joint Stock Company officially broke ground on the Phuc Yen Industrial Park (Phuc Yen IP) infrastructure project on April 9.

A view of the Phuc Yen Industrial Park in Phuc Yen Ward in Phu Tho Province. — Photo courtesy of the firm
A view of the Phuc Yen Industrial Park in Phuc Yen Ward in Phu Tho Province. — Photo courtesy of the firm

Phuc Yen IP covers 111.3 hectares in Phuc Yen Ward in the northern province of Phú Thọ, with a total investment of approximately VNĐ1.98 trillion and a 50-year operating licence.

Regarded as a key project in the province’s economic development strategy, Phuc Yen IP is expected to become a magnet for high-quality investment, particularly from enterprises in technology and electronics, precision engineering, supporting industries and logistics.

Strategic location and world-class infrastructure

Phuc Yen IP enjoys outstanding connectivity, with direct access to the Noi Bai – Lao Cai Expressway, a location approximately 10 minutes from Noi Bai International Airport and strong links to major economic hubs in Hà Nội, Phú Thọ and neighbouring provinces.

All technical infrastructure is built to international standards, including internal roads, high-capacity power supply, water supply and drainage systems, a centralised wastewater treatment plant and urban landscaping – enabling businesses to begin operations immediately upon land handover.

Development timeline

  • Phase 1 (Q1/2024 – Q1/2026): Legal procedures, site clearance, construction commencement
  • Phase 2 (Q2/2026 – Q1/2027): Full infrastructure construction – site levelling, internal roads, power and water system, wastewater treatment – culminating in project completion and handover

VISIZ General Director Nguyen Hai Tung said on behalf of the investor consortium: “We are fully committed to mobilising all available resources to deliver this project on schedule, ensuring synchronised, high-quality and modern construction standards.

“Phuc Yen IP is more than a production facility – it is a sustainable industrial ecosystem where investors can build and grow their operations with confidence over the long term.”

Socio-economic impact

At full capacity, Phuc Yen IP is expected to attract dozens of domestic and international investors, generate thousands of stable employment opportunities, and contribute meaningfully to annual State budget revenues. The park will serve as a catalyst for commercial services, urban development and industrial real estate growth across Phuc Yen Ward and surrounding areas.

Media Contact:

Hotline: (+84) 333 699 996

Email: phucyen@visiz.com.vn

Website: www.visiz.com.vn

Hashtag: #VISIZ #SHINEC

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

Lynk Pharmaceuticals Announces NDA Acceptance for Zemprocitinib by NMPA

SHANGHAI, HANGZHOU, China and BOSTON, April 10, 2026 /PRNewswire/ — Lynk Pharmaceuticals Co., Ltd. (“Lynk Pharmaceuticals”), a clinical-stage innovative drug development company focused on therapies for immune and inflammatory diseases, today announced that the New Drug Application (NDA) for its core product, zemprocitinib capsules, for the treatment of moderate-to-severe atopic dermatitis (AD), has been formally accepted by the Center for Drug Evaluation (CDE) of the China National Medical Products Administration (NMPA). This acceptance marks a critical milestone in the company’s clinical development in inflammatory skin diseases and represents an important step toward Lynk Pharmaceuticals’ transition to commercialization. Zemprocitinib capsules have the potential to provide a new treatment option for patients with atopic dermatitis.

Atopic dermatitis is a chronic, relapsing, inflammatory skin disease characterized by pruritus and impaired skin barrier function, significantly impacting patients’ quality of life. Despite the availability of various treatment options, a substantial proportion of patients have inadequate responses or face long-term safety challenges, leaving significant unmet medical needs.

The NDA submission is primarily supported by positive results from a multicenter, randomized, double-blind, placebo-controlled Phase III clinical trial (NCT06277245) conducted in China. The study demonstrated that both dose groups of zemprocitinib achieved highly statistically significant improvements (p < 0.0001) compared with placebo across primary and key secondary endpoints, while also exhibiting a favorable safety and tolerability profile.

Dr. Zhao-Kui (ZK) Wan, Founder and Chief Executive Officer of Lynk Pharmaceuticals said: “The submission and acceptance of the NDA for zemprocitinib represent a significant achievement in our continued focus on autoimmune and inflammatory diseases. We remain committed to developing innovative medicines with strong clinical value and global competitiveness, and we look forward to bringing this therapy to patients with atopic dermatitis as soon as possible.”

