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BioWorld - Wednesday, February 11, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Shanghai Zheye Biotechnology patents G12C mutant GTPase KRAS inhibitors

Sep. 23, 2021
Woman using Paige software on tablet

Paige receives FDA de novo authorization for AI product for prostate cancer detection

Sep. 22, 2021
By Annette Boyle
The FDA granted de novo marketing authorization for Paige Prostate, artificial intelligence (AI)-driven software that improves detection of prostate cancer. The clinical study submitted to the FDA demonstrated that using Paige Prostate resulted in a 7% improvement in sensitivity in correctly diagnosing cancer, increasing from 89.5% to 96.8%.
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Conference data for Sept. 22, 2021: ESMO

Sep. 22, 2021
New and updated preclinical and clinical data presented by biopharma firms at the European Society for Medical Oncology Congress 2021, including: Aprea, Redx, Syros.
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Conference data for Sept. 21, 2021: ESMO

Sep. 22, 2021
New and updated preclinical and clinical data presented by biopharma firms at the European Society for Medical Oncology Congress 2021, including: Astellas, Astrazeneca, Beyondspring, Byondis, Carsgen, Cstone, Daiichi, Exelixis, Genentech, Genmab, GT, Innovent, Immunocore, Ipsen, Janssen, Merck, Mirati, Novartis, Ose, Regeneron, Sanofi, Spectrum, Verastem, Veru.
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Theragnostics and AAA to jointly develop Ga-68 one-step PET radiopharmaceuticals

Sep. 22, 2021

Discovery of novel BRAF dimer inhibitors with promising efficacy

Sep. 22, 2021

Fochon Pharmaceuticals describes CDK2/CDK4/CDK6 inhibitors

Sep. 22, 2021

Beyondspring NSCLC phase III hits primary endpoint but stock sags anyway

Sep. 21, 2021
By Lee Landenberger
Despite Beyondspring Pharmaceuticals Inc.’s phase III study meeting its primary and key secondary endpoints of a plinabulin/docetaxel combination in treating non-small-cell lung cancer (NSCLC), the company stock (NADAQ:BYSI) took a pounding. Shares sunk 32.9% on Sept. 20 to close at $15.36 each.
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FDA Approved stamp with pills

FDA approves Takeda’s Exkivity for rare form of lung cancer

Sep. 21, 2021
By Richard Staines
Takeda Pharmaceutical Co. Ltd. has grabbed a slice of the non-small-cell lung cancer (NSCLC) market, becoming the first company to gain FDA approval for an oral drug targeted against a rare form of the disease.
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FDA accepts Beigene’s first filing outside China; BLA seeks nod for anti-PD-1 tislelizumab

Sep. 21, 2021
By Doris Yu
The FDA has accepted for review Novartis AG and Beigene Ltd.’s BLA filing for the anti-PD-1 monoclonal antibody tislelizumab.
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