Company

Our mission is to revolutionise drug and therapeutic discovery and development, provide a novel and affordable solution for medical treatment, patient stratification and disease diagnostics for rare diseases in newborns.
We have noticed a lack of effective treatments for these conditions and an urgent need for human organ proxies in vitro for disease modelling, biomarker, drug and therapeutic discovery.
To address these challenges, we will provide state-of-the-art and first-in-class human disease organoids for personalised precision medicine, regenerative medicine and preventive care for rare newborn diseases. Our organoid platform marks the beginning of the deployment of a novel and affordable solution for medical treatment, patient stratification and disease diagnostics. This platform is poised to make a significant impact in reducing mortality rate, saving billions of dollars in healthcare costs and improving the quality of life for individuals.

Description

GLOAS (Gut Liver Organoid Advance Science) Limited – a pioneer in revolutionising drug and therapeutic discovery and development

Our human iPSC-derived organoids provide an immediate solution to the problem.

An organoid is a miniaturised and simplified version of an organ produced in vitro in three dimensions, demonstrating realistic micro-anatomy and resembling a near-native mini-organ in a dish. They are derived from tissue stem cells, embryonic stem cells, or induced pluripotent stem cells (iPSCs), which can self-organise in three-dimensional culture due to their self-renewal and differentiation capabilities. Scientists use organoids to study diseases and treatments in the laboratory.

GLOAS offers state-of-the-art technology platforms, including patient and normal human induced pluripotent stem cells (hIPSCs); first-generation patient and normal hIPSC-derived human organoids with one cell type (human organoids 1.0); second-generation advanced patient and normal human organoids with multiple cell types (human organoids 2.0); tissue hydrogel; and fabricated human bile ducts, all aimed at revolutionising the discovery and development of drugs and therapeutics for neonatal rare diseases.