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Technology & Innovation

AGIBOT Marks 5,000th Humanoid Robot as Embodied AI Moves into Real-World Operations

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AGIBOT Marks 5,000th Humanoid Robot as Embodied AI Moves into Real-World Operations

SHERIDAN, WYOMING - December 8, 2025 - AGIBOT has reached a key industrialization milestone with the rollout of its 5,000th mass-produced humanoid robot at its Shanghai factory, signaling that embodied AI is moving beyond pilots and demos into scaled deployment across manufacturing, logistics and service environments.

From R&D to Scaled Production Across Three Robot Families

The milestone reflects years of work on stability, reliability and durability in embodied robotics systems. AGIBOT's portfolio now spans three mass-produced humanoid platforms, each tailored to distinct use cases and deployment environments.

Tuhk Raises US$6 Million to Build a Real-Time Anti-Fraud Collaboration Network for Global Payments

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Tuhk Raises US$6 Million to Build a Real-Time Anti-Fraud Collaboration Network for Global Payments

SHERIDAN, WYOMING - December 8, 2025 - Canadian fintech Tuhk Inc. is stepping out of stealth with a US$6 million seed round to turn fragmented fraud data into a real-time collaboration fabric between merchants, banks and service providers, as the payments industry wrestles with a cybercrime threat measured in the trillions of dollars.

Fintech Veterans Target a US$10.5 Trillion Cybercrime Problem

Founded in 2025 by veterans from Ethoca and NuData Security, Toronto-based Tuhk is positioning itself as a "real-time data collaboration platform" at the intersection of fraud prevention and payments optimization. The seed financing is led by FINTOP, with strategic participation from Lloyds Banking Group and Capital One Ventures, signalling early alignment from major issuers and card partners.

ANGA COM 2026 Puts Municipalities, In-House Networks and Interactivity at the Center of Europe's Broadband Debate

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ANGA COM 2026 Puts Municipalities, In-House Networks and Interactivity at the Center of Europe’s Broadband Debate

SHERIDAN, WYOMING - December 8, 2025 - ANGA COM 2026 is positioning itself as a central meeting point for Europe's broadband, media and connectivity ecosystem, adding new formats for municipalities, in-house networks and interactive round tables while confirming Federal Minister for Digital Transformation and Government Modernisation Dr. Karsten Wildberger as keynote speaker at the opening in Cologne on May 19, 2026.

Federal Minister Headlines Gigabit Summit at Opening

Federal Minister Dr. Karsten Wildberger will open ANGA COM 2026 with a keynote address and then join the traditional Gigabit Summit, where CEOs of leading German telecommunications companies debate the sector's most pressing challenges. His early confirmation underscores ANGA COM's role as a high-level platform where policy, regulation and industry strategy meet, bringing together the broader telecommunications sector with the digital media world.

FDA's One-Trial Plan Could Rewrite Global Drug Development Economics

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FDA’s One-Trial Plan Could Rewrite Global Drug Development Economics

SHERIDAN, WYOMING - December 8, 2025 - The U.S. Food and Drug Administration is preparing a fundamental shift in its evidentiary standards for new drugs, with Commissioner Marty Makary signaling that a single pivotal trial could soon be sufficient for approval-a move that has roiled internal leadership, unsettled some regulators and analysts, and triggered immediate recalculations in biopharma portfolio models.

From Two Pivotal Trials to One: A Structural Break

FDA Clinical Hold on Denali's Brain-Penetrant Pompe Therapy Highlights First-in-Human Safety Scrutiny

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FDA Clinical Hold on Denali’s Brain-Penetrant Pompe Therapy Highlights First-in-Human Safety Scrutiny

SHERIDAN, WYOMING - December 8, 2025 - Denali Therapeutics is facing another regulatory setback after the U.S. Food and Drug Administration (FDA) placed a clinical hold on DNL952, its enzyme replacement candidate for Pompe disease, citing preclinical hypersensitivity signals and demanding protocol changes before the company can start Phase I studies.

FDA Flags Hypersensitivity Risk Before First Human Dosing

The clinical hold, disclosed in an SEC filing, stems from "hypersensitivity reactions" observed in mouse models. While the agency has not required additional non-clinical studies, it is insisting on a more conservative first-in-human plan. Denali has been asked to lower the proposed starting dose for DNL952 and implement "revised inclusion criteria, adjusted stopping rules and unspecified safety monitoring commitments" before the program can proceed.

