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BioWorld - Saturday, March 28, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Cancer

Discovery of PHB2-targeted chromanone compounds with activity in models of multiple myeloma

Dec. 27, 2022
Researchers from Kbluebio Inc. and affiliated organizations recently reported the discovery and preclinical evaluation of a novel prohibitin-2 (PHB2) ligand as a potential candidate for the treatment of multiple myeloma (MM).
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3D illustration of B-cell lymphoma
Cancer

First-in-class HAT activator enhances immune checkpoint inhibitors

Dec. 27, 2022
Approximately 20,000 patients diagnosed with non-Hodgkin lymphomas died in 2022 despite current treatments; 30-40% of these cases involved diffuse large B-cell lymphoma (DLBCL). Monoallelic mutations in histone acetyltransferases (HATs) occur in over 39% of germinal center DLBCLs. Activation of intact wild-type alleles offers an opportunity to overcome the mutated allele.
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Colorectal cancer illustration
Cancer

Novel SOC inhibitor suppresses migration and invasion of colorectal cancer cells

Dec. 27, 2022
Researchers from Taipei Medical University presented the discovery of novel store-operated calcium channel (SOC) inhibitors as potential anticancer candidates. Synthesis and optimization of a series of difluorobenzamide derivatives led to the discovery of MPT-0M004 as the lead candidate with promising SOC inhibitory activity. In vitro, both migration and invasion of colorectal cancer cells were significantly suppressed after 48 hours of treatment with MPT-0M004, with the growth inhibitory effect of the compound being similar to that seen for the reference SOC inhibitor.
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Immuno-oncology

Legochem Biosciences and Amgen collaborate to develop next-generation ADCs

Dec. 27, 2022
Legochem Bioscience Inc. (LCB) has entered into a research collaboration and license agreement with Amgen Inc., granting Amgen rights to research, develop and commercialize antibody-drug conjugates (ADCs) directed against up to 5 targets selected by Amgen based on LCB’s proprietary Conjuall ADC technology.
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Cancer

Insitu Biologics and Mayo collaborate to advance drug delivery technology for cancer therapeutics

Dec. 23, 2022
Insitu Biologics Inc. has entered into an agreement with the Mayo Foundation for Medical Education and Research to further develop its prolonged-release drug delivery technology for cancer therapeutics.
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Microscopic image of acute myeloid leukemia (AML) cells.
Immuno-oncology

Affimed authorized by French ANSM to begin phase I study of AFM-28 for AML

Dec. 23, 2022
Affimed NV has received clearance of a clinical trial application (CTA) by the French National Agency for the Safety of Medicines and Health Products (ANSM) for a phase I study of AFM-28 (AFM28-101) in CD123-positive relapsed or refractory acute myeloid leukemia (AML).
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Immuno-oncology

Elpiscience's anti-CD39 x TGF-β bispecific antibody ES-014 cleared for phase I study in solid tumors

Dec. 23, 2022
Elpiscience Biopharmaceuticals Inc. has announced Center of Drug Evaluation (CDE) clearance of its IND application for ES-014 for a phase I study in patients with advanced solid tumors.
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3D representation of tumor
Immuno-oncology

FDA clears IND for NBL-020 for advanced solid tumors

Dec. 23, 2022
The FDA has cleared an IND for a clinical trial in the U.S. of NBL-020, a fully human antibody drug independently developed by CSPC Pharmaceutical Group Ltd.'s subsidiary Novarock Biotherapeutics Ltd., for the treatment of advanced solid tumors.
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Cancer

Chinese researchers describe new PARP-1 inhibitors for cancer

Dec. 23, 2022
Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have identified nitrogen-containing heterocyclic compounds acting as poly(ADP-ribose) polymerase 1 (PARP-1; ARTD1) inhibitors reported to be useful for the treatment of cancer.
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Cancer

Innocure Therapeutics divulges new PROTACs for cancer

Dec. 23, 2022
Innocure Therapeutics Inc. has synthesized piperidinedione derivatives acting as proteolysis targeting chimeric (PROTACs) compounds comprising an E3 ubiquitin ligase cereblon (CRBN) binding moiety covalently linked to hepatocyte growth factor receptor (HGFR; MET; c-MET)-targeting moiety via linker reported to be useful for the treatment of cancer.
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