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Découvrir plus de posts
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Hung Trinh
AltruBio Raises $225M in Series B to Advance Ulcerative Colitis Candidate San Francisco-based biotech AltruBio has raised $225 million in an oversubscribed Series B round, the company announced Tuesday. The financing will help the company advance its ulcerative colitis candidate into mid-stage clinical trials. AltruBio’s candidate ALTB-268 is a first-in-class immune checkpoint enhancer (ICE) PSGL agonist antibody that is currently in a Phase IIa exploratory biomarker study in patients with biologic refractory ulcerative colitis (UC). The readout for the Phase IIa’s primary endpoint of clinical remission per modified Mayo score is expected sometime in the first half of next year. The Series B funds will support the trial and a Phase IIb study, which will have a primary endpoint of clinical remission in advanced therapy experienced and treatment naïve patients with moderate to severe UC. The biotech expects a readout in the second half of 2026. The Phase I data for ALTB-268 was encouraging as AltruBio reported positive topline data in August 2023. While the company initially gave no hard data points, the data supported the candidate’s progression into Phase II studies. “With this substantial investment, we are one step closer to bringing our first-in-class, novel immune checkpoint enhancer, ALTB-268, through our ongoing Phase IIa exploratory biomarker study and initiating an additional Phase IIb study while paving the way for potential indication expansion beyond ulcerative colitis,” AltruBio CEO Judy Chou said in a statement. https://lnkd.in/earF9qf7
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Tanya Nguyen, PhD
Committed to enabling you to #discovermore and #developfaster, we've released a new tool to support your discovery efforts: our searchable 𝐏𝐫𝐨𝐭𝐞𝐢𝐧 𝐀𝐬𝐬𝐚𝐲 𝐌𝐞𝐧𝐮: https://bit.ly/4cxI5tL How can you best use this interactive menu? 𝐃𝐢𝐬𝐜𝐨𝐯𝐞𝐫 #𝐁𝐢𝐨𝐦𝐚𝐫𝐤𝐞𝐫𝐬 𝐚𝐧𝐝 𝐏𝐫𝐨𝐭𝐞𝐢𝐧 𝐓𝐚𝐫𝐠𝐞𝐭𝐬 Peruse the full breadth of 12,000+ proteins and post-translational modifications (PTMs) we measure with our nontargeted #proteomics methods in your sample matrix of choice (plasma, cells, or tissue). See the coverage depth we can offer to assess proteome perturbations caused by disease processes or #drugresponse, and to profile differentially expressed proteins that may represent therapeutic targets. 𝐑𝐞𝐪𝐮𝐞𝐬𝐭 𝐚 𝐓𝐚𝐫𝐠𝐞𝐭𝐞𝐝 𝐀𝐬𝐬𝐚𝐲 𝐘𝐨𝐮𝐫 𝐏𝐫𝐨𝐭𝐞𝐢𝐧(𝐬) 𝐨𝐟 𝐈𝐧𝐭𝐞𝐫𝐞𝐬𝐭 If you have a specific protein to interrogate or target you're looking to modulate, you can easily search for it by name, UniProtID, or gene symbol. You can also filter the list for proteins associated with signaling pathways, biological processes, and a range of phenotypes to find those of relevance to probe for your study. Easily request these off-the-shelf, quantitative assays using the embedded forms. Get started here: https://bit.ly/4cxI5tL and don't hesitate to reach out to me if you have questions.
