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KTX-582

Development stage
Preclinical
Lead developer
Kymera Therapeutics
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
Administration
Oral
01

Overview

KTX-582 is an investigational **oral small-molecule proteolysis-targeting chimera therapy** developed by **Kymera Therapeutics** for **MYD88-mutant diffuse large B-cell lymphoma** and related B-cell malignancies. It is designed to induce targeted degradation of **interleukin-1 receptor-associated kinase 4** and the IMiD substrate **Ikaros**, producing dual suppression of innate immune signaling and lymphoid transcriptional programs. Preclinically, KTX-582 has shown potent degradation activity, induction of apoptosis in MYD88-mutant DLBCL cell lines, and tumor regressions in lymphoma models, supporting its positioning as a targeted antineoplastic degrader program.

02

Targets

IKZF1 (Ikaros family zinc finger protein 1)IKZF3 (Zinc finger protein Aiolos)IRAK4 (Interleukin-1 receptor associated kinase 4)

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