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BioWorld - Thursday, April 16, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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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 Elise Mak and David Ho
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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South Korean won

Bionetix secures $9.33M in series B funding for AML/MDS and glaucoma treatment

Jan. 21, 2020
By Jihyun Kim
HONG KONG – Bionetix Inc., of Suwon, South Korea, has secured ₩10.8 billion (US$9.33 million) in series B funding. The biotech, founded in February 2017, has attracted a total of KRW14.7 billion to date. The company will use the funds to advance NTX-301, a therapy for myelodysplastic syndrome/acute myeloid leukemia (MDS/AML) with epigenetic dysregulation, and NTX-101, a glaucoma treatment.
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Aum Biosciences partners with Cyclica for cancer therapies development

Jan. 21, 2020
By Jihyun Kim and Elise Mak
HONG KONG - Singapore-based biotech Aum Biosciences Pte. Ltd., and Toronto, Canada-based biotech Cyclica Inc. have agreed to work together to apply Cyclica’s drug discovery platform in Aum’s R&D programs for the discovery of potential new cancer therapies. Aum will deploy its drug R&D skills including a biomarker-driven approach while Cyclica will contribute its AI-augmented platforms, Ligand Design and Ligand Express.
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IPO, coins, financial chart

China’s I-Mab goes public in targeted range for $103.7M; after-market deep Zai?

Jan. 21, 2020
By Randy Osborne
Shanghai-based I-Mab Biopharma Co. Ltd. became the first IPO out of the gate this year, pricing its IPO of about 7.4 million American depositary shares (ADSs) – each 10 representing 23 ordinary shares of the company, par value $0.0001 per share – at $14 each, within the planned range of $12 at the low end and $15 at the high. But the stock’s performance might not have been all investors hoped, as shares (NASDAQ:IMAB) closed at $12.50 Jan. 17.
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Chi-Med’s surufatinib phase III trial halted early after meeting primary endpoint in advanced pancreatic NET

Jan. 21, 2020
By Elise Mak
BEIJING – Hong Kong-headquartered Hutchison China Meditech Ltd.’s (Chi-Med) called an early stop to its phase III pivotal study of surufatinib in advanced pancreatic neuroendocrine tumors (NET) in China after it met the predefined primary endpoint of progression-free survival.
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