Resource Library

Discover Kymera’s research and resources on our exciting platform, pipeline, and additional cutting-edge technologies.

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Related Resources


December 9, 2024

Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of KT-333, a Targeted Protein Degrader of STAT3, in Patients with Relapsed or Refractory Lymphomas, Leukemia, and Solid Tumors

American Society of Hematology (ASH) 2024
cHL Liquid Tumors Solid Tumors
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December 9, 2024

Molecular Cancer Therapeutics: KT-253, A Novel MDM2 Degrader and p53 Stabilizer, Has Superior Potency and Efficacy Than MDM2 Small Molecule Inhibitors

Chutake, et al.
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October 25, 2024

Potent and Selective Oral STAT6 Degrader, KT-621, Inhibits IL-4 and IL-13 Functions in Human Cells and Blocks TH2 Inflammation In Vivo

American College of Allergy, Asthma & Immunology (ACAAI) 2024
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October 24, 2024

Predictive Markers of Response to the MDM2 Degrader KT-253

EORTC-NCI-AACR Symposium 2024
Liquid Tumors Solid Tumors
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October 23, 2024

CDK2 Heterobifunctional Degraders Co-Degrade CDK2 and Cyclin E Resulting in Efficacy in CCNE1-Amplified and Overexpressed Cancers

EORTC-NCI-AACR Symposium 2024
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October 23, 2024

The MDM2 Degraders KTX-049 and KT-253 are Highly Active in Wild-type TP53 Merkel Cell Carcinoma

EORTC-NCI-AACR Symposium 2024
Solid Tumors
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September 25, 2024

Potent and Selective Oral STAT6 Degrader, KT-621, Inhibits IL-4 and IL-13 Functions in Human Cells and Blocks TH2 Inflammation In Vivo

European Academy of Dermatology and Venereology (EADV) 2024
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August 16, 2024

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

Zheng, et al.
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July 29, 2024

Journal of Investigative Dermatology: Interleukin 1 Receptor–Associated Kinase 4 is Overexpressed in Hidradenitis Suppurativa Skin and Correlates with Inflammatory Biomarkers

McDonald, et al.
Hidradenitis Suppurativa (HS)
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June 26, 2024

Journal of Medicinal Chemistry: Discovery of KT-413, a Targeted Protein Degrader of IRAK4 and IMiD Substrates Targeting MYD88 Mutant Diffuse Large B-Cell Lymphoma

Weiss, et al.
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