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BioWorld - Tuesday, June 30, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Incyte identifies PI3Kgamma inhibitors

Jan. 23, 2020

Kinnate Biopharma describes CDK inhibitors

Jan. 23, 2020

Biogen presents new MAP3K5 inhibitors

Jan. 23, 2020

Phase IIb trial approved to evaluate SUBA-Itraconazole in prostate cancer

Jan. 23, 2020

Could SBRT with Cyberknife become new standard of care for recurrent prostate cancer?

Jan. 22, 2020
By Annette Boyle
Nearly 70% of men with locally recurrent prostate cancer who received radiation therapy initially could delay androgen deprivation therapy (ADT) for at least five years following stereotactic body radiation therapy (SBRT) with Accuray Inc.’s Cyberknife system, according to a study published in the International Journal of Radiation Oncology • Biology • Physics.
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PDC*Line Pharma pulls in $22M in equity, grants for lung cancer immunotherapy

Jan. 22, 2020
By Cormac Sheridan
PDC*Line Pharma SA raised €13.9 million (US$15.4 million) in a series B round plus another €6.1 million in loans and grants from the Walloon region of Belgium to take its allogeneic cell-based cancer immunotherapy, PDC*lung-01, into a phase I/II trial in patients with metastatic lung cancer.
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TMPRSS11B as a new therapeutic target in NSCLC

Jan. 22, 2020

African Americans' lung tumors have unstable genomes

Jan. 22, 2020

Miracogen expands ADC deal with Synaffix

Jan. 21, 2020
By David Ho and Elise Mak
HONG KONG – In less than a year, China-based Shanghai Miracogen Inc. has extended its partnership with Oss, the Netherlands based Synaffix BV for a second antibody-drug conjugate (ADCs) candidate. The new deal is similar to one signed last year in that it gives Miracogen nonexclusive rights to Synaffix’s Glycoconnect and Hydraspace ADC technologies for use in a second clinical candidate.
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Oncologie boosts pipeline with phase II-ready bispecific candidate in Mereo deal

Jan. 21, 2020
By Elise Mak
BEIJING – In a deal that adds another clinical-stage program to its pipeline, U.S.-China biotech Oncologie Inc. has picked up global rights to phase II-ready anti-DLL4/VEGF bispecific antibody navicixizumab from London-based Mereo Biopharma Group plc.
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