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BioWorld - Monday, March 30, 2026
Home » Topics » Drugs » Degradation inducer

Degradation inducer
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Neurology/psychiatric

Captor Therapeutics patents new Nek7 degradation inducers

Nov. 25, 2025
Captor Therapeutics Inc. has disclosed molecular glue degraders comprising a cereblon (CRBN) binding moiety acting as serine/threonine-protein kinase Nek7 degradation inducers reported to be useful for the treatment of amyotrophic lateral sclerosis, Still’s disease, Behçet’s disease, familial Mediterranean fever, Alzheimer’s disease, pulmonary arterial hypertension and more.
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Art concept for molecular glue degradation
Cancer

Vaxcellbio advances research in MYO1D-targeted degradation

Nov. 25, 2025
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Vaxcellbio Co. Ltd. has signed a research agreement with the Korea Drug Development Fund (KDDF) to pursue the discovery of next-generation targeted anticancer lead compounds based on degradation of the molecular motor protein MYO1D (myosin 1D).
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Cancer

New PLK1 degradation inducers disclosed in Crossfire Oncology patent

Nov. 21, 2025
Crossfire Oncology BV has divulged proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a serine/threonine-protein kinase PLK1 (STPK13) targeting moiety through a linker reported to be useful for the treatment of cancer, autoimmune diseases, transplant rejection, neurological disorders and inflammatory disorders.
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Cancer

New GSPT1/CSNK1A1 degradation inducers disclosed in Mindrank patent

Nov. 19, 2025
Mindrank Therapeutics (Suzhou) New Drug Research & Development Co. Ltd. has divulged molecular glue degraders comprising cereblon (CRBN) ligands acting as dual eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) and casein kinase 1 isoform α (CSNK1A1) degradation inducers. They are reported to be potentially useful for the treatment of cancer, Alzheimer’s disease, inflammatory disorders, autoimmune diseases and metabolic diseases.
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Breast cancer illustration
Cancer

CDK2 degraders show activity in HR+/HER2- and CCNE1-amplified breast tumors

Nov. 14, 2025
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During the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, scientists from Plexium Inc. presented the identification of a new class of potent, selective, cereblon (CRBN)-based molecular glue degraders of CDK2 using its proprietary monovalent degrader platform.
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Cancer

Shanghai Leadingtac Pharmaceutical divulges new KRAS G12D degradation inducers

Nov. 12, 2025
Shanghai Leadingtac Pharmaceutical Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety covalently linked to a GTPase KRAS (G12D mutant)-targeting moiety via a linker reported to be useful for the treatment of cancer.
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Wooden stamp with China flag
Cancer

Evopoint’s XNW-34017 gains clinical trial clearance in China

Nov. 12, 2025
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Evopoint Biosciences Co. Ltd. has obtained clinical trial clearance in China for XNW-34017, an oral protein degrader that targets Aurora kinase A (AURKA) while simultaneously degrading MYC.
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Concept of business partnership
Drug design, drug delivery & technologies

Evotec and BMS partnership yields IND approval

Nov. 12, 2025
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Evotec SE has received a $5 million milestone payment from Bristol Myers Squibb Co. (BMS), following the acceptance of an IND application by the FDA in the companies’ strategic protein degradation partnership.
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Illustration of lungs with cancer inset
Cancer

TRI-611 targets ALK fusion and TKI-resistant NSCLC

Nov. 11, 2025
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Researchers at Triana Biomedicines Inc. presented the preclinical characterization of TRI-611, a CNS-penetrant molecular glue degrader targeting ALK in models of ALK fusion-positive non-small-cell lung cancer.
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Cardiovascular

Monte Rosa’s MRT-8102 suppresses NLRP3 inflammasome activation

Nov. 11, 2025
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Researchers from Monte Rosa Therapeutics Inc. reported preclinical efficacy data on MRT-8102, a selective NEK7 molecular glue degrader, designed to treat inflammatory diseases.
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