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BioWorld - Sunday, January 4, 2026
Home » Beigene Co. Ltd.

Articles Tagged with ''Beigene Co. Ltd.''

Immuno-oncology

Beigene acquires option to license ADC from Dualitybio for solid tumors

July 11, 2023
Beigene Co. Ltd. and Duality Biologics (Suzhou) Co. Ltd. have signed an agreement for Beigene to acquire an exclusive option for a global clinical and commercial license to a preclinical antibody-drug conjugate (ADC) therapy for select solid tumors.
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3D illustration of B-cell lymphoma
Cancer

BGB-16673 shows a long-term antitumor response in BTK-expressing cancer models

June 15, 2023
Bruton tyrosine kinase (BTK) is involved in cell proliferation and survival in B-cell malignancies. Both covalent and noncovalent BTK inhibitors are in place, but their clinical benefit may be limited due to acquired BTK mutations.
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Biocom-1-pic.png

Biocom 2023: Pharma’s wants and needs in the new market environment

March 2, 2023
By Brian Orelli
During two different panels at Biocom California’s Global Life Science Partnering & Investor Conference, executives from a variety of pharmaceutical companies laid out their wants and needs in the current market environment. Large drug companies have relied on biotech companies to build out their pipelines for many years, but the level of outside inventions has been increasing over the last few years.
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Cancer

Beigene divulges new DGKA and/or DGKZ inhibitors

Feb. 28, 2023
Beigene Co. Ltd. has patented pyrazolopyridinones acting as diacylglycerol...
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Cancer

Beigene presents new MAP4K1 degradation inducers for cancer

Feb. 21, 2023
Beigene Co. Ltd. has divulged proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin ligase binding moiety covalently linked to a mitogen-activated protein kinase kinase kinase kinase 1 (MAP4K1; HPK1; MEKKK1)-targeting moiety reported to be useful for the treatment of cancer.
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Cancer

Beigene divulges new EGFR mutant-targeting PROTACs for cancer

Nov. 25, 2022
Beigene Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN) E3 ubiquitin ligase-binding moiety covalently linked to an EGFR (mutant)-targeting moiety via linker.
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