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BioWorld - Saturday, May 2, 2026
Home » molecular glue degraders

Articles Tagged with ''molecular glue degraders''

Cancer

Shanghai Meiyue Biotech Development presents new molecular glue degraders

April 24, 2026
Shanghai Meiyue Biotech Development Co. Ltd. has divulged molecular glue degraders comprising an E3 ubiquitin-protein ligase/proto-oncogene Vav (VAV1) interaction inducer and VAV1 degradation inducer. They are designed for potential use in the treatment of cancer, autoimmune diseases, cardiovascular, renal, metabolic, inflammatory and neurological disorders.
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Cancer

HBS1L degradation inducers named in Tango Therapeutics patent

April 20, 2026
Tango Therapeutics Inc. has synthesized substituted piperidine-dione molecular glue degraders comprising E3 ubiquitin ligase-binding moiety and acting as HBS1-like protein (HBS1L; HBS1) degradation inducers for use in the treatment of cancer.
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Gastrointestinal

Hubei Bio-Pharmaceutical Industrial Technological Institute divulges new VAV1 degraders

April 14, 2026
Hubei Bio-Pharmaceutical Industrial Technological Institute Inc. has identified new molecular glue degrader compounds acting as proto-oncogene Vav (VAV1)/protein cereblon (CRBN) interaction inducers for degradation of VAV1 reported to be useful for the treatment of inflammatory bowel disease.
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Handshake, businessmen holding dollar sign, lightbulb
Cancer

Gilead exercises option to license Kymera’s KT-200

April 10, 2026
No Comments
Gilead Sciences Inc. has exercised its option to exclusively license KT-200, a first-in-class, oral CDK2 molecular glue degrader development candidate discovered and characterized by Kymera Therapeutics Inc. under the parties’ strategic collaboration agreement.
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Inflammatory

Qilu Pharma describes new VAV1 degradation inducers

March 24, 2026
Shanghai Qilu Pharmaceutical Research and Development Centre Ltd. has prepared and tested molecular glue degraders comprising E3 ubiquitin-protein ligases acting as proto-oncogene Vav (VAV1) degradation inducers reported to be useful for the treatment of inflammation and autoimmune diseases.
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Immune

Innocare presents new VAV1 degradation inducers

March 19, 2026
Beijing Innocare Pharma Tech Co. Ltd. and Innocare Pharma Inc. have patented molecular glue degraders acting as VAV1 degradation inducers. They are reported to be useful for the treatment of autoimmune disease and inflammatory disorders.
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Immune

VAV1 degradation inducers reported in new Humanwell Healthcare patents

March 11, 2026
Humanwell Healthcare (Group) Co. Ltd. has divulged molecular glue degraders comprising cereblon (CRBN)-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are reported to be useful for the treatment of autoimmune disease, cancer, inflammatory bowel disease, multiple sclerosis, myasthenia gravis, periodontitis, psoriasis, rheumatoid arthritis and type I diabetes, among others.
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Art concept for molecular glue degradation
Immune

Innocare’s VAV1 degrader ICP-538 cleared for clinic in China

Feb. 9, 2026
No Comments
Beijing Innocare Pharma Tech Co. Ltd. has gained IND clearance in China to conduct clinical trials of ICP-538, an orally administered molecular glue degrader targeting VAV1, which is a key protein downstream of T-cell and B-cell receptors. ICP-538 is being studied for the treatment of autoimmune diseases, such as inflammatory bowel disease, systemic lupus erythematosus and multiple sclerosis.
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Hematologic

Linkcure Therapeutics divulges new WIZ degradation inducers

Jan. 12, 2026
Linkcure Therapeutics has synthesized molecular glue degraders acting as zinc finger protein 803 (ZNF803; WIZ) degradation inducers reported to be useful for the treatment of sickle cell anemia and β-thalassemia.
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Cardiovascular illustration

Cardio works out for Monte Rosa in NEK7 phase I

Jan. 7, 2026
By Randy Osborne
No Comments
Monte Rosa Therapeutics Inc. followed up December’s positive prostate cancer data with strong interim findings from a phase I study with MRT-8102, a NEK7-directed molecular glue degrader in the works for inflammatory conditions driven by the NLRP3 inflammasome, IL-1, and IL-6.
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