🌾 𝗪𝗵𝗲𝗮𝘁'𝘀 𝗪𝗲𝗲𝗸𝗹𝘆!! 🌾 𝗕𝗿𝗲𝗮𝗸𝗶𝗻𝗴 𝗡𝗲𝘄𝘀! 🤜 Enveric Biosciences, Inc. has completed manufacturing of drug material enabling the completion of preclinical work for EB-373 and all the related studies. 🤜 GeneFab sublease Senti Biosciences cGMP facility for $38 Million and Philip Lee becomes CEO. 💊 🧬 𝗠&𝗔 𝗼𝗳 𝘁𝗵𝗲 𝘄𝗲𝗲𝗸! 🤜 Willow Biosciences Inc partner with biopharma firm to develop more sustainable pharmaceutical ingredients which reduce cost and create less waste. 🤝💼 𝗘𝘅𝗽𝗮𝗻𝘀𝗶𝗼𝗻 𝗼𝗳 𝘁𝗵𝗲 𝘄𝗲𝗲𝗸! 🤜 Akari Therapeutics, Plc opens HQ in Boston to support their current expansion of the US operations for phase 3 clinical trials of nomacopan in paediatrics. 🏭🌎 𝗜𝗻𝘃𝗲𝘀𝘁𝗺𝗲𝗻𝘁 𝗼𝗳 𝘁𝗵𝗲 𝘄𝗲𝗲𝗸! 🤜 LEO Pharma acquire Timber Pharmaceuticals, Inc. for $36 Million, a $14 Million upfront payment and $22 Million in contingent value rights if hit certain milestones. 🤑💰 𝗡𝗲𝘄 𝗟𝗲𝗮𝗱𝗲𝗿𝘀𝗵𝗶𝗽! 🤜 Particle Dynamics name Anish Parikh as CCO, he brings 25 years experience across commercial and R&D sectors for multiple key CDMO's. 🤜 Wheeler Bio, Inc. names Marc Helouin Chief Quality and Regulatory Officer, bringing in 25 years experience in biopharma across multiple domains. 👨🔬👩🔬 Did I miss anything, let me know in the comments! 👇 #pharma #biotech #cdmo #drugdevelopment #drugmanufacturing #lifescience
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📚 Recently delved into "The Billion Dollar Molecule" by Barry Werth, which offers a riveting journey into the early days of Vertex Pharmaceuticals. What struck me most was the company's pioneering spirit in championing structure-based drug design (SBDD), marking a competitive advantage through methodology. Instead of sifting through thousands of natural compounds hoping one would work, they harnessed the power of detailed chemical knowledge and molecular modeling to craft drugs tailored for specific biological targets - akin to crafting a key meticulously designed for a particular lock. This transformative approach underscores the notion that biopharmaceutical innovation isn't just about discovery but also about the methodologies we embrace. It is a must-read for those passionate about the future of medicine and the strategies that drive it forward. #BookRecommendation #Biopharma #Pharma #Innovation #Biotech ⚗ 🔬
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How can I leverage the technology investments I've already made? How can I implement them in the least disruptive way possible? In the competitive world of biotech and pharmaceuticals, pipeline programs are crucial for successful drug development. However, without a well-planned strategy, you risk wasting time, and capital. It's time to create a roadmap to success. At Aspen Biosciences, we recognize the challenges of scaling up drug discovery programs. Whether your team is new to the process or seeks to increase the number of investigational new drug (IND) submissions annually, our Roadmap Service can guide you towards success. We formalize the planning process, establishing a repeatable approach adaptable to various indications, modalities, and infrastructures. Our step-by-step roadmap identifies areas for improvement and scalability, ensuring your scientific goals are met efficiently and effectively. Our support doesn't end with planning; we offer comprehensive assistance for a smooth transition. Our experienced team can develop software tools or advise on addressing gaps revealed during the process. With years of expertise in pharmaceutical and biotech drug discovery, we know how to harness technology and specialized tools for maximum productivity. ✉️[email protected] #biotech #pharma #drugdiscovery #AspenBiosciences
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How can I leverage the technology investments I've already made? How can I implement them in the least disruptive way possible? In the competitive world of biotech and pharmaceuticals, pipeline programs are crucial for successful drug development. However, without a well-planned strategy, you risk wasting time, and capital. It's time to create a roadmap to success. At Aspen Biosciences, we recognize the challenges of scaling up drug discovery programs. Whether your team is new to the process or seeks to increase the number of investigational new drug (IND) submissions annually, our Roadmap Service can guide you towards success. We formalize the planning process, establishing a repeatable approach adaptable to various indications, modalities, and infrastructures. Our step-by-step roadmap identifies areas for improvement and scalability, ensuring your scientific goals are met efficiently and effectively. Our support doesn't end with planning; we offer comprehensive assistance for a smooth transition. Our experienced team can develop software tools or advise on addressing gaps revealed during the process. With years of expertise in pharmaceutical and biotech drug discovery, we know how to harness technology and specialized tools for maximum productivity. ✉️[email protected] #biotech #pharma #drugdiscovery #AspenBiosciences