About Zemprocitinib
Zemprocitinib is a second-generation selective JAK1 inhibitor with best-in-class potential. In addition to the completed 52-week Phase III clinical trial in atopic dermatitis, the Phase III clinical trial in rheumatoid arthritis (RA) has progressed into the treatment extension phase. A Phase III trial in ankylosing spondylitis (AS) is currently ongoing, and a Phase II trial in vitiligo is in the startup phase.

Preclinical and clinical studies have demonstrated that zemprocitinib potently and dose-dependently inhibits multiple JAK1-mediated inflammatory signaling pathways, supporting its therapeutic potential across a range of indications, including AD, RA, and AS. Compared with first-generation JAK inhibitors that have lower selectivity, zemprocitinib exhibits greater selectivity for JAK1, which may reduce the risk of off-target adverse effects. Across all completed or unblinded clinical studies, including Phase II trials in AD, RA, and AS; the Week 24 data readout from the Phase III RA study; and the completed Phase III trial in AD, zemprocitinib has demonstrated a favorable safety and tolerability profile. The incidence of serious adverse events (SAEs) and adverse events of special interest (AESIs) was comparable to placebo, and laboratory safety parameters were generally well maintained. Overall, its safety profile is consistent in all completed or unblinded studies and compares favorably with those of reported JAK inhibitors.

About Lynk Pharmaceuticals
Lynk Pharmaceuticals is a clinical-stage biotechnology company founded by senior drug R&D leaders and executives from Pfizer, Merck, and Johnson & Johnson. The company is dedicated to the discovery and development of innovative therapies for immune and inflammatory diseases. Driven by a commitment to address significant unmet medical needs, Lynk Pharmaceuticals aims to deliver differentiated therapies with global impact. To date, the company has independently or jointly advanced multiple innovative drug candidates and successfully completed numerous clinical studies.

 

Hankook Strengthens Motorsport Presence at the 2026 Hi-Tec Oils Bathurst 6 Hour

  • Hankook proves its top-tier technological leadership by serving as the official tyre supplier to the ‘Bathurst 6 Hour’ for the second consecutive year
  • Ventus TD delivered consistent grip, stability and durability across six hours of racing
  • Motorsport-derived R&D reinforces Hankook’s global premium brand positioning

SYDNEY, April 10, 2026 /PRNewswire/ — Global leading tyre company Hankook Tire & Technology (Hankook) announced that Hankook Tyre Australia successfully served as the official tyre supplier to the 2026 Bathurst 6 Hour for the second consecutive year, held from April 3 to 5 at Mount Panorama Circuit. Through this six-hour endurance competition, Hankook reinforced its commitment to high-performance motorsport and advanced tyre technology.

[Photo] 2026 Bathurst 6 Hour
[Photo] 2026 Bathurst 6 Hour

Marking the 10th edition of the Bathurst 6 Hour, the event featured 69 cars competing across multiple classes. Held on the demanding 6.2-kilometre Mount Panorama Circuit, the race stands as Australia’s premier production car endurance event, known for its combination of high-speed straights, technical corners and significant elevation changes.

The 2026 race featured intense competition, with multiple lead changes and strategic battles throughout the six-hour duration. Supercars driver Thomas Randle, alongside Ben and Michael Kavich, secured overall victory in a closely contested finish, highlighting the importance of consistency, strategy and performance in endurance racing at Mount Panorama.

As the official tyre supplier, Hankook Tyre Australia supported the event with its advanced motorsport tyre technology. Since 2025, all competing vehicles have been equipped with the high-performance semi-slick racing tyre ‘Ventus TD’, ensuring stable race performance. Engineered to perform under demanding conditions, Ventus TD delivers high levels of dry grip, consistent handling performance and enhanced durability throughout extended race sessions.

In an endurance racing environment such as Bathurst, sustained tyre performance is critical. Ventus TD demonstrated stable grip and predictable handling across extended stints, enabling teams to optimise race strategy. Its construction and compound are designed to enhance durability, heat resistance and reduced wear under varying track conditions. The tyre’s optimised contact patch and tread design enable balanced load distribution, contributing to consistent performance.

In Australia, Hankook continues to strengthen its sales competitiveness with its flagship tyre brand ‘Ventus’ while actively supporting major local motorsport events, including the First Focus Radical Cup Australia Series, the Precision National Sports Sedans Series and the Hyper Racer Hankook Australian Drivers Championship, thereby expanding its global motorsport footprint.

