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BioWorld - Tuesday, January 13, 2026
Home » molecular glue degraders

Articles Tagged with ''molecular glue degraders''

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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Prostate cancer cells

GSPT1 chat favorable as Monte Rosa scores in prostate phase I/II

Dec. 16, 2025
By Randy Osborne
No Comments
Monte Rosa Therapeutics Inc. plans a signal-verifying phase II trial next year after making known the positive interim data from an ongoing phase I/II trial testing molecular glue degrader MRT-2359 in combination with androgen receptor (AR) inhibitor Xtandi (enzalutamide, Astellas Pharma Inc.). The investigation targeted heavily pretreated patients with metastatic castration-resistant prostate cancer bearing AR mutations.
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Gold dollar sign inside gold cog
Cancer

Series B financing supports Triana’s molecular glue degraders

Dec. 4, 2025
No Comments
Triana Biomedicines Inc. has closed an oversubscribed $120 million series B financing round to advance its molecular glue degrader pipeline.
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AI generated, 3D rendering of protein degradation
Cancer

Oral GSPT1 degraders show potent antitumor activity

Dec. 2, 2025
No Comments
G1 to S phase transition 1 (GSPT1) is a protein involved in cell cycle progression, translation termination, and protein homeostasis, and its overexpression has been implicated in various cancers. Although GSPT1 is considered a promising therapeutic target, the lack of conventional ligand-binding pockets has historically rendered it undruggable.
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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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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
No Comments
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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Illustration of lungs with cancer inset
Cancer

TRI-611 targets ALK fusion and TKI-resistant NSCLC

Nov. 11, 2025
No Comments
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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Cancer

Novel selective degrader disclosed for transcription factor IKZF2

Oct. 10, 2025
No Comments
IKZF2, a transcription factor in the Ikaros family, plays a key role in stabilizing regulatory T (Treg) cells and promoting immune suppression within the tumor microenvironment (TME). Selective targeting of IKZF2 in intratumoral Tregs has the potential to enhance antitumor immunity and improve the efficacy of immunotherapy, while minimizing immune-related toxicities associated with systemic Treg depletion.
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