Coverfoto van chiron
chiron

chiron

Biotechnologie

Human-relevant in vitro models and preclinical services designed to support confident drug development decisions

Over ons

chiron is a pre-clinical CRO and platform company specializing in advanced, human-relevant in vitro models for translational drug discovery and development. We partner with pharma and biotech organizations to generate predictive efficacy, safety, and mechanistic data that supports confident decision-making early in development — before costly in vivo and clinical studies. Our proprietary platforms integrate 3D biology, mechanobiology, and flexible study design to address disease areas where conventional in vitro models fail to capture key biological drivers. What makes chiron different • Human relevance first: disease-relevant architecture, human cells, and physiological cues • Mechanism matters: beyond phenotypes, we deliver mechanistic insight • Decision-grade data: designed to inform real go/no-go decisions • Flexible partnership: bespoke studies aligned with program needs Core disease areas • Oncology & Immuno-Oncology • Arthritis & Joint Disease Our platforms µMass™ — A scalable 3D micro-aggregate platform enabling reproducible, long-term efficacy, toxicity, and MOA studies compatible with standard laboratory workflows. Re-Plate™ — A mechanobiology-enabled in vitro platform that incorporates controlled mechanical stimulation to reveal force-dependent disease mechanisms and drug responses. Who we work with • Pharma & biotech teams seeking translational confidence • Researchers adopting advanced in vitro systems for biologically relevant studies chiron delivers in vitro data designed not just to inform — but to decide.

Website
http://www.chrn.co
Branche
Biotechnologie
Bedrijfsgrootte
2-10 medewerkers
Hoofdkantoor
Maastricht
Type
Particuliere onderneming
Opgericht
2022
Specialismen
Organ on Chip, Cartilage, Arthritis, in vitro models, tissue regeneration, organoid, aggregates en drugs

Locaties

Medewerkers van chiron

Updates

  • At chiron we know the importance of standardization. That is why we are actively participating in the standardization of organ-on-chips and organoids!

    Organisatiepagina weergeven voor IAMPS.

    771 volgers

    We are delighted to announce that IAMPS has been admitted as a Category A liaison to ISO Technical Committee 276/SC 2, which is leading the development of international standards for Microphysiological Systems (MPS) and Organ-on-Chip (OoC) technologies. As the broadest liaison status, Category A enables IAMPS to actively contribute across the Committee's work, including: 🔹 Terminology, stakeholder environment and interdependencies in MPS and OoC 🔹 Biological components in MPS and OoC 🔹 Engineering, manufacturing and design of MPS and OoC 🔹 Experimental design, data processing and integration of MPS and OoC studies 🔹 Characterisation of materials and processes Standardisation is essential to the future of the MPS industry. Well-designed standards improve quality, reproducibility, and trust, helping to accelerate adoption and facilitate collaboration and trade. At the same time, standards must remain flexible enough to support innovation in a rapidly evolving field. IAMPS is committed to working with ISO TC 276/SC 2 to help develop standards that strike the right balance: fostering confidence while enabling innovation. The association liaison will reinforce the presence of its members Carlo Alberto Paggi, PhD Pagani from chiron, Paola Occhetta from BiomimX® Srl and Bas Trietsch from MIMETAS. We would like to sincerely thank the members of ISO TC 276/SC 2 for their positive vote in support of IAMPS' Category A liaison. We look forward to contributing our expertise with the Committee to advance the MPS ecosystem. #IAMPS #OrganOnChip #MicrophysiologicalSystems #Standardization #ISO AlveoliX, BiomimX® Srl, Dynamic42 GmbH, chiron, InSphero, MIMETAS, NETRI, React4life, TissUse GmbH. https://lnkd.in/gZJ_Ut6d

  • We are pleased to share a new update from the OPZuid-supported INTELLECTUALS project, where our consortium is developing a high-throughput 3D cartilage-on-a-chip platform for osteoarthritis research. During the latest reporting period, the project made strong progress across manufacturing, quality control, biological validation, and hydrogel integration. A major milestone was the manufacturing and testing of cells and hydrogel injection. The consortium also continued to advance: • scalable manufacturing and alternative material processing • quality-management documentation and SOP development • sterilization, packaging, and labelling activities • validation with patient-derived chondrocytes • hydrogel formulation and integration into the chip platform The project’s results have also been presented at international conferences, helping to raise awareness of the potential of organ-on-chip technologies to improve osteoarthritis research and drug development. This progress is the result of close collaboration between chiron, University of Twente, Maastricht University, TNO, Medace BV, and Hy2Care® BV. We look forward to the next phase: expanding production qualification, continuing biological validation, and further demonstrating the platform’s potential for more predictive and human-relevant osteoarthritis research. We would like to thank STIMULUS and all the other funding bodies that are currently supporting this project! #OPZuid #INTELLECTUALS #OrganOnChip #CartilageOnChip #Osteoarthritis #Biotechnology #MedTech #DrugDevelopment #Innovation #Collaboration

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  • Another important milestone for chiron! Sensors and organ-on-chip (or advanced in-vitro models) will be the gold standard of pre-clinical research! By joining forces with scientists/researchers across Europe we plan to create disruptive technologies that can bring new therapies to market in a shorter and more reliable way!

