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BioWorld - Wednesday, December 24, 2025
Home » Topics » Drugs » Degradation inducer

Degradation inducer
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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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Cancer

Shanghai Apeiron Biotechnology patents new PRMT5 degradation inducers

Nov. 5, 2025
Shanghai Apeiron Biotechnology Co. Ltd. has disclosed proteolysis targeting chimeras (PROTACs) reported to be useful for the treatment of cancer.
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Immune

Hengrui scientists patent new TYK2 inhibitors and/or degradation inducers

Nov. 4, 2025
Jiangsu Hengrui Pharmaceuticals Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have disclosed non-receptor tyrosine-protein kinase TYK2 inhibitors and/or degradation inducers reported to be useful for the treatment of psoriasis, cancer, rheumatoid arthritis, asthma and more.
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AI generated, 3D rendering of protein degradation
Cancer

Tango’s first-in-class HBS1L/PELO degrader for FOCAD-deleted cancers

Oct. 31, 2025
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Loss of FOCAD in cells impairs normal mRNA surveillance, creating a dependency on the HBS1L/PELO complex for ribosome rescue and identifying HBS1L as a potential synthetic lethal target and therapeutic vulnerability.
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Cancer cells under magnifying glass
Cancer

Foghorn Therapeutics shares progress on three protein degrader programs

Oct. 31, 2025
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Foghorn Therapeutics Inc. has presented details on its protein degrader programs selectively targeting ARID1B, CBP and EP300.
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Cancer

Haisco Pharmaceutical divulges new PROTACs targeting EGFR

Oct. 30, 2025
Haisco Pharmaceutical Group Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to an EGFR (HER1; erbB1)-targeting moiety through a linker.
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Cancer

New TEAD1 degradation inducers disclosed in Amphista patent

Oct. 27, 2025
Amphista Therapeutics Ltd. has divulged proteolysis targeting chimera (PROTAC) compounds comprising an F-Box only protein 22 (FBXO22)-binding moiety coupled to a transcriptional enhancer factor TEF (TEAD)-targeting moiety through a linker reported to be useful for the treatment of cancer.
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Cancer

Aurigene Oncology describes new SMARCA2 and SMARCA4 degradation inducers

Oct. 15, 2025
Aurigene Oncology Ltd. has identified proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase protein binding moiety covalently linked to probable global transcription activator SNF2L2 (SMARCA2; BAF190B; SNF2-α) and/or transcription activator BRG1 (SMARCA4; BAF190A; SNF2-β) binding moieties through a linker reported to be useful for the treatment of cancer.
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Cancer

Kelun-Biotech divulges new GTPase KRAS G12D mutant degradation inducers

Oct. 14, 2025
Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising a Von Hippel-Lindau disease tumor suppressor (VHL)-binding moiety covalently linked to a GTPase KRAS G12D mutant-targeting moiety through a linker reported to be useful for the treatment of cancer.
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