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LucidQuest
LucidQuest Strategic Insights (lqventures.com) >>> Gene&Cell Therapy >> Idorsia’s Jean-Paul Clozel retires as CEO, plots next steps; CRISPR Therapeutics nabs CMO from Sanofi: Jean-Paul Clozel → Jean-Paul Clozel is ready to pass the torch at his Actelion follow-up Idorsia, but he doesn’t want to walk away from the company altogether. Clozel will retire as CEO on June 13, and Idorsia has tapped his longtime lieutenant André Muller to replace him. The 69-year-old Clozel will now stand for election as chairman, while Mathieu Simon moves into the vice chairman post. The changes on the board don’t stop there. Jörn Aldag, Felix Ehrat and Peter Kellogg are stepping down, and Idorsia has nominated ex-Galapagos president Bart Filius. “It has been an absolute privilege to serve as CEO of Actelion and Idorsia for the past 24 years. I can think of no greater endeavor than discovering new medicines that help patients lead better lives,” Clozel said in a statement. “Having devoted so much energy to Idorsia, I want to stay engaged and support the company to realize its potential.” Muller was CFO at Actelion and followed Clozel to Idorsia as finance chief after J&J bought Actelion for $30 billion in 2017. Muller had a 17-year career at Pierre Fabre, where he was CFO from 2002-11. Idorsia has notched two FDA approvals in its seven-year history: insomnia med Quviviq and high blood pressure drug Tryvio. Naimish Patel → CRISPR Therapeutics has found a new medical chief and promoted one of its execs. Naimish Patel takes over as CMO from PK Morrow, who resigned on Jan. 26 and joined Takeda as head of the oncology therapeutic area unit. Patel quickly moved up to global program head for the megablockbuster Dupixent early in his tenure at Sanofi, where he was recently the head of global development in immunology and inflammation. Vertex’s Casgevy partner has also elevated Julianne Bruno to COO. She left McKinsey for CRISPR in 2019 and had been SVP and head of programs & portfolio management since March 2023. → Bavarian Nordic will be looking for a CMO after Laurence de Moerlooze’s departure at the end of the month. The GSK and Takeda vaccines alum succeeded Chris Heery as medical chief in the spring of 2020. “We have an operational setup that is robust enough for people to continue doing their jobs until a replacement is in place,” Bavarian Nordic CEO Paul Chaplin told MedWatch about the search. “They can manage that for six months or more, so I have no concerns at all.” Hanneke Schuitemaker → Meanwhile, at another vaccine developer, Valneva has welcomed Hanneke Schuitemaker as CSO. As J&J’s global head of viral vaccine discovery and translational medicine, Schuitemaker was involved in the development of vaccine candidates for Covid-19, HIV, RSV, Ebola and more. Valneva overcame a nearly two-and-a-half-month delay and received an… #lucidquest #genetherapy #celltherapy
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Nabil Arrach, Ph.D, MBA
Very Proud of Progenesis team. After hard work and group effort, It is my pleasure to announce the official launch of our High-Resolution Translocation Test. This is a single base resolution test that can distinguish between euploid and balanced translocation and detect small translocations (under 1MB) currently rejected with conventional PGT-SR. With this test, patients will increase their chance of having a successful pregnancy and reduce the risk of passing balance translocation and infertility to their kids. We are also launching Previda-Plus a test that can detect Triploidy, Haploidy, and Maternity/Paternity of embryos. This test will increase usability of 1pn, 3pn embryos and serve as a witness step for embryo transfer. #ivf #ivfjourney #infertility #ivfsuccess #ivfwarrior #ttccommunity #ivfcommunity #ttc #fertility #infertilityjourney #ivftransfer #ivftreatment #ivfstory #embryo #embryology #ttcsupport #reproductivehealth #fertility #infertility #pregnancy #fertilization Progenesis BrasilProgenesis India
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Ben Scruggs
In drug development, relying on outdated models can lead to missed opportunities for innovation and progress. A prime example is the continued use of Caco-2 cells for assessing intestinal absorption. While they have been a long-standing tool in the industry, it's time to recognize their limitations and explore more advanced alternatives. Here are three key reasons why Caco-2 cells fall short and why we should consider better options for more accurate and predictive results. 𝟭. 𝗟𝗮𝗰𝗸 𝗼𝗳 𝗖𝗼𝗺𝗽𝗹𝗲𝘅𝗶𝘁𝘆: Caco-2 cells originate from a single cell line, representing only one aspect of the intestinal epithelium. They lack the diversity and complexity of the human intestinal barrier, including the presence of various cell types such as goblet cells, enteroendocrine cells, and immune cells. This oversimplification can lead to inaccurate predictions of drug absorption and metabolism. 𝟮. 𝗗𝗶𝗳𝗳𝗲𝗿𝗲𝗻𝗰𝗲𝘀 𝗶𝗻 𝗘𝘅𝗽𝗿𝗲𝘀𝘀𝗶𝗼𝗻 𝗟𝗲𝘃𝗲𝗹𝘀: Caco-2 cells often exhibit different levels of transporters and enzymes compared to human intestines. This disparity can lead to incorrect predictions of drug permeability and interaction with transport proteins, potentially resulting in inaccurate assessment of a drug's bioavailability and pharmacokinetics. 𝟯. 𝗟𝗶𝗺𝗶𝘁𝗲𝗱 𝗣𝗵𝘆𝘀𝗶𝗼𝗹𝗼𝗴𝗶𝗰𝗮𝗹 𝗥𝗲𝗹𝗲𝘃𝗮𝗻𝗰𝗲: Caco-2 cells do not accurately mimic the full range of physiological conditions present in the human gut, such as pH variations, enzyme activity, and interactions with gut microbiota. This limitation can result in an incomplete understanding of how a drug behaves in the gastrointestinal tract. By moving beyond the status quo and embracing these advanced models, researchers can achieve more accurate and predictive results in drug development, ultimately leading to more effective and safer therapeutics.
