
Autoimmune diseases affect approximately 15 million people in the U.S., representing 4.6% of the population. Current therapies rely on broad immune suppression that alleviates symptoms but carries long-term toxicity and increased infection risk. Biologics with improved selectivity are available for severe disease, but they do not halt progression and fail in up to 40% of patients. Emerging approaches may not induce durable effects or be applicable to many autoimmune diseases, or may rely on unproven delivery technologies or cumbersome manufacturing approaches.
We are building a pipeline of therapies designed to achieve disease-modification for patients with autoimmunity. Our thymus-targeted, bifunctional antibodies are designed to retrain the immune system to halt ongoing autoimmune attack while promoting the repair and restoration of healthy tissue. Our lead program, ZAG-101, is being developed for Type 1 diabetes, with additional programs advancing in autoimmune diseases of the gastrointestinal tract, skin, and nervous system.
