Gate2Brain aims to enhance patients’ quality of life by offering a technology that improves drug transport effectiveness while minimizing side effects. Through extensive testing in rodent, we have confirmed the efficacy and safety approach and now poised to transition to non-rodent models, bringing us closer to human application in clinical trials.
Our technology exhibits several key advantages, including protease resistance across various species, the ability to transport a diverse range of cargoes, low production costs, and minimal immunogenicity. By overcoming societal and economic barriers, we strive to make medicines accessible to all, particularly paediatric patients worldwide.
A significant milestone in this direction is the optimization and patenting of a cost-effective scale-up manufacturing process, paving the way for an affordable treatment option while the potential to impact paediatric patients globally.
In essence, Gate2Brain offers a groundbreaking delivery technology that enables non-invasive, non-antigenic, permeable, stable, soluble, and receptor-specific drug transport across the blood brain barrier (BBB) and into the central nervous system (CNS), positioning us on the path to clinical trials.
To expedite this journey to patients, we are actively addressing regulatory considerations, including seeking Orphan Drug Designation (ODD) for G2B-002 and engaging with the European Medicines Agency (EMA) through Scientific Advice. Additionally, we are strategizing our approach to market access for G2B-002 to ensure its availability and affordability for those in need.