  • chiron heeft dit gerepost

    Some of the companies at BIO this week won’t survive the next five years. After four days on the floor, it wasn’t difficult to see which ones are positioning themselves to thrive and which ones are not. This was the best BIO International Convention I’ve attended in close to a decade. Roughly 22,000 people. A packed exhibit hall every afternoon. The industry is back. The energy was real, and people were there to build partnerships and make deals. But one of the most significant technologies changing the industry was AI. Not on the edges. Front and center, with an entire section of the exhibit hall dedicated to AI companies. And the progress is real, across discovery, data generation, interpretation, prediction, imaging, and operational intelligence. Nearly every part of drug development is being reshaped. Here’s what was obvious on the floor. The organizations that embrace these technologies will become more productive, scale faster, and operate with greater precision and lower risk. Those that hesitate will find it increasingly difficult to compete. The second major shift was equally significant: NAMs. Advanced 3D in vitro systems are changing how we generate evidence before and alongside clinical trials. Higher quality human-relevant data leads to more informed development decisions. Combine AI with these technologies, and the opportunity is substantial: faster learning cycles, more informed decisions, and ultimately medicines that are more effective and less toxic. That future felt tangible at BIO this week. It was also great catching up with Dustin Dopsa and Carlo Alberto Paggi, PhD from chiron. The science throughout the conference was extraordinary. The companies that win won’t simply have the best science. They’ll be built to move at the speed modern science now demands. The next competitive advantage in biotech won’t be the science alone. It will be an organization’s ability to translate science into business decisions faster than everyone else.

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  • We're in San Diego for work. WE SWEAR! Don't believe us? Drop by the Health Holland booth at the BIO International Convention to say hello! We've got lots to talk about: human-relevant data for de-risking clinical trials, a portfolio of applications in #oncology, #arthritis, and always building more, Jason Derulo, the gorgeous weather in San Diego, last night's San Diego Padres win against the Braves... whatever your fancy, we've got you covered! #BIO #NL #NAMs #seeThingsDifferently

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  • This year has already been full of adventures and activities! From the beautiful beaches in Goa (India) to the incredible lights of Shanghai (China), chiron is exploring possibilities world wide! But is not only about chiron! This post is specific for the people attending the ARI Orthopaedics Conferences in Davos! Here, our collaborators will be presenting data obtained using chiron’s technologies!   From the presentation of Tim Welting (Exploring the bioactivity of synovial fluid in osteoarthritis as a vector for intra-joint biomolecular cross-talk) to the posters of Laura Mecchi (A Cartilage-on-Chip Platform for Human MSC Mechanobiology) and Zahra Sarmadian (Synergistic Effects of Mechanical Loading and Inflammation on Chondrocyte Gene Expression in a Cartilage-on-Chip Model) there is going to be a lot of interesting scientific discoveries! We would like to wish all the participants a wonderful event and if you are interested in the platforms here is the link: https://www.chrn.co/ #mechanical #stimulation #science #future #technology #standard #NAMs #Robust #Reproducible #Human #Relevant

  • chiron heeft dit gerepost

    Organisatiepagina weergeven voor IAMPS.

    771 volgers

    The EU must significantly increase and better target funding for NAMs to deliver on its policy ambitions and maintain its position in the increasingly competitive global microphysiological systems MPS landscape. This was the key message delivered by IAMPS representatives at a recent European Parliament event entitled “Funding for non-animal science: Moonshot for NAMs”. IAMPS is supporting the proposal of a Moonshot for NAMs championed by the BioMed21 Collaboration which would lead to a €1 billion funding programme for the sector in the next Horizon 2028-2034 Programme. ‘Moonshots’ are major projects proposed by the European Commission to position Europe as a global leader in strategic fields: such an initiative is urgently needed for the MPS sector. Future funding must place greater emphasis on higher technology readiness level (TRL) projects that can qualify and deploy existing MPS models for end-users. This is vital for the future of the industry, but also to fulfil major EU policy goals. The EU Biotech Act, in its current draft, designate NAMs as strategic technologies for Europe; the EU Life Science Strategy 2025-2030 also lists the sector as a key to accelerate innovation and de-risk the development of new medicinal products; and the EU Roadmap towards phasing out animal testing for chemical safety assessments makes ambitious goals for replacement animal tests. NAMs are increasingly central to the EU’s ambitions, and Europe’s MPS industry is well positioned to deliver. However, success will require sustained, strategic investment. Without it, both the sector and the EU’s broader policy goals are at risk. We warmly thank the organizers, MEP Cristina Guarda and MEP Sebastian Everding, as well Francesca Pistollato, Antigoni Effraimidou, Jo Swabe and Fabia Furtmann from Humane World for Animals and the all the participants for the lively discussions during and after the event. In the picture: Jos Joore from MIMETAS, Vice-President for Programmes and Legislation at IAMPS; Carlo Alberto Paggi, PhD from IAMPS founding member chiron and Helder Constantino, IAMPS Managing Director. AlveoliX, BiomimX® Srl, Dynamic42 GmbH, chiron, InSphero, MIMETAS, NETRI, React4life, TissUse GmbH. #NAMs #MicrophysiologicalSystems #MPS #HorizonEurope

