Discovery of KT-474─a Potent, Selective, and Orally Bioavailable IRAK4 Degrader for the Treatment of Autoimmune Diseases

Interleukin-1 receptor associated kinase 4 (IRAK4) is an essential mediator of the IL-1R and TLR signaling pathways, both of which have been implicated in multiple autoimmune conditions. Hence, blocking the activity of IRAK4 represents an attractive approach for the treatment of autoimmune diseases. The activity of this serine/threonine kinase is dependent on its kinase and scaffolding activities; thus, degradation represents a potentially superior approach to inhibition. Herein, we detail the exploration of structure-activity relationships that ultimately led to the identification of KT-474, a potent, selective, and orally bioavailable heterobifunctional IRAK4 degrader. This represents the first heterobifunctional degrader evaluated in a nononcology indication and dosed to healthy human volunteers. This molecule successfully completed phase I studies in healthy adult volunteers and patients with atopic dermatitis or hidradenitis suppurativa. Phase II clinical trials in both of these indications have been initiated.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2024-08-16
DOI
https://doi.org/10.1021/acs.jmedchem.4c01305
Citations
49
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
13.84

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article

Discovery of KT-474─a Potent, Selective, and Orally Bioavailable IRAK4 Degrader for the Treatment of Autoimmune Diseases

Matthew M. Weiss, Kirti Sharma, Mike Sintchak, C. Browne et al.
49 citations
Journal of Medicinal Chemistry
Peptidase Inhibition and Analysis
13.84
article

Discovery of KT-474─a Potent, Selective, and Orally Bioavailable IRAK4 Degrader for the Treatment of Autoimmune Diseases

Matthew M. Weiss, Kirti Sharma, Mike Sintchak, C. Browne, Michele Mayo, Nello Mainolfi, Stephanie Skouras, Dirk Walther, Anthony Slavin, Nan Ji, Christine R. Klaus, Brad Enerson, Xiaozhang Zheng, Haoran Li, Yi Zhang, Guang Liu, Dapeng Chen, Yatao Shi, Xiao Zhu, Karen Yuan, Veronica A. Campbell, Alice McDonald, Haojing Rong, Ginny Massa, Xinbo Luo, Joe Kelleher
article en
49 citations

Abstract

Interleukin-1 receptor associated kinase 4 (IRAK4) is an essential mediator of the IL-1R and TLR signaling pathways, both of which have been implicated in multiple autoimmune conditions. Hence, blocking the activity of IRAK4 represents an attractive approach for the treatment of autoimmune diseases. The activity of this serine/threonine kinase is dependent on its kinase and scaffolding activities; thus, degradation represents a potentially superior approach to inhibition. Herein, we detail the exploration of structure-activity relationships that ultimately led to the identification of KT-474, a potent, selective, and orally bioavailable heterobifunctional IRAK4 degrader. This represents the first heterobifunctional degrader evaluated in a nononcology indication and dosed to healthy human volunteers. This molecule successfully completed phase I studies in healthy adult volunteers and patients with atopic dermatitis or hidradenitis suppurativa. Phase II clinical trials in both of these indications have been initiated.

Journal of Medicinal ChemistryVol. 67(20)
Woomera Therapeutics (US)
Sanofi
Zero hunger
Openalex Percentile: Top 1%
Peptidase Inhibition and Analysis
13.84
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