Cell And Gene Therapy For Enhanced CNS And Ocular Delivery In Nonhuman Primates

Early drug discovery, particularly with emerging modalities such as gene and cell therapies, presents unique challenges that require highly specialized delivery strategies and carefully selected preclinical models. Achieving precise administration to the intended anatomical target—whether in complex organs like the brain or eye—is crucial for evaluating therapeutic efficacy and safety.

In this webinar, we will explore essential methodologies and advanced techniques for delivering these innovative therapies with accuracy and consistency. We will discuss key considerations for optimizing drug administration, including selecting the appropriate delivery route, ensuring targeted biodistribution, and leveraging specialized animal disease models when necessary. Through real-world case studies, we will illustrate how these strategies have been successfully applied in preclinical research, shedding light on best practices for overcoming common hurdles in early drug development.

Join us to gain valuable insights into the cutting-edge approaches shaping the future of gene and cell therapy delivery, ensuring more effective and efficient translation from discovery to clinical application.