Exciting opportunity to join our clinical development team and help deliver on the impressive potential of off-the-shelf allogenic CAR Ts for patients with solid tumors like RCC. Let me know if you're interested or want to discuss further!
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Cordance Medical and EXACT Therapeutics have entered a strategic partnership to pioneer a new era in drug delivery to the brain. By integrating Cordance Medical's NeuroAccess™ platform, which enables non-invasive, targeted opening of the blood-brain barrier (BBB), with EXACT Therapeutics' Acoustic Cluster Therapy (ACT®) technology, the collaboration aims to enhance the efficacy and precision of drug therapies for patients with brain diseases, including tumors and neurodegenerative disorders. This partnership promises to revolutionize treatment options, making them more effective and accessible through upcoming clinical trials. #FocusedUltrasound, #PrecisionMedicine, #BloodBrainBarrier, #alzheimers, #braintumor, #drugdelivery https://lnkd.in/gWKdRcPQ
Cordance Medical and EXACT Therapeutics Announce Strategic Partnership to Revolutionize Drug Delivery to the Brain » Cordance Medical
cordancemedical.com
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Close molecular monitoring should be carried out to prevent HSPC hierarchical changes in patients with #myelodysplasticSyndromes enrolled in clinical trials involving venetoclax-based therapies. #MDS
Patients With MDS Receiving Venetoclax-Based Therapies Should Be Closely Monitored for Relapse - Hematology Advisor
https://www.hematologyadvisor.com
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Making the business of CGT commercially viable remains one of the critical challenges for therapy developers. Clinical success is apparent - why aren’t these therapies providing the financial results analysts and drug developers expect? The answer: It all comes down to reimbursement, operations of personalized medicine and cost. The author highlights commercial success for Yescarta and opportunities for other cell therapy providers. So kudos to Kite Gilead #kitegilead. We should all be optimistic that with the right focus we can enable patient access.
Biotech faces a reckoning: ‘We've lost our luster in cell therapies’
fiercebiotech.com
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The #FDA has granted ADDF-funded APRINOIA Therapeutics a fast track designation for APN-1607, a #PET tracer for imaging #tau protein in patients with progressive supranuclear palsy (PSP). This is a milestone for the field, helping enable #EarlyDetection and accurate diagnosis, which is crucial for treating patients with #neurodegenerative disorders like Alzheimer's and PSP. It will not only serve as the first tau imaging agent for PSP, but will add to the list of available tau imaging tools for #Alzheimers. The development of a vast arsenal of #biomarkers will play an integral role in the administration of #CombinationTherapy and #PrecisionMedicine care regimens that leverage each patient's unique biomarker profile to treat Alzheimer's on an individual basis. Read more about the news here: https://bit.ly/4dYARA6
APRINOIA Therapeutics Announces Fast Track Designation Granted by U.S. FDA to APN-1607 (florzolotau) for the Diagnosis of Progressive Supranuclear Palsy
https://aprinoia.com
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🔬 Exciting News: New Publication on Medrxiv 🌟 Peer review is ongoing, but I wanted to bring it to everyone's attention. 🎉 I'm thrilled to share our latest publication on Medrxiv! This study represents a significant advancement in our understanding of glioblastoma multiforme (GBM) treatment and its outcomes. 🧬 Background: Our research focused on the role of Aldehyde dehydrogenase-1A1 (ALDH1A1), a key enzyme in chemotherapy outcomes, particularly for the standard-of-care treatment, temozolomide, for GBM. Interestingly, we've found a correlation between high ALDH1A1 expression and poor prognosis across various cancers. 🤔 A pivotal discovery was the impact of Proton Pump Inhibitors (PPIs) – commonly prescribed for corticosteroid-induced gastrointestinal issues – as potential inducers of ALDH1A1, potentially affecting patient survival negatively. 📊 Methods: We delved into real-world data from 554 GBM patients, meticulously annotated from electronic medical records (EMR), as part of the XCELSIOR study. Our analysis, using a sophisticated time-varying Cox Proportional Hazard model, took into account various factors such as MGMT methylation status, patient demographics, and PPI use. 📈 Results: The data, spanning 225 cancer centers, revealed a noteworthy trend. Patients on PPIs generally showed a lower median overall survival (mOS) and 2-year survival rates. The effect was most pronounced in patients with MGMT-methylated GBM. 🚨 Conclusions: Our nationwide study strongly indicates the detrimental effects of PPIs on overall survival in GBM patients, especially those benefiting from SOC chemoradiotherapy. This raises critical concerns about the routine prescription of PPIs for managing chemotherapy-induced gastrointestinal toxicity. 🔑 Key Points: 🔑 Nationwide study signals potential risks of PPIs in GBM treatment. 🔑 Caution recommended in prescribing PPIs to GBM patients. 🔑 Prophylactic use of PPIs might elevate risk contrary to limiting chemo toxicity. 💡 Importance: This study sheds light on the unintended consequences of PPIs in GBM treatment, emphasizing the need for careful medication management. Our findings highlight the importance of re-evaluating standard practices to improve patient outcomes. 🔗 https://lnkd.in/gzQJdHJG #GBM #CancerResearch #MedicalPublication #ClinicalData #PatientCare #Medrxiv #HealthcareInnovation #Oncology #NeuroOncology
