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BioWorld - Sunday, July 5, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Conference data for Nov. 8, 2022: SITC

Nov. 8, 2022
New and updated preclinical and clinical data presented by biopharma firms at the Society for Immunotherapy of Cancer Annual Meeting including: Affimed, Compugen, Genenta, Geneos, Hummingbird, Iovance, Nextcure, Nouscom, Oncolytics.
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Cancer

Mirati Therapeutics discovers new KRAS G12C inhibitors for NSCLC

Nov. 8, 2022
Mirati Therapeutics Inc. has described GTPase KRAS (G12C mutant) inhibitors reported to be useful for the treatment of cancer, in particular non-small-cell lung cancer (NSCLC).
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Cancer

The Cleveland Clinic Foundation patents CIT inhibitors with utility for medulloblastoma and prostate cancer

Nov. 8, 2022
The Cleveland Clinic Foundation has disclosed citron rho-interacting kinase (CRIK; CIT) inhibitors reported to be useful for the treatment of medulloblastoma and prostate cancer.
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Cancer

Navrogen enters CRADA with NCI to study anti-mesothelin ADC NAV-001 in clinic

Nov. 8, 2022
Navrogen Inc. has entered into a cooperative research and development agreement (CRADA) with researchers at the U.S. National Cancer Institute (NCI), part of the National Institutes of Health (NIH). Under this CRADA, Navrogen will sponsor the clinical investigation of the experimental antibody-drug conjugate (ADC) NAV-001, under supervision of the NCI.
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Concept art for cells receptors, inhibitors
Cancer

TYRA-200 retains potency across multiple resistance mutations

Nov. 8, 2022
Inhibition of emerging polyclonal on-target acquired resistance mutations remains a critical unmet need in the treatment of fibroblast growth factor receptor 2 (FGFR2)-driven tumors. In the current study, researchers from Tyra Biosciences Inc. presented the preclinical characterization of a novel FGFR1/2/3 inhibitor, TYRA-200, being developed for the treatment of cancer.
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Immuno-oncology

Hapten-peptide neoantigens allow selective killing of cancer cells by engineered antibodies

Nov. 8, 2022
Targeted therapies and immunotherapies have revolutionized cancer treatment in recent years. However, achieving durable responses and, ultimately, curing metastatic cancers driven by intracellular oncogenes remains a primary unmet medical need. Although fragments of intracellular oncoproteins can act as neoantigens presented by the major histocompatibility complex (MHC), recognizing the typically minimal differences between oncoproteins and their normal counterparts makes this approach quite challenging.
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Magnetic bacteria
Drug Design, Drug Delivery & Technologies

Magnetic attraction makes bacteria better drug delivery vehicles

Nov. 7, 2022
By Nuala Moran
A new method for controlling naturally magnetized bacteria has improved the prospects of applying them as vehicles for intratumoral delivery of cancer drugs and in hyperthermia therapy. The advance will provide a better way of directing the movement of systemically administered bacteria, using external magnetic fields to target them to tumors sited deep in the body. It also points to a possible route for engineering existing bacteria-based anticancer constructs for better targeting.
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Biocytogen out-licenses CD40 antibody to Isu Abxis to develop trispecific antibodies

Nov. 7, 2022
By Doris Yu
Biocytogen Pharmaceuticals Co. Ltd.’s subsidiary Eucure Biopharma Co. Ltd. has granted Isu Abxis Co. Ltd. rights to use its humanized agonistic anti-CD40 antibody YH-003 to develop cancer drugs.
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Telix’s imaging agent meets primary, secondary endpoints in phase III kidney cancer trial

Nov. 7, 2022
By Tamra Sami
Radiopharmaceutical company Telix Pharmaceuticals Ltd’s TLX250-CDx (Zirconium (89Zr) TX250) met both primary and secondary endpoints in the phase III Zircon study in clear cell renal cell carcinoma, according to top-line data.
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GSK blockbuster hopeful Blenrep in trouble as multiple myeloma trial misses target

Nov. 7, 2022
By Richard Staines

There are doubts about the future of GSK plc’s multiple myeloma drug Blenrep (belantamab mafodotin) after it failed to meet its goal of improving progression-free survival compared with standard chemotherapy in a confirmatory trial, placing its conditional approvals in the U.S. and Europe at risk.


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