Hankook Tyre Australia’s participation in the Bathurst 6 Hour reflects its broader commitment to supporting motorsport platforms that demand high levels of performance, safety and technological innovation. Leveraging its global expertise in tyre development, Hankook continues to demonstrate its top-tier technological leadership. Hankook continues to supply racing tyres and sponsor teams across more than 70 major global motorsport competitions, including the ABB FIA Formula E World Championship and the FIA World Rally Championship (WRC), further solidifying the global premium positioning of its brand.

Oricell Therapeutics Closes $110 Million Pre-IPO Financing to Accelerate Global Development of Solid Tumor CAR-T Therapies

SHANGHAI, April 10, 2026 /PRNewswire/ — Oricell Therapeutics Holdings Limited (“Oricell”), a global clinical-stage biotechnology company pioneering innovative cancer immunotherapies, today announced the cumulative closing of a pre-IPO financing round in excess of $110 million. The round was co-led by Vivo Capital, Beijing Medical and Health Care Industry Investment Fund, Qiming Venture Partners, and a leading global healthcare fund. The syndicate included an international sovereign wealth fund, E-Town Capital, Luxin Venture Capital, NGS Super, Elikon Investment, and Talon Capital.

Proceeds will be strategically allocated to accelerate Oricell’s global expansion and clinical development, while strengthening its technological capabilities and paving the way to capital market milestones.

As a frontrunner in cell therapy, OriCell is focused on engineering CAR-Ts with global clinical impact, having already secured confirmatory proof-of-concept (POC) data across multiple pipelines. By leveraging its proprietary triad: the Ori®Ab antibody screening and engineering platform, the Ori®Armoring functional enhancement platform, and the OnGo (Fast) rapid CMC manufacturing expertise, the company has built a differentiated portfolio that positions it at the vanguard of the global CAR-T race.

OriCell’s lead asset, Ori-C101, is a GPC3-targeted autologous CAR-T therapy for advanced hepatocellular carcinoma (HCC). Having successfully navigated investigator-initiated trials (IIT) and a registrational Phase 1 study, the program is now gearing up for pivotal trials. Clinical readouts have demonstrated a best-in-class efficacy and safety profile, with data highlighted at major forums including the ASCO Annual Meeting. With these promising results, Ori-C101 is positioned to become the first-in-class CAR-T therapy approved globally for HCC.

Beyond its lead asset, Oricell is aggressively advancing a diverse portfolio of next-generation modalities, including secreted, rapid-production, and in vivo CAR-T programs.

Dr. Huanfeng Yang, Chairman and CEO of Oricell Therapeutics, stated: “This financing is a testament to the global potential of our science and the dedication of our team. As we approach key inflection points in our clinical programs, our priority is clear: expedite the global development of our core assets and deepening our research into revolutionary technologies, including in vivo CAR-T and solid tumor CAR-T. We are committed to delivering transformative therapies that offer real hope to cancer patients worldwide, positioning Oricell as a dominant force in the global immunotherapy arena.”

Mr. Shan Fu, Managing Partner at Vivo Capital, commented: “While cell therapy is undoubtedly the future of oncology, solid tumors remain the industry’s toughest nut to crack. Oricell distinguishes itself not just through best-in-class clinical data for its GPC3 CAR-T, but also through a pragmatic and visionary roadmap for next-generation modalities like in vivo CAR-T. We have high conviction in their integrated ‘Platform and Pipeline’ strategy and believe they are poised to set the new standard of care in the field. Vivo Capital is eager to deploy our global network to accelerate Oricell’s expansion into international markets.”

Mr. William Hu, Managing Partner at Qiming Venture Partners, stated: “As an early investor that has stood with Oricell since the Pre-A round, we have witnessed every milestone of its journey—from technological exploration to pipeline realization, and from local innovation to global expansion. We look forward to Oricell leveraging breakthrough cell therapy solutions and stronger clinical data to define the next generation of cancer care, bringing hope to patients worldwide.”

About Oricell Therapeutics

Oricell is a clinical-stage biotechnology company developing next-generation cell therapies to address unmet needs in oncology and immunology. Powered by a proprietary technology triad: Ori®Ab (antibody discovery), Ori®Armoring (T-cell enhancement), and OnGo CMC (rapid manufacturing), Oricell has advanced a diversified pipeline targeting both solid tumors and hematologic malignancies. This technical prowess and global strategy are exemplified by the development of another core candidate, OriCAR-017. Supported by compelling data from IIT in China, the program paved the way into global development, rapidly securing IND approvals from both China NMPA and US FDA, along with FDA Orphan Drug Designation (ODD) and Fast Track Designation (FTD). OriCAR-017 has demonstrated a favorable safety profile and robust efficacy in both IIT and registrational clinical trials, with data featured at leading global conferences including 2022 ASCO, 2022 EHA, 2024 ASCO, and published in top-tier academic journals The Lancet Haematology. These milestones underscore Oricell’ capabilities in regulatory strategy, clinical development, and global execution, reflecting its commitment to transforming the future of cell therapy and delivering new hope to patients worldwide. For more information, please visit: www.oricell.com.