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💥 The Need for a Leaner, More Agile Biotech Ecosystem The pharmaceutical industry, boasting revenues over $1.3 trillion in 2020, is grappling with R&D inefficiencies. Often, even insiders lack clarity on their own R&D costs. The opaque nature of traditional R&D in big pharma makes efficiency comparisons challenging. A shift towards a more transparent, agile biotech system is essential. 🌟 Enter Vesper: our biotech venture is dedicated to fostering a nimble biotech ecosystem. We achieve this by integrating cutting-edge technologies, and collaborating with academic groups for deeper industry insights. By prioritizing innovation and agility, we're paving the way for a more efficient and responsive biotech future. #biotech #agility #Vesper https://lnkd.in/gsE7fEBM.
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October 11, 2023 🤝Great Bay Bio and MNC Kickstart Strategic Cooperation for AI-Driven Cell Culture Media Development Great Bay Bio, a pioneering AI-enabled biotechnology company, and a renowned multinational corporation (MNC) in the life science industry have officially launched a strategic cooperation centered around AI-driven cell culture media development. Based on the powerful development capabilities of GBB's AI-enabled culture database platform (AlfaMedX®) and the value and management of MNC's global supply chain, this project will provide more high-quality media products and solutions for numerous biopharmaceutical companies worldwide, helping to improve the resilience of the global culture media industry chain. The collaboration will encompass technology platform access, out-licensing, and royalty fee distribution based on global sales of media formulas, thereby enhancing both the MNC's competitive edge and service capabilities. This partnership will also enable GBB to participate in the cell culture media development, optimization processes and the cell culture media supply at various stages of drug R&D, leveraging the MNC’s extensive bioprocessing expertise. For more info, please refer to https://lnkd.in/gBayjdHj. #GreatBayBio #GBB #MNC #culturemedia #cellline #cooperation #collaboration #lifescience #collaboration #biopharmaceutical #bioprocessing #biotechnology #development
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Congratulations to Peregrion a brand new new startup from TNO! TNO spent ten years developing a breakthrough in biomedical technology, leading to the regulatory acceptance of Accelerated Mass Spectrometry (AMS) technology. This advancement is now the foundation of Peregrion, a new spin-off aimed at enhancing early clinical drug development for pharmaceutical companies. Peregrion, the 41st company to spin off from TNO’s Tech Transfer initiative, uses AMS technology for microtracer studies. This method promises to make drug development faster and safer, a critical advancement for the pharmaceutical industry. ‘We are very proud at TNO that our 10 years of pre-competitive research proves that it is still possible to generically improve the drug development process.’ Peter van Dijken -Managing Director of TNO Healthy Living and Work Looking forward to seeing your startup grow Wouter Vaes (CSO/Co-Founder Peregrion) & Steven Erpelinck (CCO/Co-Founder)! ‘We have clearly managed to position the microtracer approach as one of the most promising animal-free innovation trajectories. Moreover, we have now reached to point that the global pharmaceutical industry is embracing our technology to implement the ‘human first, human only’ strategy as the preferred method to obtain drug metabolism data, from a scientific as well as a business perspective.’ - Wouter Vaes ‘TNO positions Peregrion to further build on the AMS technology that we developed, offering the ideal setting to support clients in the pharmaceutical industry with bringing the best medicines to patients earlier.’ - Steven Erpelinck As Peregrion sets out to build their startup, Leiden Bio Science Park is eager to play a supporting role in its journey wherever we can. Our park in Gemeente Leiden and Gemeente Oegstgeest is known for fostering growth and innovation among startups, offering a rich network of research institutions and companies. This environment not only supports startups but also accelerates the translation of research into practical solutions. Would you like to explore the LBSP? Start a conversation! #massspectrometry https://lnkd.in/d9Sm4E9u
