Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
KT-295 is an investigational, first-in-class, once-daily oral small molecule degrader of tyrosine kinase 2 (TYK2), a member of the Janus kinase (JAK) family required for Type I interferon (IFN), interleukin-12 (IL-12), and interleukin-23 (IL-23) signaling. Developed by Kymera Therapeutics, KT-295 is designed to selectively degrade TYK2 protein, thereby blocking key inflammatory pathways implicated in autoimmune and inflammatory diseases. Preclinical studies have shown that KT-295 can replicate the human genetic loss-of-function profile of TYK2 and block these pathways similarly to upstream biologics. The drug aims to deliver biologics-like efficacy in an oral formulation for diseases such as inflammatory bowel disease (IBD), psoriasis, psoriatic arthritis, and systemic lupus erythematosus. As of early 2025, it is advancing toward Phase 1 clinical trials in healthy volunteers[1][3][4][5][6][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on KT-295.