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BioWorld - Tuesday, January 6, 2026
Home » Keywords » mantle cell lymphoma

Items Tagged with 'mantle cell lymphoma'

ARTICLES

Microscope with laptop displaying histology image.
Cancer

Oral cyclin D1-selective inhibitors with antitumor activity, improved safety profile

Nov. 19, 2025
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At the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, researchers from Circle Pharma Inc. presented their recent work on developing novel compounds that specifically target cyclin D1 while avoiding the toxicity associated with targeting cyclin D3.
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Cancer

Shanghai Helioson Pharmaceutical describes new BTK degradation inducers

Sep. 1, 2025
Shanghai Helioson Pharmaceutical Co. Ltd. has identified proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin-protein ligase-binding moiety covalently bonded to a Bruton tyrosine kinase (BTK)-targeting moiety through a linker. They are reported to be useful for the treatment of cancer and autoimmune diseases.
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Mantle cell lymphoma
Cancer

[161Tb]Tb-BL34L20S, new radiotracer targeting CXCR4 for cancer

July 8, 2025
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A team of researchers at the University of British Columbia investigated the potential of radiopharmaceutical therapy based on Terbium-161 (161Tb) both in vitro and in vivo using a novel tracer, [161Tb]Tb-BL34L20S, which uses the C-X-C chemokine receptor type 4 (CXCR4)-targeting peptide BL34L20S labeled to 161Tb.
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Cancer

Biopolar Hongye (Nantong) Pharmaceutical discovers new BTK degradation inducers

Dec. 23, 2024
Biopolar Hongye (Nantong) Pharmaceutical Co., Ltd. has described proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin ligase cereblon (CRBN) binding moiety covalently linked to a Bruton’s tyrosine kinase (BTK) binding moiety reported to be useful for the treatment of cancer, inflammatory and autoimmune diseases.
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Cancer

Baylor College of Medicine patents new BTK, IKZF1 and IKZF3 degradation inducers

Dec. 13, 2024
Baylor College of Medicine has disclosed proteolysis targeting chimeras (PROTACs) comprising cereblon (CRBN) ligands coupled to Bruton tyrosine kinase (BTK)-, DNA-binding protein Ikaros (IKZF1)- and Zinc finger protein Aiolos (IKZF3)-targeting moieties through a linker.
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Cancer

Jiangsu Vcare Pharmatech discovers new BTK degradation inducers

Sep. 5, 2024
Jiangsu Vcare Pharmatech Co. Ltd. has described proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a Bruton’s tyrosine kinase (BTK) targeting moiety via a linker reported to be useful for the treatment of cancer.
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Clinical trial virtual display
Immuno-oncology

Verismo’s Synkir-310 receives FDA clearance for phase I trial in NHL

May 15, 2024
Verismo Therapeutics Inc. has received IND clearance from the FDA to conduct a phase I trial with Synkir-310 for non-Hodgkin lymphoma (NHL).
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Immuno-oncology

Zeno Management describes new ROR1-targeting ADCs for cancer

Feb. 26, 2024
Zeno Management Inc. has identified antibody-drug conjugates comprising antibodies targeting inactive tyrosine-protein kinase transmembrane receptor ROR1 (ROR1) covalently bound to exatecan derivatives through a linker.
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CAR T cells attacking cancer cell
Immuno-oncology

Elicera’s CAR T-cell therapy ELC-301 cleared to enter clinic in Sweden for B-cell lymphoma

Feb. 12, 2024
Elicera Therapeutics AB has received approval from the Swedish Medical Products Agency to start a phase I/II study of chimeric antibody receptor (CAR) T-cell therapy ELC-301 in patients with refractory or relapsed B-cell lymphoma.
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Cancer

Shanghai Institute of Materia Medica divulges new CRBN/target protein interaction inducers

Jan. 18, 2024
Shanghai Institute of Materia Medica of the Chinese Academy of Sciences has synthesized molecular glue compounds targeting protein cereblon (CRBN) acting as CRBN/target protein interaction inducers reported to be useful for the treatment of cancer.
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More Articles Tagged with 'mantle cell lymphoma'

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