Forward-Looking Statements

This press release contains “forward-looking statements” which are not historical facts, but instead are predictions about future events based on the beliefs as well as assumptions made by and information currently available to the management of Oricell Therapeutics Holdings Limited (“the Company” or “Oricell”). The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Such forward-looking statements involve known and unknown risks, uncertainties and other important factors that could cause the actual results, performance or achievements of the Company, or industry results, to differ materially from any future results, performance or achievement implied by such forward-looking statements. Any forward-looking statements contained in this press release speak only as of the date of this press release. The Company assumes no obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.

Sandmark Crypto Intelligence Report Shows Credible Insight Drives Investment Confidence

  • 38% of finance professionals who personally hold crypto view it as a growth opportunity with strong upside potential
  • 96% of professional investors are optimistic about crypto’s future as an asset, vs just 39% of beginner investors
  • 25% of finance professionals describe crypto primarily as a high-risk asset — falling to just 1 in 10 among those who personally invest
  • 8% of respondents cite payments utility as a reason to hold crypto, yet wider merchant acceptance and regulatory integration are seen as critical drivers of future adoption
  • 42% of finance professionals cite regulatory uncertainty as their primary barrier to greater institutional involvement

GENEVA, April 10, 2026 /PRNewswire/ — Sandmark has today published the first edition of its Crypto Intelligence Report, uncovering how credible and reliable intelligence are building real conviction among finance professionals and investors.

Michelle Fotopoulou, Chief Marketing Officer at Sandmark, commenting on the Crypto Intelligence Report
Michelle Fotopoulou, Chief Marketing Officer at Sandmark, commenting on the Crypto Intelligence Report

The study captured the attitudes and behaviours of over 5,000 finance professionals and crypto investors across Australia, Brazil, India, Singapore, South Korea, UAE, UK and the US. Conducted in partnership with the global consumer audience insights platform GWI, the report fills a significant gap in existing market research by focusing specifically on the financially literate crypto investors: those working within and alongside the financial industry.

“Most crypto research focuses on retail sentiment. We wanted to understand how finance professionals – people who work with risk and capital every day – actually perceive and engage with crypto. What we found challenges a number of assumptions,” said Michelle Fotopoulou, Chief Marketing Officer at Sandmark.

Experience contextualizes risk

Just one in ten finance professionals who own crypto perceive it as high risk, compared to 25% of the wider professional finance community. Optimism and confidence rise in line with active participation, peaking among institutional investors and long-term holders. Beginners remain the least certain. The data consistently shows that hands-on experience, supported by reliable market intelligence, is what builds genuine conviction.

Regulation is recruitment

Regulatory uncertainty remains the primary barrier to broader institutional participation, alongside volatility and governance concerns. Yet across all respondent groups, crypto is viewed as a long-term strategic asset with strong upside potential, rather than a short-term trade. As regulatory clarity improves, the market’s next growth phase is widely expected to be led by institutions.

Michelle said: “Strong regulation acts as a catalyst for engagement. As jurisdictions put protections in place, activity accelerates, with greater confidence unlocking broader adoption.”

Public figures: formative but divisive

High-profile individuals continue to play an outsized role in shaping sentiment, often in conflicting ways. Among a pre-defined shortlist of public figures, Elon Musk drives the strongest positive sentiment (51%), while Donald Trump generates the most negative (38%), despite also ranking as the second most cited positive influence (17%). Among crypto holders who identify Musk as their strongest positive influence, 77% report high optimism toward crypto’s future as an asset. The study reflects how public figures are capable of simultaneously amplifying enthusiasm and undermining trust.

An evolving but maturing market

Michelle concluded, “It’s fascinating to see the evolution of sentiment in the crypto market, particularly in the case of institutions and finance professionals. While social media drives discovery, real market data is in higher demand. Investors need consistent, actionable market intelligence to understand the evolving crypto ecosystem.”

The Sandmark Crypto Intelligence Report is available here.

