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EP 053 Industry Insights - Breaking the Curse of Huntington's Disease Uniqure's AMT 130 Treatment скачать в хорошем качестве

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EP 053 Industry Insights - Breaking the Curse of Huntington's Disease Uniqure's AMT 130 Treatment

EPISODE 053: "Breaking the Curse of Huntington's Disease - AMT-130's Historic 75% Disease Slowing" GENE THERAPY | Huntington's Disease Treatment | RNA Interference | Pharmaceutical Manufacturing | Neurodegenerative Disease | AAV Vector Delivery Discover how UniQure's AMT-130 gene therapy achieved a groundbreaking 75% slowing of Huntington's Disease progression, marking a turning point for genetic medicine. This episode explores the renaissance of gene therapy after industry setbacks, the innovative RNA interference technology saving lives, and how cloud-based manufacturing systems are scaling these life-changing treatments from lab bench to global distribution. KEY TOPICS COVERED: Huntington's Disease Science • The genetic curse: CAG repeat expansion affecting 41,000 Americans and 200,000 at-risk carriers • How toxic huntingtin protein destroys brain neurons and disease progression timeline • 50/50 inheritance pattern and symptom onset during prime life years AMT-130 Gene Therapy Breakthrough • 75% disease slowing in clinical trials with one-time brain injection • AAV5 viral vector delivering microRNA to silence huntingtin mRNA permanently • FDA Breakthrough Therapy designation; BLA planned Q1 2026 • 8.2% reduction in neuronal death biomarkers Gene Therapy Technology & Industry • RNA interference mechanism and why AMT-130 succeeds where others failed • Bluebird Bio rebirth as Genetix Biotherapeutics; Sarepta's Elevidys lessons • 30+ siRNA/miRNA clinical trials; 40% increase in RNA therapeutics patents • $2.3 billion Q1 2025 venture capital investment Manufacturing Revolution • Cloud-based MES systems enabling gene therapy scale-up • Tempo Manufacturing Cloud: real-time monitoring, AI optimization, multi-site consistency • Reducing costs from millions to hundreds of thousands per dose • Quality control and release by exception cutting weeks off availability Patient Impact & Future Vision • What 75% slowing means: decades of preserved independence and quality of life • Expansion to other genetic diseases and presymptomatic treatment potential • 2026-2040: CRISPR editing, distributed manufacturing, preventive genetic medicine • Vision: Huntington's as a prevented disease by 2040 Perfect for: Pharmaceutical manufacturing professionals, biotechnology researchers, neurology specialists, healthcare innovation leaders, regulatory affairs professionals, genetic counselors, and anyone interested in precision medicine. Featured Companies: UniQure | Genetix Biotherapeutics | Sarepta | Roche | Ionis | Northwestern Medicine | Apprentice.io Tempo Manufacturing Cloud Host: Frank Maggiore | Series: Apprentice.io Industry Insights Podcast #GeneTherapy #HuntingtonsDisease #RNAInterference #Pharmaceutical #Biotechnology #PrecisionMedicine #AAVVector #AMT130 #Manufacturing #CloudMES #FDAApproval #RareDisease #GeneticMedicine #BioManufacturing #HealthTech #Neuroscience #MedicalBreakthrough #GMPManufacturing #FutureOfMedicine ENGAGE WITH US: Like, comment, subscribe for weekly science-based pharmaceutical insights. Share with colleagues in pharma and biotech. Learn more: apprentice.io Disclaimer: The content in this video podcast is for informational purposes only. The views and opinions expressed are those of the speakers and do not necessarily reflect the official policy or position of Apprentice.io or any other agency, organization, employer or company. This podcast does not constitute medical, financial, regulatory, or legal advice. Viewers should consult with appropriate professionals for specific advice. Apprentice.io makes no representations or warranties of any kind, express or implied, about the completeness, accuracy, reliability, suitability or availability of the information contained in this video. Any reliance you place on such information is strictly at your own risk. Related Topics: viral vector production, cell and gene therapy manufacturing, antisense oligonucleotides, fecal microbiota transplantation, CRISPR gene editing, metabolomics, metagenomics, live biotherapeutic products, bioreactor optimization, process analytical technology, digital transformation pharma, genetic testing, immunotherapy, clinical trial design, regulatory strategy, breakthrough therapy designation

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