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BioWorld - Monday, February 16, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Conference data for Sept. 17, 2021: ESMO

Sep. 17, 2021
New and updated preclinical and clinical data presented by biopharma firms at the European Society for Medical Oncology Congress 2021, including: Acepodia, Aileron, Allarity, Amgen, Athenex, Ayala, Bayer, Beyondspring, Bioxcel, Carrick, Exelixis, Gilead, Instil, Laekna, Leap, Macrogenics, Medigene, Medivir, NGM, Nouscom, Oncologie, Psioxus, Second Genome, Shasqi, Silverback, Targovax, Transgene, Zymeworks.
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KRAS protein

KRAS just wants to help: Pancreatic KRAS mutations may be protection gone bad

Sep. 17, 2021
By Anette Breindl
Investigators at MD Anderson Cancer Center have published data suggesting that activating KRAS mutations may be selected for in pancreatitis, because they protect pancreatic tissue from damage.
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Tarveda and SciClone enter license agreement for preclinical PI3K miniature drug conjugates

Sep. 17, 2021

Bantam completes seed funding to advance BTM-3566 toward the clinic

Sep. 17, 2021

Endeavor BioMedicines licenses rights to ULK1/2 inhibitor for LKB1- and RAS-mutated cancers

Sep. 17, 2021

UCL Business describes new CRP inhibitors

Sep. 17, 2021

Bahcesehir Universitesi presents Hdm2 inhibitors

Sep. 17, 2021

KRAS just wants to help: Pancreatic KRAS mutations may be protection gone bad

Sep. 17, 2021
Cancer cell

ESMO 2021: Silverback’s data send stock downward

Sep. 16, 2021
By Lee Landenberger
The European Society for Medical Oncology Congress 2021 has begun with a mix of education and multidisciplinary sessions in addition to symposia. Silverback Therapeutics Inc. was a presenter and took a hit on the market Sept. 16 with its interim phase I/Ib study results showing SBT-6050’s proof of mechanism was established with activated myeloid and T/natural killer cells when treating advanced or metastatic HER2-expressing solid tumors.
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FDA accepts Beigene’s first filing outside China; BLA seeks nod for anti-PD-1 tislelizumab

Sep. 16, 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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