About Sandmark

Established in 2025 by a Switzerland-based entrepreneur, Sandmark operates internationally with editorial hubs in Europe, the Middle East, Asia and North America. Sandmark is led worldwide by traditional and new financial media professionals who have decades of experience covering a range of markets from banking to commodities, and FX trading to equities research.

The Sandmark Team is comprised of 20+ global employees – including journalists, researchers and data analysts – that are united in the mission to deliver clear, credible, and context-rich reporting. 

Sandmark Crypto Intelligence Report: first edition of key trends shaping the digital asset landscape
Sandmark Crypto Intelligence Report: first edition of key trends shaping the digital asset landscape

 

 

FDA Accepts NDA for TLX101-Px (Pixclara®)

MELBOURNE, Australia and INDIANAPOLIS, April 10, 2026 /PRNewswire/ — Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that the United States (U.S.) Food and Drug Administration (FDA) has accepted the Company’s resubmitted New Drug Application (NDA) for TLX101-Px[1], (Pixclara®[2], Floretyrosine F 18 or 18F-FET), an investigational PET[3] agent for the imaging of glioma (brain cancer), and has assigned a PDUFA[4] goal date of September 11, 2026.

The approval of TLX101-Px will fulfil a significant unmet medical need for the characterization of recurrent or progressive glioma from treatment related changes in both adult and pediatric patients[5]. Neuroimaging of glioma with 18F-FET is already broadly recommended in international clinical practice guidelines – including NCCN Guidelines®[6] – and TLX101-Px has been granted Orphan Drug[7] and Fast Track[8] designations by the FDA.

“There remains a critical unmet need in improving our ability to image residual glioma after treatment,” said Thomas Hope, MD, Vice Chair, Department of Radiology and Biomedical Imaging, University of California, San Francisco (UCSF). “We have worked with Telix for the last three years to help leverage our clinical data to help make FET-PET[9] available to patients in the United States.”

Patrick Wen, MD, E. Antonio Chiocca, MD, PhD, Family Endowed Chair in Neuro-Oncology at Mass General Brigham Cancer Institute, added, “Distinguishing tumor progression from treatment-related change remains one of the most challenging aspects of glioma care. PET imaging with 18F-FET is an important tool in clinical practice worldwide, and the FDA’s acceptance of this application is a meaningful step toward broader access for patients and clinicians in the United States.”

Kevin Richardson, CEO, Telix Precision Medicine, added, “The FDA’s acceptance of our NDA resubmission is an important milestone for Telix. We appreciate the FDA’s constructive engagement and look forward to working closely with the Agency to urgently obtain approval and then bring this product to market for the benefit of patients.”

Telix’s FY 2026 financial guidance does not include any revenue contribution from TLX101-Px.

About TLX101-Px

TLX101-Px is a PET imaging candidate, which has been granted Fast Track and Orphan Drug designations by the FDA for the characterization of recurrent or progressive glioma from treatment related changes. TLX101-Px targets membrane transport proteins known as L-type amino acid transporters 1 and 2 (LAT1 and LAT2). This enables TLX101-Px to be potentially utilized as a patient selection and response assessment tool for Telix’s LAT1-targeting therapy candidate TLX101-Tx (iodofalan 131I), currently under investigation in the pivotal IPAX-BrIGHT trial in patients with recurrent glioblastoma[10]. TLX101-Px and TLX101-Tx have not received marketing authorizations in any jurisdiction.

About gliomas

Gliomas are diffusely infiltrative tumors that affect the surrounding brain tissue. They are the most common form of central nervous system (CNS) cancer that originates from glial cells, accounting for approximately 30% of all brain and CNS tumors and 80% of all malignant brain tumors[11]. In the U.S., there are approximately 24,000 new glioma cases diagnosed annually[12]. Glioblastoma (GBM) is a high-grade glioma and the most common and aggressive form of primary brain cancer. The mainstay of treatment for GBM comprises surgical resection, followed by combined radiotherapy and chemotherapy. Despite such treatment, recurrence occurs in almost all patients[13], with an expected survival duration of 12-15 months from diagnosis[14]. 

About Telix Pharmaceuticals Limited

Telix is a global biopharmaceutical company focused on the development and commercialization of radiopharmaceuticals with the goal of addressing significant unmet medical need in oncology and rare diseases. Telix is headquartered in Melbourne (Australia) with international operations in the United States, United Kingdom, Brazil, Canada, Europe (Belgium and Switzerland) and Japan. Telix is listed on the Australian Securities Exchange (ASX: TLX) and the Nasdaq Global Select Market (NASDAQ: TLX).