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  • WARNING: this post was NOT generated with AI. It may evoke real thoughts and emotions! Before Carlo Alberto Paggi, PhD and Dustin Dopsa embarked on the journey we call, chiron, both of them worked at big-name corporate companies. The things they learned during those phases of their career were, and are, absolutely essential for how we go about tackling challenges, creating solutions, and developing products at chiron, only a daily basis. It’s ALL about the end user.  Regardless if it’s a service we provide, or a piece of technology that lands in the hands of the user, the real question is: “are we doing something that actually benefits our customers?”. We approached μMass™ in the same manner. We built a foundational platform, upon which we have now developed various human-biology applications, to answer the questions of pharma drug-development teams. In every step of the way, we ensured that the product and corresponding portfolio of services we were creating, would have a strategic impact on those same drug-development teams. If this speaks to you, and you haven’t been in touch with us yet, please reach out. We’d be very happy to meet you, and hear more about what you’re working on. #microMass #humanRelevantData  #3DCellCulture #customerIsKing

  • A tumour isn't a clump of cells, it's a fortress! WITH WALLS! And guess what? Most lab models pretend the walls aren't there. The clip below is an extended cut from the µMass™ video we launched back in April. In it, our Co-founder Carlo Alberto Paggi, PhD points to a problem cell-therapy developers know well: a solid tumour is wrapped in a dense barrier of cells a therapy has to break through before it can work; a flat 2D culture simply can't show you that. So, the data you'd base a decision on doesn't reflect the disease. Solving real-world problems like the one mentioned above, for the pharmaceutical industry, is why chiron exists. We're not coming up with clever technologies in search of an industry to adopt it—it's exactly the reverse. The problems we build for are ones our own founders and scientists ran into inside pharma and biotech. We know the questions drug developers actually need answered, and the standard of evidence it takes to answer them. µMass™ is one of the ways we answer those questions: a platform, with applications built on top of it, enabling human-relevant, 3D aggregate data, reproducible and traceable enough to support real development decisions in solid-tumour oncology, arthritis, liver, and beyond. chiron is industry, for the industry; and for those, who see things differently. #pharma #cellTherapy #oncology #spheroids #microMass

    How can we leverage the power of advanced in vitro models such as organ-on-chip to gain insights on the mechanisms of action of specific therapies? How can we make sure to have robust and reproducible data that can be used to better optimize clinical outcomes? At chiron have created μMass™. μMass™ delivers human-relevant data enabling drug-efficacy findings in solid-tumour oncology, liver, cardiac, as well as many other 3D cell-aggregate applications. We have already supported scientists and researchers across the world in the optimization and assessment of their therapies! What are you waiting for? Join us in providing a better solution to patients ! #future #innovation #human-like

  • This is massive progress! Very exciting stuff.

    Organisatiepagina weergeven voor IAMPS.

    771 volgers

    A turning point for non-animal approaches and safety assessment in Europe. The long-awaited EU Roadmap towards phasing out animal testing for chemical safety assessments has been released on June 1. Its objective is to “replace all animal testing for chemical safety assessments in the EU as soon as possible” through short, medium and long-term actions. IAMPS warmly welcomes this roadmap which, if implemented efficiently, can greatly accelerate the regulatory acceptance of microphysiological systems (MPS) and their impact in reducing animal use. 🔹The measures proposed in “Pillar 1: Making changes happen” such as the creation of regulatory exploration and safe spaces are especially appealing to MPS providers looking to engage more directly with regulators to explore how their models could contribute to the agencies’ needs. This approach will foster mutual understanding and alignment between developers, end users and regulators. 🔹Pillar 2 on “Keeping Europe at the forefront of research and innovation” highlights the need for a strong European industrial ecosystem to implement the roadmap with a clear ambition of global leadership in in-vitro biotechnologies. This is essential and, importantly, Europe can already rely on a mature and vibrant MPS industrial sector ready to scale up and support this transition. 🔹Pillar 3 focuses on change management and aims to create a Roadmap Steering Team to implement it. This team will include industry among other stakeholders and will interface with all regulatory agencies involved in the Roadmap. This brings an additional element of centralized, collaborative and focused coordination to implement non-animal methods in safety assessment across all agencies that was previously absent in the EU. This is excellent news and it reflects a strong policy commitment from the Commission. The roadmap is also, per se, a powerful economic signal to innovative industries, including the MPS sector. Organs-on-chips, organoids and other microfluidic platforms providers can now rely on a much more coherent and coordinated EU policy framework to develop and thrive. A lot of work still needs to be done to deploy MPS on a large scale in Europe, and significant and targeted EU funding will be required in the next Horizon programme to back the EU's ambition. But this is clearly a major turning point for safety assessment in Europe and the MPS industry. https://lnkd.in/dDSEpXQd AlveoliX, BiomimX® Srl, Dynamic42 GmbH, chiron, InSphero, MIMETAS, NETRI, React4life, TissUse GmbH.

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