Praxis Scores Phase II Win in Rare Epilepsies as Ulixacaltamide Tracks Toward 2026 FDA Filing

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Praxis Scores Phase II Win in Rare Epilepsies as Ulixacaltamide Tracks Toward 2026 FDA Filing

SHERIDAN, WYOMING - December 8, 2025 - Praxis Precision Medicines has doubled down on its neurology strategy with back-to-back updates: a Phase II win for its sodium current blocker relutrigine in rare developmental and epileptic encephalopathies (DEE) and a "successful" pre-NDA meeting for its essential tremor candidate ulixacaltamide, positioning the Boston biotech as a potential new commercial player in both ultra-rare epilepsy and movement disorders.

Relutrigine Study Stopped Early for Efficacy in DEE

Praxis has halted its mid-stage EMBOLD trial of relutrigine early, after an independent data monitoring board recommended the study "stop the study early for efficacy." The Phase II EMBOLD study is evaluating relutrigine in patients with DEE linked to SCN8A and SCN2A mutations, a small but highly underserved genetic epilepsy population with limited therapeutic options and high unmet medical need.

Eisai Doubles Down on Tau as Alzheimer's R&D Broadens Beyond Amyloid

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Eisai Doubles Down on Tau as Alzheimer’s R&D Broadens Beyond Amyloid

SHERIDAN, WYOMING - December 8, 2025 - Days after Johnson & Johnson reported a mid-stage failure for its anti-tau antibody posdinemab, Eisai is using the Clinical Trials on Alzheimer's Disease (CTAD) 2025 conference to argue that tau is still a viable target-if drug designers hit the right part of the protein-while investors and scientists pivot their attention to inflammation and vascular pathways.

Anti-tau Setbacks Raise the Bar for New Entrants

Tau-directed drugs have been among the most high-profile disappointments in Alzheimer's disease (AD) R&D. J&J's recent miss with posdinemab follows last year's Phase II failure of UCB's bepranemab and Eli Lilly's inability to replicate its amyloid success with the anti-tau candidate LY3372689. Collectively, these readouts have fed a narrative that tau may be an intractable or poorly understood target for disease modification.

SprintRay's EnvisionTEC Dental Acquisition Signals a New Phase in 3D Printing Consolidation

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SprintRay’s EnvisionTEC Dental Acquisition Signals a New Phase in 3D Printing Consolidation

SHERIDAN, WYOMING - December 8, 2025 - SprintRay's acquisition of the EnvisionTEC dental product portfolio marks a strategic step in the consolidation of the dental 3D printing market, expanding its materials ecosystem, reinforcing supply resilience and giving both SprintRay and EnvisionTEC users clearer long-term pathways in digital production.

What Changes for SprintRay Customers: More Materials, Same Workflow

For existing SprintRay practices and labs, the immediate impact is about breadth rather than disruption. The EnvisionTEC dental portfolio brings additional validated resin formulations that SprintRay is adapting for its own printers, which means customers gain more material options without having to invest in new hardware.

How Chairside 3D Printing with SprintRay Rewrites the Economics of Restorative Dentistry

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How Chairside 3D Printing with SprintRay Rewrites the Economics of Restorative Dentistry

SHERIDAN, WYOMING - December 8, 2025 - Chairside 3D printing has moved from conference buzzword to everyday reality in U.S. dental practices, and SprintRay is positioning its ecosystem as a way for clinics to bring production in-house, compress treatment timelines, and turn same-day crowns into a strategic differentiator rather than a marketing slogan.

From Lab Dependency to In-Practice Production

At its core, "chairside" simply means producing the restoration in your own practice while the patient is still in your care, instead of sending cases to an external lab and waiting one to two weeks. Clinically, the workflow is familiar-examination, preparation, design and cementation remain the same-but the fabrication step moves from a third party you can't control to equipment in your operatory that you can.

HEIDELBERG's 1,000th Speedmaster CX 104 Powers Hoifu Group's Push Into China's Premium Packaging Segment

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HEIDELBERG’s 1,000th Speedmaster CX 104 Powers Hoifu Group’s Push Into China’s Premium Packaging Segment

SHERIDAN, WYOMING - December 8, 2025 - Heidelberger Druckmaschinen AG (HEIDELBERG) has reached a major milestone with the delivery of its 1,000th Speedmaster CX 104 press, a 14-unit specialty configuration bound for the fast-growing Chinese packaging printer Hoifu Group, underscoring strong demand for high-performance, value-optimized presses in the premium packaging market.

Global Bestseller Targets High-End Packaging Growth in China

The Speedmaster CX 104 has become the bestseller in HEIDELBERG's portfolio thanks to its attractive price-performance ratio and broad suitability for commercial and packaging applications. The landmark 1,000th unit will be installed at Hoifu Group's new site in Yancheng, where it will run as part of an end-to-end, Prinect-based workflow.