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BioWorld - Friday, April 24, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Cancer

Parenchyma Biotech presents new AhR agonists

Oct. 27, 2022
Parenchyma Biotech Inc. has described aryl hydrocarbon receptor (AhR) agonists reported to be useful for the treatment of cancer and autoimmune disease.
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Cancer

Kansai Medical University discovers new compounds for cancer treatment

Oct. 27, 2022
Kansai Medical University has identified compounds reported to be useful for the treatment of cancer.
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Cancer

French researchers disclose new antibody-drug conjugates for cancer

Oct. 27, 2022
Mablink Bioscience SAS., Université Claude Bernard Lyon 1 and Centre National de la Recherche Scientifique have patented antibody-drug conjugates consisting of antibodies covalently linked to therapeutic drugs through an enzyme-triggered self-immolative linker reported to be useful for the treatment of cancer.
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Drug R&D concept image.
Cancer

ASP-3082, a PROTAC that selectively degrades KRAS G12D protein, shows potent in vivo antitumor efficacy

Oct. 27, 2022
Kirsten rat sarcoma viral oncogene (KRAS) is one of the GTPases from the RAS family activating signaling pathways that regulate cell functions. KRAS mutation of glycine to aspartate at position 12 (G12D) is a common mutation in pancreatic ductal adenocarcinoma, colorectal cancer, lung adenocarcinoma and other solid tumors. ASP-3082 is a proteolysis targeting chimera (PROTAC) under development by Astellas Pharma Inc. The company has presented the first in vitro and in vivo results of this new compound.
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Pancreatic cancer cells.
Cancer

TTX-MC138 shows efficacy in preclinical model of pancreatic adenocarcinoma

Oct. 27, 2022
Transcode Therapeutics Inc. has reported positive preclinical results with its lead candidate, TTX-MC138, which targets microRNA-10b (miR-10b). The company evaluated the bioactivity of TTX-MC138 monotherapy in a murine model of pancreatic adenocarcinoma.
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Brain cancer illustration
Immuno-oncology

FDA approves orphan drug application for TLR-AD1 immunotherapy

Oct. 27, 2022
Novaccess Global Inc. has announced the approval of its application with the FDA for orphan drug designation for TLR-AD1, a vaccine immunotherapy for the treatment of aggressive brain cancers, including glioblastoma and other high-grade gliomas. The company’s therapeutic path involves a unique transformational process, which involves the addition of proprietary substances to create a cocktail for more personalized treatment that substantially increases clinical benefits for patients.
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Cancer

Novel ocotillol derivative shows efficacy in preclinical models of P-gp-mediated MDR

Oct. 27, 2022
P-glycoprotein (P-gp) is a multidrug resistance (MDR)-associated protein, which is widely distributed in membranes of several cells including hepatocytes, renal proximal tubular cells and brain capillary endothelial cells. The overexpression of this drug efflux transporter protein is considered to play a key role in the development of MDR.
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The Combat of Rama and Ravana.
Cancer

ENA 2022: Mutant specific or target selective, that is the question for drug development

Oct. 27, 2022
By Mar de Miguel and Anette Breindl
Diwali, the Festival of Light, marks different events depending on where it is celebrated. In some areas of India, it marks the return of Lord Rama to his birthplace of Ayodhya after defeating the demon Ravana. For Vivek Subbiah, associate professor at the Department of Investigational Cancer Therapeutics, Division of Cancer Medicine of the MD Anderson Cancer Center, the story of how Rama defeated Ravana has parallels in drug discovery. Ravana had 10 heads, and when one was cut off, it grew back. Rama defeated Ravana by means of a magic arrow that entered through the demon’s navel.
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Real fluorescence microscopic view of human neuroblastoma cells

Y-mabs’ Omblastys gets chilly reception in ODAC briefing docs

Oct. 26, 2022
By Randy Osborne
Briefing documents related to the Oct. 28 meeting of the Oncologic Drugs Advisory Committee (ODAC) to deliberate over Y-mabs Therapeutics Inc.’s Omblastys (131I-omburtamab) took aim at the company’s ongoing, pivotal experiment called Study 101, data from which the company highlighted in early October.
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FDA Approved stamp

Janssen’s teclistamab becomes first FDA-approved BCMA bispecific for MM

Oct. 26, 2022
By Jennifer Boggs
The U.S. FDA cleared teclistamab from Janssen Pharmaceutical Cos. as the first bispecific antibody for treating patients with relapsed or refractory multiple myeloma (MM), joining other BCMA-targeted drugs, including an antibody-drug conjugate and CAR T therapies.
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