Visit www.telixpharma.com for further information about Telix, including details of the latest share price, ASX and U.S. Securities and Exchange Commission (SEC) filings, investor and analyst presentations, news releases, event details and other publications that may be of interest. You can also follow Telix on LinkedIn, X and Facebook.

Telix Investor Relations (Global)

Ms. Kyahn Williamson

SVP Investor Relations and Corporate
Communications

kyahn.williamson@telixpharma.com

Telix Investor Relations (U.S.)  

Ms. Annie Kasparian  

Director Investor Relations and
Corporate Communications  

annie.kasparian@telixpharma.com 

Telix Investor Relations (Australia)

Ms. Charlene Jaw

Associate Director Investor
Relations

charlene.jaw@telixpharma.com

Media Contact

Eliza Schleifstein

917.763.8106 (Mobile)

Eliza@schleifsteinpr.com

This announcement has been authorized for release by the Telix Pharmaceuticals Limited Disclosure Committee on behalf of the Board.

Legal Notices

Cautionary Statement Regarding Forward-Looking Statements. 
 

You should read this announcement together with our risk factors, as disclosed in our most recently filed reports with the Australian Securities Exchange (ASX), U.S. Securities and Exchange Commission (SEC), including our Annual Report on Form 20-F filed with the SEC, or on our website.

The information contained in this announcement is not intended to be an offer for subscription, invitation or recommendation with respect to securities of Telix Pharmaceuticals Limited (Telix) in any jurisdiction, including the United States. The information and opinions contained in this announcement are subject to change without notification.  To the maximum extent permitted by law, Telix disclaims any obligation or undertaking to update or revise any information or opinions contained in this announcement, including any forward-looking statements (as referred to below), whether as a result of new information, future developments, a change in expectations or assumptions, or otherwise. No representation or warranty, express or implied, is made in relation to the accuracy or completeness of the information contained or opinions expressed in the course of this announcement.

This announcement may contain forward-looking statements, including within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that relate to anticipated future events, financial performance, plans, strategies or business developments. Forward-looking statements can generally be identified by the use of words such as “may”, “expect”, “intend”, “plan”, “estimate”, “anticipate”, “believe”, “outlook”, “forecast” and “guidance”, or the negative of these words or other similar terms or expressions. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. Forward-looking statements are based on Telix’s good-faith assumptions as to the financial, market, regulatory and other risks and considerations that exist and affect Telix’s business and operations in the future and there can be no assurance that any of the assumptions will prove to be correct. In the context of Telix’s business, forward-looking statements may include, but are not limited to, statements about: the initiation, timing, progress, completion and results of Telix’s preclinical and clinical trials, and Telix’s research and development programs; Telix’s ability to advance product candidates into, enroll and successfully complete, clinical studies, including multi-national clinical trials; the timing or likelihood of regulatory filings and approvals for Telix’s product candidates, including TLX101-Px and  TLX250-Px, manufacturing activities and product marketing activities; Telix’s sales, marketing and distribution and manufacturing capabilities and strategies; the commercialization of Telix’s product candidates, if or when they have been approved; Telix’s ability to obtain an adequate supply of raw materials at reasonable costs for its products and product candidates; estimates of Telix’s expenses, future revenues and capital requirements; Telix’s financial performance; developments relating to Telix’s competitors and industry; the anticipated impact of U.S. and foreign tariffs and other macroeconomic conditions on Telix’s business, including as a result of war or other geopolitical conflicts; and the pricing and reimbursement of Telix’s product candidates, if and after they have been approved. Telix’s actual results, performance or achievements may be materially different from those which may be expressed or implied by such statements, and the differences may be adverse. Accordingly, you should not place undue reliance on these forward-looking statements.

Trademarks and Trade Names. All trademarks and trade names referenced in this press release are the property of Telix Pharmaceuticals Limited (Telix) or, where applicable, the property of their respective owners. For convenience, trademarks and trade names may appear without the ® or ™ symbols. Such omissions are not intended to indicate any waiver of rights by Telix or the respective owners. Trademark registration status may vary from country to country. Telix does not intend the use or display of any third-party trademarks or trade names to imply any affiliation with, endorsement by, or sponsorship from those third parties.

©2026 Telix Pharmaceuticals Limited. All rights reserved.

[1] Telix’s NDA was resubmitted on March 13, 2026. Telix ASX disclosure March 16, 2026.

