RNA Therapeutics Institute RNA Therapeutics From Concept to Clinic 2024

Description Include: 3 videos 1 pdf, size: 84.43 GB Target Audience: R&D scientists, CMC/quality leaders, translational and clinical teams, regulatory/strategy professionals, manufacturing/operations managers Sample video: contact me for sample video Information: A translational, bench-to-bedside program covering the full lifecycle of RNA medicines. Faculty connect platform science (siRNA, ASO, mRNA, saRNA) with delivery, CMC, regulatory strategy, and clinical development to help teams move candidates efficiently and safely toward approval. What You Will Learn Modality selection and design: siRNA vs. ASO vs. (sa)mRNA—chemistries, modifications, and stability Delivery systems: LNPs, GALNAc conjugates, polymers/peptides, local vs. systemic administration Preclinical translation: in vitro/in vivo models, PK/PD, biodistribution, immunogenicity and off-target risk CMC fundamentals: process development, analytics, release/stability testing, scale-up and tech transfer Clinical development: FIH design, dose selection, biomarkers, patient selection, endpoints, and safety monitoring Regulatory & quality: IND/IMPD packages, comparability, potency assays, pharm tox expectations, and risk management Manufacturing operations: raw materials (lipids, nucleotides, enzymes), single-use workflows, contamination control Data & tools: sequence optimization, secondary structure prediction, bioinformatics/AI for target and off-target assessment Access & value: manufacturing cost drivers, IP strategy, partnerships, and commercialization pathways Event Details Format: Case-based lectures, panel Q&A, and short technical workshops Structure: Concept/design → delivery/PKPD → CMC/manufacturing → clinical/regulatory → commercialization Takeaways: Checklists, study-design templates, and CMC/quality worksheets for immediate use Who Should AttendR&D scientists, CMC/quality leaders, translational and clinical teams, regulatory/strategy professionals, manufacturing/operations managers, platform and biotech founders, investors, and trainees entering the RNA space. Why Attend Replace trial-and-error with validated design and development playbooks Anticipate regulatory and manufacturing pitfalls early to de-risk timelines Bring back practical tools to align discovery, CMC, and clinical teams around the same plan   Topics: * Detail: