Kymera Therapeutics Presents New Preclinical IBD Data for KT-579, a First-in-Class, Oral IRF5 Degrader, at Digestive Disease Week
Kymera Therapeutics presented new preclinical data at Digestive Disease Week showing its first-in-class oral IRF5 degrader KT-579 outperformed standard therapies in IBD models. The data demonstrated broad suppression of inflammatory cytokines and protection against weight loss comparable to JAK inhibitors and anti-TNF agents. The Phase 1 healthy volunteer trial for KT-579 is currently ongoing, with initial data expected in the second half of 2026. The study aims to confirm robust degradation of IRF5 at safe and well-tolerated doses.
Key figures
- Drug Name
- KT-579
- Phase Of Trial
- Phase 1
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