Tag: Biopharmaceutical

  • CN Bio raises $21 million USD in first close of Series B investment round

    CN Bio raises $21 million USD in first close of Series B investment round

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    Bayland Capital and founding shareholder, CN Innovations Holdings Ltd, to invest $10 M and $5.5 M, respectively. Investment will expand product development and scaling of the organization to meet increased demand for Organ-on-a-Chip (OOC) solutions.

    Image Credit: CN Bio

    CN Bio, a leading provider of single- and multi-organ microphysiological systems, today announced it has raised a $21 million investment in the first close of its Series B fundraising round. The funding has been secured from several new investors; including $10 million from Bayland Capital, and $5.5 million from founding shareholder, CN Innovations Holdings Ltd. The investment will be used to accelerate the Company’s expanding product portfolio and to scale the business to support commercial expansion across key global markets.

    The global OOC market’s CAGR is estimated at 30.94%. This growth has been accelerated, in part, by the need for biopharmaceutical companies to improve the efficiency and success rate of innovative drug R&D and recent legislative changes, such as the US FDA Modernization Act 2.0. In response, CN Bio is delivering an ambitious expansion strategy to meet the increasing demand for its PhysioMimix® OOC technology and research services, and to provide deeper, clinically-relevant insights into early-stage preclinical drug discovery in a wider range of application areas, whilst reducing reliance on animal models. Over the past year, this has included a series of high-profile appointments to expand the Company’s leadership team in the UK and US, new product launches, and strategic industry collaborations. Notably, in December 2023, it was confirmed that PhysioMimix® OOC and its associated NASH ‘in-a-box’ kit provided critical human-relevant compound efficacy data for Inipharm’s INI-822, supporting regulatory approval to initiate clinical testing for metabolic liver disease – a pivotal inflection point in CN Bio’s development, and the broader industry.

    With the latest fundraising, CN Bio is well-positioned to continue its global expansion to meet the evolving needs of customers worldwide in key markets including toxicology, drug pharmacology and metabolic diseases. With 80% of clinical failures attributed to efficacy and toxicity issues, often derived from the poor predictiveness of animal and 2D cell culture models, the industry demand for OOC solutions in these areas is growing. By expanding R&D in the space, CN Bio will enhance the depth and breadth of tools and applications available to optimize drug discovery and development workflows, enabling researchers to generate data with greater predictability, lower risks of late-stage failures, and accelerate time-to-market for a wide-range of novel therapeutics.

    We are seeing pivotal growth across our industry, whereby drug developers are increasingly recognising the potential of OOC technology to augment, supplement and optimize their workflows.”

    Dr Paul Brooks, CEO, CN Bio

    He added: “We have strategically positioned ourselves accordingly to respond to the market needs and are proud to have received recognition from our major shareholder, CN Innovations, and new institutional investors such as Bayland Capital, to drive this vision forward. The investment is a testament to our team’s hard work and dedication to best supporting our customers to bring drugs to patients more quickly, more cost-effectively, and through less animal experimentation.”

    Yuexing Su, Founding Partner, Bayland Capital, commented: “OOC technology is an exciting market with compelling opportunity for growth. CN Bio has taken key steps to build a team with extensive industry expertise and robust networks across the industry, with a longstanding track record of success. We look forward to the continued success for the Company as it further capitalizes on this unique growth opportunity and delivers on its future expansion plans to remain at the cutting-edge of the field. We will leverage our networks and shareholders’ base to further support and cement the leading position of CN Bio in OOC development.

    Charles Chong, Managing Director, CN Innovations, added: “We are encouraged by CN Bio’s ongoing success and, in particular, the team’s achievements over the past years, during which conditions have been difficult in the broader economy. In this time, key milestones have been met, not just for the Company, but also the wider industry – including CN Bio providing critical human-relevant compound efficacy data to support the FDA’s approval for Inipharm’s Phase 1 clinical trial for metabolic liver disease. We are pleased to be supporting CN Bio again as it looks ahead and strengthens its future growth plans, of which, expanding its product portfolio in markets that hold huge impact for the industry, such as metabolic disease modelling and toxicology, will be key.”

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  • Sapio Sciences launches new multimodal registration capabilities for its lab informatics platform

    Sapio Sciences launches new multimodal registration capabilities for its lab informatics platform

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    Sapio Sciences, the science-awareTM lab informatics platform, today announced the launch of its new multimodal registration capabilities. This new functionality unifies small-molecule, large-molecule, and multimodal discovery workflows, including entity registration, on a single platform.

    With these latest features, Sapio is helping R&D teams overcome the collaboration and efficiency challenges traditionally associated with the development of multimodal therapies and products.   

    New modalities, such as recombinant proteins, peptides, and engineered antibodies, are key drivers of biopharmaceutical industry growth. According to BCG, revenues from new-modality products increased by $60 billion over the past few years, while revenues from conventional products declined by $10 billion.

    Furthermore, BCG projects that the percentage value of new modalities in the five-year forward pipeline between 2019 and 2023 will increase from 41% to 56%, far outpacing conventional ones.

    “The days of viewing drug discovery through the separate lenses of small molecules and large molecules are outdated,” said Kevin Cramer, president and CEO of Sapio Sciences. “Today, drug discovery in biopharma is increasingly multimodal, and leading-edge laboratories require a single unified informatics platform that supports small-molecule, large-molecule, and new modality discovery workflows, including registration.”

    Today, companies typically use separate registration systems, one for small molecules and another for large molecules. For multimodal discovery, separate registration becomes problematic. A unified registration system solves this by enabling researchers from diverse departments, such as chemistry and molecular biology, to work together on new modalities seamlessly, manage all data in one place, have one system for regulatory compliance, and collaborate with a single source of truth.

    The foundation of the Sapio Platform is a single materials management system that does not distinguish between small-molecule, large-molecule, or multimodal entities — rather, they are all collected and managed as molecular materials with attributes that record the unique characteristics of each type of entity.

    Uniquely, Sapio also connects its sample management with registered entities for seamless data visualizations and traceability.  As a result, chemists and biologists can work together on a single, unified drug discovery platform that combines Sapio LIMS™, Sapio ELN™ and Sapio Jarvis™ to integrate and harmonize collective scientific data across the laboratory informatics enterprise.

    New biotech ventures will want to adopt the Sapio Platform now to address leading-edge new modality drug discovery opportunities and position themselves for accelerated discovery and insights from day one.

    Established biopharma enterprises will want to reassess the limitations and risks of currently deployed separate chemistry- and biology-centric informatics and evaluate the benefits and advantages of a single unified lab informatics platform from Sapio to optimize leading-edge multimodal drug discovery.

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  • Ubiquigent and Debiopharm enter agreement to support USP1 inhibitor programme for Debio 0432

    Ubiquigent and Debiopharm enter agreement to support USP1 inhibitor programme for Debio 0432

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    Ubiquigent Limited (Ubiquigent), a drug discovery and development company harnessing novel deubiquitinase (DUB) modulators as new therapeutics for areas of high unmet medical need, today announced an agreement with Debiopharm, a biopharmaceutical company aiming to develop tomorrow’s standard-of-care treatments to cure cancer and infectious diseases. The agreement will support the development of Debiopharm’s USP1 inhibitor programme, Debio 0432.

    Under the terms of the agreement, Ubiquigent will deploy its DUB-focused platform, combined with its deep understanding of the DUB field, to develop novel target engagement assays to support Debio-0432 as it approaches the clinic.

    Currently, in late-stage preclinical development, Debio 0432 is a small molecule with best-in-class potential that could be deployed to combat multiple tumour types. Through its potent and selective inhibition of USP1, a critical player in the DNA damage repair (DDR) pathway, Debio 0432 has the potential to induce synthetic lethality in tumour types with underlying defects of DNA repair genes.

    We are delighted to enter this agreement with Debiopharm, supporting the development of its advanced USP1 inhibitor programme. Following our successful collaborations with other clinical stage companies, this latest agreement further demonstrates the capability of Ubiquigent’s platform to address all aspects of DUB drug discovery and development, encompassing target validation, hit-to-lead, candidate selection, translational research, and the development of assays to support clinical evaluation.” Jason Mundin, CEO of Ubiquigent, said: “With multiple assets now reaching clinical stage, we look forward to seeing the continued progression and expansion of the DUB field over the coming years as more companies enter the space and new therapeutics enter the clinic.”

    Bertrand Ducrey, CEO, Debiopharm, commented: “Ubiquigent’s specialised drug discovery platform is uniquely positioned to support our USP1 inhibitor programme as it approaches the clinic, enabling the development of novel target engagement assays. Selective inhibition of USP1 to interrupt DNA damage repair pathway is an exciting approach to cancer treatment.”

    To learn more about Ubiquigent’s platform for DUB-focused drug discovery, visit: https://www.ubiquigent.com/platform

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