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Dr Minshad Ali Ansari
Windfall Bio has secured $28m in Series A funding to further develop its methane-eating microbial. This investment from Amazon, B37 Ventures, and other partners is a testament to the company's vision of creating a more sustainable world. Who doubts that the Biocontrol market is not growing, especially microbial marbles for biofertilizers? Microbials can fix atmospheric nitrogen from 30-50kg Microbials can solubilise nutrients and make them ready for plants. Microbials can eat methane contributing towards CO2 reduction. Microbials can form a layer around the plant as Biofilm protecting roots and increasing resilience This investment shows the power of microbes Josh Silverman. Time is not far when these microbes can form a bigger part of fertiliser inputs and reduce their use in agriculture, making the soil more healthy. https://lnkd.in/dAhwQhqX
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iktos
🚨 Breaking news 🚨 iktos acquires SYNSIGHT, a life sciences technology company specializing in protein-protein and RNA-protein interactions-targeted drug discovery. As Yann Gaston-Mathe, CEO and Co-founder of Iktos comments « The acquisition of Synsight enables Iktos to expand its platform to new modulators of Protein-Protein interaction’s and RNA-Protein Interaction’s, historically highly challenging targets, thereby addressing major unmet medical needs in various therapeutic areas such as cancer and neurodegenerative diseases » The merger further complements Iktos' AI-based drug discovery platform, that currently includes generative AI design, Retrosynthesis, and AI-driven automated synthesis capabilities by adding the key step of automated biological testing thanks to MT Bench technology originally developed at INSERM. 👉 To learn more about this acquisition: https://lnkd.in/ez7hHmM8 #drugdiscovery #artificialintelligence #proteinproteininteractions #RNAinteractions Genopole Medicen Paris Region
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Santi Dominguez
A very nice application of #software to improve productivity in #chromatography #massspectrometry workflows by Mestrelab Research S.L. , part of the SciY family, with an excellent ROI as proven already by early adopter use cases #labautomation #laboratoryautomation #drugdiscovery #drugdevelopment
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Chris Lehman
April 18 and April 22, 2024 headlines from the Collabrity Report, a daily summary of financings for therapeutic biotechnology company executives and investors - www.collabrityreport.com New! Collabrity Report (CR) Analytics Metsera’s $290 Million Venture Financing Biohaven’s $230 Million Public Offering Zura’s $112 Million Private Placement Korro’s $70 Million Private Placement Corner’s $54 Million Series A Rubedo’s $40 Million Series A Benitec’s $40 Million Private Placement Salubris’s $35 Million Venture Financing Lirum’s $25 Million IPO Pathios’s $25 Million Series B Soligenix’s $5 Million Public Offering Neurenati’s $2 Million Seed Round NRx’s $2 Million Public Offering Bio-Path’s $1 Million Registered Direct Offering
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Shekhar Suman
🚀 Big News in Biopharma! 🚀 Profluent is making waves at the intersection of biotech and AI. Their innovative approach promises to revolutionize gene editing, and they're doing it with a bold move: open-sourcing their work! 🌐🔬 Introducing OpenCRISPR 🧬 Profluent's OpenCRISPR initiative is set to provide customizable gene-editing proteins designed entirely by AI. Imagine AI-generated CRISPR-like proteins that have never been seen before, capable of editing the human genome with unparalleled precision. 🔍 Highlights: AI-Powered: Trained on vast databases of protein sequences, Profluent's AI can generate hundreds of thousands of CRISPR-like proteins. OpenCRISPR-1: Their top-performing AI-created gene editor boasts 400+ mutations compared to CRISPR-Cas9, reducing off-target editing by 95% and keeping unwanted genetic changes below 1%. Why This Matters Attempting to edit human DNA with AI-designed systems is nothing short of a scientific moonshot. Profluent's success points to a future where AI can design bespoke cures for diseases, democratizing gene editing. 