T1D Exchange pushes the boundary of the traditional research and development model by connecting the experience of living with T1D to the data about the disease. The result is a place where different perspectives are exchanged and faster progress can be made.
As a nonprofit facilitator we work to optimize T1D stakeholder clinical and research efforts by creating an integrated and patient-centric model with experts, data/evidence, samples, and patients comprising an end-to-end system to support the entire process of discovery to delivery.
Our integrated model puts people at the center of a comprehensive ecosystem with four key components: A Clinic Network of 70+ clinics across the US, a Clinic Registry with data from 26,000+ people with T1D, a Biobank housing a vast collection of biosamples, and Glu, the patient/caregiver online community. Together, these components accelerate the pace of research and discovery and improve patient care along the way.