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BioWorld - Saturday, May 30, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Hengrui invests $301M to launch investment firm; achieves positive phase III prostate cancer data

June 14, 2022
By Doris Yu
Jiangsu Hengrui Medicine Co. Ltd., its subsidiary Shengdi Investment Management Holding Co. Ltd., and Hengrui Group are to invest ¥2.01 billion (US$301 million) to jointly set up an equity investment company targeting pharmaceutical and health care companies.
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Boehringer Ingelheim to develop A*STAR antibodies for targeted cancer therapies

June 14, 2022
By David Ho
Singapore’s Agency for Science, Technology and Research (A*STAR) has inked a deal with Boehringer Ingelheim GmbH to develop and commercialize targeted cancer therapies.
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Hamlet and Neurochase partner to develop novel technology to deliver Alpha-1H for CNS tumors

June 14, 2022

NXP-900 shows tumor growth inhibition and survival benefit in mouse model of group 4 medulloblastoma

June 14, 2022

Fochon Pharmaceuticals identifies new BTK inhibitors

June 14, 2022

Qilu Regor Therapeutics presents new STING antagonists

June 14, 2022
Acute myeloid leukemia illustration

Daiichi Sankyo’s quizartinib doubles overall survival in patients with newly diagnosed FLT3-ITD-positive AML

June 13, 2022
By Tamra Sami
Daiichi Sankyo Co. Ltd.’s quizartinib met the primary endpoint of overall survival in the pivotal phase III Quantum-First study, which tested the addition of quizartinib to chemotherapy vs. chemotherapy alone for adults with newly diagnosed FLT3-ITD-positive acute myeloid leukemia (AML).
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Day One’s phase II findings with ‘drug to beat’ may inaugurate new era in pediatric brain cancer

June 13, 2022
By Randy Osborne
Day One Biopharmaceuticals Inc.’s phase II data with tovorafenib from the Firefly-1 study in pediatric brain cancer dazzled Wall Street, and shares (NASDAQ:DAWN) closed $14.96, up $8.34, or 126%.
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Everest wins first approval in China for breast cancer drug Trodelvy

June 13, 2022
By Doris Yu
Everest Medicines Ltd. has picked up its first marketing approval in China for Trodelvy (sacituzumab govitecan), a medicine licensed from Gilead Sciences Inc. It was approved to treat adults with unresectable locally advanced or metastatic triple-negative breast cancer who have received two or more prior systemic therapies, at least one of them for metastatic disease.
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Imcheck closes $84M series C round for gamma-delta T-cell activating antibody

June 13, 2022
By Cormac Sheridan
Imcheck Therapeutics SAS raised €80 million (US $83.5 million) in a series C round to maintain the momentum of its lead development program, ICT-01, an immunostimulatory antibody that activates gamma-delta T cells.
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