Proton pump inhibitors are detrimental to overall survival of patients with glioblastoma multiforme: results from a nationwide real-world evidence database
medrxiv.org
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If you are a glioblastoma patient, especially those who are mgmt methylated, and are taking a ppi, show this to your doctor. PPIs are used to prevent or treat stomach problems and include. Here's a list of some commonly used proton pump inhibitors (PPIs): 1. Omeprazole 2. Lansoprazole 3. Esomeprazole 4. Pantoprazole 5. Rabeprazole 6. Dexlansoprazole
🔬 Exciting News: New Publication on Medrxiv 🌟 Peer review is ongoing, but I wanted to bring it to everyone's attention. 🎉 I'm thrilled to share our latest publication on Medrxiv! This study represents a significant advancement in our understanding of glioblastoma multiforme (GBM) treatment and its outcomes. 🧬 Background: Our research focused on the role of Aldehyde dehydrogenase-1A1 (ALDH1A1), a key enzyme in chemotherapy outcomes, particularly for the standard-of-care treatment, temozolomide, for GBM. Interestingly, we've found a correlation between high ALDH1A1 expression and poor prognosis across various cancers. 🤔 A pivotal discovery was the impact of Proton Pump Inhibitors (PPIs) – commonly prescribed for corticosteroid-induced gastrointestinal issues – as potential inducers of ALDH1A1, potentially affecting patient survival negatively. 📊 Methods: We delved into real-world data from 554 GBM patients, meticulously annotated from electronic medical records (EMR), as part of the XCELSIOR study. Our analysis, using a sophisticated time-varying Cox Proportional Hazard model, took into account various factors such as MGMT methylation status, patient demographics, and PPI use. 📈 Results: The data, spanning 225 cancer centers, revealed a noteworthy trend. Patients on PPIs generally showed a lower median overall survival (mOS) and 2-year survival rates. The effect was most pronounced in patients with MGMT-methylated GBM. 🚨 Conclusions: Our nationwide study strongly indicates the detrimental effects of PPIs on overall survival in GBM patients, especially those benefiting from SOC chemoradiotherapy. This raises critical concerns about the routine prescription of PPIs for managing chemotherapy-induced gastrointestinal toxicity. 🔑 Key Points: 🔑 Nationwide study signals potential risks of PPIs in GBM treatment. 🔑 Caution recommended in prescribing PPIs to GBM patients. 🔑 Prophylactic use of PPIs might elevate risk contrary to limiting chemo toxicity. 💡 Importance: This study sheds light on the unintended consequences of PPIs in GBM treatment, emphasizing the need for careful medication management. Our findings highlight the importance of re-evaluating standard practices to improve patient outcomes. 🔗 https://lnkd.in/gzQJdHJG #GBM #CancerResearch #MedicalPublication #ClinicalData #PatientCare #Medrxiv #HealthcareInnovation #Oncology #NeuroOncology
Proton pump inhibitors are detrimental to overall survival of patients with glioblastoma multiforme: results from a nationwide real-world evidence database
medrxiv.org
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I am happy to announce that we have included our 200th evaluable patient in a first randomized-controlled clinical study evaluating a fully Electronic Patient File-integrated Model-Informed Precision Dosing (MIPD) application in kidney transplantation. The MIPD application is compared to physician-directed dosing of tacrolimus, a powerful immunosuppressive drug used as primary agent in de novo renal allograft recipients. After developing a PK learning model that included correlated within-patient variability and after successful in silico testing of the feedback dosing algorithm, a clinical study of 200 individuals (2:1 randomization) was predicted to have sufficient power to demonstrate differences in tacrolimus dosing precision and probability of target attainment (PTA)[CPT Pharmacometrics Syst Pharmacol. 2022 Mar;11(3):348-361 - https://lnkd.in/e4tfGD8x]. This trial was not primarily designed to show differences in early clinical endpoints after renal transplantation, but to assess MIPD performance (versus physicians) on tacrolimus PTA, dosing precision and user-functionality, reliability and safety of the application. Similar tailormade precision dosing algorithms have been developed for testing in lung and heart transplantation. Thanks for the enormous multi-disciplinary team effort to enable the development, set-up, execution and implementation of this study. An amazing team!
