Small Molecule Orphan Drugs: Status Quo, Challenges, and Perspectives
Summary: In this webinar, experts discuss the key drivers and challenges of orphan drug development and manufacturing.
Better Decisions for Phase 1 Clinical Trials Using Integrated Design Models
Summary: Learn how innovative trial designs, on-demand manufacturing, real-time clinical data-based dose adjustments, and partnering with experienced formulators and Contract Research Organizations (CROs) can enable faster, better decision making during phase 1 clinical trials.
Current State & Challenges of Phase 1 Oral Small Molecule Drug Development & Outsourcing
Summary: A recent survey explored the attitudes and changing perceptions of experienced Phase 1 development professionals toward development challenges and available solutions.
Webinar: ADC’s Are Back Stronger Than Ever: How, Why & What’s Next
Summary: Mike Riley, President, Catalent Biologics, will discuss the latest trends in ADC discovery and development, with a focus on how next generation pipelines are being shaped by payload and linker chemistry innovations, including those from Catalent’s award-winning SMARTag® ADC platform.
Optimizing the Path from Pre-Clinical to Clinical Development
Summary: In this eBook, learn more about how the timely progression of a drug candidate into clinical trials is critical for pharmaceutical companies seeking to bring new products to the market.
Plasmid DNA and Advanced Therapies: Accelerating Path to Clinic
In this webinar experts will discuss the challenges cell and gene therapy innovators face and how experts resolve these barriers through adopting technology and strategy that drive an optimized plasmid production process and supply.