🔬 Real-World Impact: While AI-designed drugs have been in clinical testing for years, CRISPR tech just got its FDA green light last year with Casgevy for sickle cell disease and beta thalassemia. These treatments show the incredible potential of gene editing to transform lives. Open Collaboration Profluent invites researchers to test and provide feedback on OpenCRISPR-1. Their goal is to partner with top research institutions and drug developers to expedite the development of new genetic therapies, ensuring safe and ethical practices. Recent Milestones $35M Funding: Backed by Spark Capital, Insight Partners, Air Street Capital, and top angel investors from OpenAI, Salesforce, and Google. Join the Revolution This is a watershed moment in gene editing. Profluent is not just pushing the boundaries of what's possible; they’re opening the doors for global collaboration. Let's build the next generation of genetic medicines together! 👉 Read more and get involved: https://lnkd.in/gN9p-H6j #GeneEditing #CRISPR #AI #Biotech #OpenSource #Innovation #Profluent #HealthcareRevolution
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Ed Wallach
Vinod Khosla, founder of Sun Microsystems and Khosla Ventures “It’s better to try and fail, than fail to try”. Many times we are asked about the challenges of innovating in biotech from Patagonia and why we do it. There are many advantages of being in a place were talent wants to live, but beyond that, we know that turning Patagonia into a biotech powerhouse, can structurally change the society and living standards of our region. When so much good can be created, we rather try and fail, than fail to try. Kura Biotech Blikka Genomics by Kura Biotech SynBioBeta #PatagoniaBiotechHUB
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Lisa Krallis, MBA
An important topic with multiple posts and solutions to explore. Simulated data sets and data analysis are making it possible to derive insights faster and accurately in bioprocessing. Check out how the team at Culture has taken a deep dive on this subject by selecting the link in our post.
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Luis Barletta
🎉 Feedvax powers growth with annual distribution offerings of over $20 million! 🚀 At Feedvax, we are on a mission to revolutionize animal health and we are excited to share a milestone that validates our vision and technology. We recently closed a second distribution agreement, securing purchase commitments worth more than $20 million annually. 🤝💼 What does this mean? It is a huge vote of confidence in our innovative oral vaccine platform that is transforming the way farmers manage animal health. By eliminating the need for stressful animal handling we are unlocking unprecedented efficiency and welfare gains. And with these partnerships, we are poised to accelerate our global impact and market leadership. 🌍🥇 For our investors, this is an exciting validation of Feedvax's tremendous growth potential as we continue to expand our footprint reducing the $300 billion losses in the animal health industry due to diseases. 📈🔬 Thanks to all the FeedVax team, investors, and the people who support our growth every day. The future of animal health is simple, without stress and powered by Feedvax. 🚀 #Feedvax #AgTech #Sustainability #AnimalHealth #theendofanimalhandling
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Justin Goodarz
With protocols becoming more complex and the exclusion criteria stacking up, inherently, screen fail rates will increase. If participant 123 is not eligible for Study 1 at Site A, what tools/safeguards do you have in place to make sure participant 123 does not enroll in Study 1 at Site B just a few miles away? Verified Clinical Trials doesn't just prevent duplicate participants, we make sure your study is enrolling the MOST qualified participants based on their research history. This will pay dividends in the long run as you're weeding out professional participants who will damage the study in terms of retention, medication and/or ePRO adherence, etc. which ultimately delay study timelines, have effects on efficacy, and could even fail a study.
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