TNO launches Peregrion to bring science to the marketplace
tno.nl
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In today’s Data-Driven Biotech Mondays, I’d like to spotlight a Charles River Laboratories site in Hungary. Charles River, a CRO, offers a range of services to the pharmaceutical industry, with this particular highlight focusing on small molecules projects. A critical safety measure during the ADME/Tox screening phase is the assessment of drug transporter inhibition. The objective is minimal inhibition to prevent potential toxic events. This consideration extends beyond the drug in question, as drug-drug interactions become significant in a more comprehensive evaluation of drug transporters. The process is tedious, time-consuming, labor-intensive, and costly due to the extensive number of sampling points required. So Charles River teamed up with TetraScience to address the challenge. They invested 5 months into updating their data management and preparation efforts, and trained a model is order to reduce the time and cost. Ultimately they were able to produce a model that improved their calculation accuracy and reduced the necessary sampling points in half. As the project matures, they anticipate a 50% reduction in lab experiments per drug. The sampling reduction is for sure notable, but I believe that the true value lies in the data systems built, which can be repurposed not only for this project but for future innovations as well! ========= Want to hear about more use cases like this, or have one you’d like highlighted? DM me or comment
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We ABSOLUTELY need the for-profit private sector to be the solution - NO ONE ELSE has the risk capital, research & development, supply chain, regulatory and stewardship capabilities to succeed on the global scale. 🧵 The Biopharma Industry holds the key. Biopharmaceutical companies have a crucial role to play in the fight against AMR. No-one else has the risk capital, research & development, supply chain, regulatory and stewardship capabilities to succeed on a global scale. But the need to limit antibiotic use and the uncertainty around reimbursement has limited larger companies’ investment in this area. Today most innovation is driven by universities and small, under-resourced biotech companies, which account for 95% of the new antibiotics in research and development. Tell us what you think! #StopSuperbugs #AMR #AntimicrobialResistance
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The breakthrough of #GenerativeAI was a turning point for #pharma and #biopharma - changing the way medicines are discovered, developed, and delivered. 🔄 Hear from our CEO Raj Indupuri on why this advancement was the most consequential event of 2023 and how its impact will drive what's next for #ClinicalTrials, in Pharma's Almanac: https://lnkd.in/da3fd6kj
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The 2024 Pharmaceutical Innovation and Invention Index is live! We are proud to publish this year's indices: the 13th year of analysing innovation and invention in our industry. https://lnkd.in/e_b_TtCY The question, 'if you give the same molecule to two companies in phase I, would they be equally successful?' remains a defining one. The answer is clearly 'no,' so the more interesting question is 'why'?'—perhaps one of the most important questions for our industry. When we first asked ourselves that question, more than a decade ago, it followed a more soul-searching one: ‘what if we're wrong?’ A healthy question, but not one that is typical of consultancies. Understanding how companies create value from their pipelines means being open to novel and multiple approaches - we produce this Index so that we know what we’re talking about when we talk about pharmaceutical innovation. If you like, we’re ‘following the science’ rather than assuming we’re right.
Transforming Strategy At Phase II | IDEA Pharma
ideapharma.com
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