[2] Brand name subject to final regulatory approval.

[3] Positron emission tomography.

[4] Prescription Drug User Fee Act. 

[5] Subject to FDA review and approval.

[6] Galldiks et al. Lancet Oncol. 2025 (Joint guidelines from the European Association of Nuclear Medicine (EANM), European Association of Neuro-Oncology (EANO), Society of Nuclear Medicine and Molecular Imaging (SNMMI), Response Assessment in Neuro-Oncology (RANO), The European Society for Pediatric Oncology and The Response Assessment in Pediatric Neuro-Oncology for the characterization of recurrence in glioma patients); National Comprehensive Cancer Network® (NCCN) Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Central Nervous System Cancers V1.2025.

[7] Telix ASX disclosure October 6, 2020.

[8] Telix ASX disclosure April 16, 2024. Fast Track is a process designed to facilitate the development, and expedite the review of drugs to treat serious conditions and fill an unmet medical need. The purpose is to get important new drugs to the patient earlier. More: https://www.fda.gov/patients/fast-track-breakthrough-therapy-accelerated-approval-priority-review/fast-track

[9] Positron emission tomography imaging with Floretyrosine F 18.

[10] ClinicalTrials.gov ID: NCT07100730.

[11] Goodenberger et al. Cancer Genet. 2012.

[12] CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2018-2022. Neuro-Oncology. 2025.

[13] Park et al. Journal of Clinical Oncology. 2010.

[14] Ostrom et al. Neuro Oncol. 2018.

Open Source, After Mythos

By Rob Thomas | Senior Vice President, IBM Software and Chief Commercial Officer

ARMONK, N.Y., April 10, 2026 /PRNewswire/ — There is a pattern we keep seeing in technology. When software moves from product to platform and then from platform to infrastructure, the rules change.

IBM Corporation logo.
IBM Corporation logo.

At the product stage, control can feel like an advantage. Closed systems move fast. They tightly manage the experience. They concentrate value inside a single company. That approach can work at the product stage. But once a technology becomes foundational, once other systems, institutions, and markets begin to rely on it, the bar shifts. At infrastructure scale, openness stops being ideological and starts being practical.

AI is crossing that threshold now.

Anthropic’s limited preview of Claude Mythos brings that reality into sharper focus. The company says the model can discover and exploit software vulnerabilities at a level that few human experts can match, and it has launched a gated initiative, Project Glasswing, to put those capabilities into defenders’ hands first. What matters most is not just the model itself, but what it signals: AI is no longer just a tool people experiment with. It is becoming embedded in how organizations secure systems, write code, make decisions, and create value.

At that point, the core question changes. The issue is no longer only what these models can do. It becomes how they are built, governed, inspected, and improved over time.

History is consistent on this point. As systems grow in importance and complexity, closed development becomes harder to defend. No single company can anticipate every failure mode, every adversarial use, or every operational requirement. Restricting access to powerful systems is an understandable instinct. It can look like caution. But at infrastructure scale, security improves more often through scrutiny than through concealment.

That is the enduring lesson of open source software.

Open source does not eliminate risk. It changes how risk is managed. It allows more researchers, developers, and defenders to examine systems, test assumptions, surface weaknesses, and harden code under real‑world conditions. In security, visibility is not the enemy of resilience. It is often a prerequisite for it.

This matters even more in the age of AI. If frontier models are increasingly capable of finding vulnerabilities, writing exploits, and reshaping the security landscape, we should be cautious about concentrating understanding of those systems inside a small number of companies. Critical technologies tend to be safer when more people can inspect them, challenge them, and improve them.

This is also why open systems do not destroy value. They move it. One of the oldest misconceptions about open source is that it commoditizes innovation. In practice, it usually pushes competition up the stack. As common foundations mature, value shifts toward implementation, reliability, orchestration, trust, and domain expertise. The winners are not the companies that merely own the base layer, but those that know how to apply it best.

We have seen this before with operating systems, cloud infrastructure, and developer tooling. Open foundations expanded participation, accelerated improvement, and created larger markets on top. AI is likely to follow the same path. Even in enterprise technology, leaders increasingly view open source as strategically important, especially for infrastructure modernization and emerging capabilities like AI.

There is another reason openness matters. Who gets to participate shapes what gets built. Narrow access leads to narrow perspectives. Broad access enables more researchers, startups, governments, and institutions to influence how technology evolves and where it is applied. That does not just drive innovation. It builds legitimacy and adaptability.

