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BioWorld - Friday, February 27, 2026
Home » Topics » Degradation inducer, BioWorld Science

Degradation inducer, BioWorld Science
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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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Cancer

Pan-KRAS degradation inducers disclosed in Shanghai Leadingtac Pharmaceutical patent

Nov. 10, 2025
Shanghai Leadingtac Pharmaceutical Co. Ltd. has divulged proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety covalently linked to a pan-KRAS-targeting moiety through a linker.
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Cancer

Simcere Pharmaceutical divulges new STAT6 degradation inducers

Nov. 7, 2025
Simcere Pharmaceutical Co. Ltd. has synthesized proteolysis targeting chimeras (PROTACs) comprising E3 ubiquitin-protein ligands coupled to a signal transducer and activator of transcription 6 (STAT6)-targeting moiety via a linker reported to be useful for the treatment of cancer and inflammatory disorders.
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Cancer

MT-4561 exerts antitumor efficacy in NUT carcinoma

Nov. 7, 2025
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NUT carcinoma is a rare and aggressive cancer tied to the BRD4-NUT fusion protein, with poor prognosis and lack of effective therapy.
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Cancer

Accutar presents development of PI3Kα degrader-antibody conjugates

Nov. 6, 2025
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Accutar Biotechnology Inc. recently presented preclinical data on AC-4847, a first-in-class PI3Kα-targeting degrader-antibody conjugate (DAC) designed for selective treatment of PI3Kα-driven cancers.
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Hands holding holographic intestine
Gastrointestinal

Eilean presents in vivo data on MALT1 degrader TE-205

Nov. 6, 2025
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Eilean Therapeutics LLC has presented in vivo data for its first-in-class MALT1 degrader, TE-205, as a disease-modifying therapy for ulcerative colitis.
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