Predicting model-informed precision dosing: A test-case in tacrolimus dose adaptation for kidney transplant recipients - PubMed
pubmed.ncbi.nlm.nih.gov
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In drug discovery for osteoarthritis (OA), understanding the different phenotypes of the disease is crucial for developing targeted therapies. Overall, medical imaging plays a crucial role in phenotyping OA and guiding drug discovery efforts by providing insights into disease mechanisms, identifying therapeutic targets, patient recruitment, and evaluating the efficacy of potential treatments in preclinical and clinical studies. In this insightful paper, authored in collaboration with Dr. Olga Kubassova, IAG, IMAGE ANALYSIS GROUP President and Mikael Boesen, IAG's Therapeutic Area Lead for Rheumatic Diseases and Auto-Immunity, will delve into the topics of medical imaging, phenotyping, and more. https://lnkd.in/eZ4wGgfZ If you need medical imaging expertise to support your clinical trials, reach-out to me here on LinkedIn or at [email protected] Image Analysis Group is a leading imaging Clinical Research Organization (CRO) that blends medical and operational proficiency with state-of-the-art proprietary AI capabilities to drive drug development and facilitate the creation of potential companion diagnostic tools. Since 2007, IAG has been serving biotech and pharma clients globally, providing reliable support across all phases of imaging trials spanning multiple indications. Our team specializes in optimizing imaging studies by leveraging our in-house radiology expertise in trial design and execution, coupled with our cutting-edge Dynamika™ platform, which enables efficient imaging data management and accelerated patient recruitment. Through a pioneering innovation strategy, we enhance the value and market potential of novel therapeutic assets, as evidenced by successful pharmaceutical partnerships. #medicalimaging #osteoarthritis #OARSI #drugdiscovery #clinicaltrials #Cartilage
Osteoarthritis phenotypes and novel therapeutic targets
sciencedirect.com
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🚀 We are thrilled to announce the launch of Kidney Image Analysis Services via our cutting-edge NephroPath platform. Our AI-assisted image analysis services offer new and quantitative insights into renal pathology images, accelerating Chronic Kidney Disease (CKD) drug development studies. NephroPath’s AI-based quantification provides reproducible, consistent, and rapid scoring of renal pathology biomarkers. Compared to human assessments, it provides greater detail and precision. This can accelerate both preclinical and clinical development studies, as well as CKD biomarker discovery projects. For seamless implementation in ongoing projects, we provide comprehensive image analysis reports containing AI-based quantification findings, including biomarker scores and visual results. 🔗 Read the full story: https://lnkd.in/e8VRbDKz 🔍 Explore our kidney image analysis services: https://lnkd.in/eXtVwa6j #DigitalPathology #AIinPathology #KidneyHealth #DrugDevelopment
Aiosyn launches Kidney Image Analysis Services through its NephroPath platform to accelerate drug development studies - Aiosyn
https://www.aiosyn.com
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🚀 New Blog Post: https://lnkd.in/eWFXyZA2 "Navigating the Complexities of Opioid Antagonism: A Paradigm Shift in Dose Precision and Imaging."🌐 🔍 Our latest collaboration with esteemed co-authors brings forth groundbreaking insights into the world of opioid reversal. 🌎 Global Opioid Crisis: Meeting Challenges Head-on The urgency surrounding opioid drugs necessitates a paradigm shift in opioid antagonism. Fentanyl and carfentanil, potent opioids threatening public health, pose unique challenges due to their high opiate receptor affinity. Our latest research aims to address the intricacies of clinical reversal, emphasizing optimal dose precision and imaging. 📑 Pioneering Research: "Opioid Antagonism in Humans: A Primer on Optimal Dose and Timing for Central Mu-Opioid Receptor Blockade" Delve into our comprehensive study, leveraging decades of human opioid receptor imaging data. We've crafted a sophisticated pharmacokinetic algorithm, a powerful tool estimating receptor occupancy based on naloxone or naltrexone dosage. 💡 Advanced Dose Calculations: Shaping the Future of Opioid Antagonism Our pharmacokinetic algorithm empowers clinicians and researchers, offering refined tools for precise dose calculations. This revolutionary approach enhances clinical applications and research methodologies, ushering in a new era of opioid antagonism strategies. ⚙️ Tailored Precision: Optimizing Interventions Clinicians now have a refined toolkit, armed with precision in both dose and timing for central mu-opioid receptor blockade. In a landscape where every moment counts, our research equips them to navigate the complexities of opioid reversal with unprecedented accuracy. 🌐 Implications Beyond Academia: Shaping a Safer Future Our findings resonate beyond academic circles, promising a transformative impact on opioid antagonism understanding and management. Clinicians, researchers, and policymakers are invited to engage with the collective impact, contributing to more effective and targeted interventions. 👥 Join the Conversation: Explore the implications of our research and be part of the dialogue shaping a new era in opioid antagonism. 🚀 Let's redefine the landscape of opioid antagonism for a safer and healthier future! #OpioidAntagonism #DosePrecision #ResearchRevolution #biomolecularimaging
Clinical, Therapeutic & Diagnostic Imaging Consultants | BioMolecular Imaging
biomolecularimaging.com
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Vice President, Cell and Gene Therapy (CGT) | CAR T | TIL Therapy | Gene Therapy | Passionate Customer and Patient Champion
1yCongrats, John!! I missed that you had joined Allogene. Wishing you all the very best there. 🎉