The Mythos moment should give us pause, but not for the most obvious reason. Yes, the capabilities are striking. Yes, the risks are real. The deeper implication is structural. Once AI becomes critical infrastructure, opacity can no longer be the organizing principle for safety.

For decades, the most reliable model for secure software has been open foundations combined with serious governance, active maintenance, and broad scrutiny. As AI enters its infrastructure phase, that same logic increasingly applies to the models themselves. The more critical the technology, the stronger the case for openness.

If AI is becoming foundational, then openness is no longer a debate. It is a design requirement.

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eFuels SEA Launches Platform to Develop eFuels Projects Across Southeast Asia Using Infinium Technology

SINGAPORE, April 10, 2026 /PRNewswire/ — eFuels SEA, Ltd. today announced its launch as a new development platform dedicated to advancing electrofuel, also referred to as eFuel, projects throughout Southeast Asia. The company will utilize Infinium’s ultra-low carbon eFuels technology to develop and deploy commercial-scale production facilities across the region, accelerating the transition to sustainable fuels.

Headquartered in Singapore, eFuels SEA will develop eFuel production facilities that convert captured carbon dioxide and renewable power into drop-in sustainable aviation fuel (eSAF) and other ultra-low carbon products. The platform is supported by an experienced Asia-based management team with expertise in energy markets, project finance, and industrial development, working in collaboration with regional partners.

Infinium, a global leader in ultra-low carbon electrofuels designed to decarbonize transportation and industrial supply chains, will license its proprietary eFuels technology to projects under development by eFuels SEA in Southeast Asia. Infinium’s technology transforms renewable electricity, water, and waste carbon dioxide into high-value liquid fuels that can be used with existing fuel supply infrastructure without modification.

“By leveraging Infinium’s demonstrated technology, we are confident of delivering economic value add, enhancing energy security and achieving climate impact in the region. We plan to work with local partners and community members to accelerate siting of these projects as a complement to local agendas for industrial development, manpower up-skilling and net-zero commitments.” said David Wang, Co-founder & CEO

“Southeast Asia has the industrial capability and policy momentum to implement decarbonization projects to truly become a leader in electrofuels. There is also an urgent need to reduce dependency on fossil fuel with sustainable energy thereby enhancing energy security.” said Tienleong Tan, Strategic Advisor, eFuels SEA. Infinium Energy is a leader in the commercialization of ultra-low carbon eFuels, operating the world’s first commercial-scale eFuels plant in Corpus Christi, Texas since 2023. A second facility based on Infinium technology is currently under construction in Pecos, Texas.

“We are pleased to collaborate with eFuels SEA to expand access to eFuels in Southeast Asia, a region uniquely positioned to scale production of sustainable aviation fuel and other low-carbon fuels” said Robert Schuetzle, CEO and Founder of Infinium.

Reducing the region’s carbon impact and its dependence on fossil fuels

Southeast Asia offers a unique combination of fuel demand fundamentals and sources of renewable energy. Countries including Singapore, Malaysia, Thailand and Indonesia are advancing hydrogen and carbon management strategies that align with large-scale eFuel deployment. These developments create favorable conditions for new projects that can support domestic decarbonization goals while positioning the region as an exporter of sustainable fuels.

Accelerating Asia’s Energy Transition

eFuels SEA plans to target development of 3-5 projects across multiple Southeast Asian countries. By combining regional project development expertise with Infinium’s advanced technology platform, the company aims to scale production to meet both domestic demand and international market opportunities.

About Infinium

Infinium is reimagining how the world powers, moves, and computes. Through Infinium Energy™, the company transforms waste carbon into ultra-low carbon eFuels that decarbonize aviation, industry, and transport. Through Infinium Edge™, Infinium advances next-generation thermal infrastructure for data centers, removing heat as a constraint to enable more efficient, high-performance computing. Grounded in chemistry and energy systems expertise, Infinium’s platforms turn carbon and heat from limits into opportunities. For more information, visit www.infiniumco.com.

About eFuels SEA, Ltd.

Based in Singapore, eFuels SEA, Ltd. is a regional platform focused on developing, financing, producing and supplying electrofuels across Southeast Asia. The company leverages renewable power, carbon capture, and Infinium’s demonstrated technology to produce sustainable fuels for aviation, shipping, and industry. With a new industrial and financial ecosystem and re-skilling of new labor force, eFuels SEA believes it can transform the region’s carbon liabilities into energy assets. For more information, visit www.efuelssea.com

CONTACT: Liz Myers, press@infiniumco.com