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BioWorld - Monday, June 22, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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ASH 2019

Identifying and sometimes removing treatment and research barriers

Dec. 9, 2019
By Lee Landenberger
ORLANDO, Fla. – While disparities remain in putting minority and older patients into clinical trials and being treated for blood cancers, there are successes in getting once-ignored patients into the mix so they can receive the same treatments as others. 
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ASH 2019

Genentech showcases new data on CD20-CD3 bispecific for tough-to-treat lymphomas

Dec. 9, 2019
By Michael Fitzhugh
ORLANDO, Fla. - Chimeric antigen receptor T (CAR T) cells have proved to be a major advance in treating patients with refractory B-cell malignancies so far. But, often, in approaching those issues "we solve one and we create another," Stephen Schuster, a doctor at the Abramson Cancer Center at the University of Pennsylvania in Philadelphia, told reporters at the 61st American Society of Hematology (ASH) annual meeting Saturday.
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‘Fergene’ therapy in BCG-stubborn bladder cancer, Instiladrin instills phase III confidence

Dec. 6, 2019
By Randy Osborne
The “remarkably appealing” route of administration and every-three-month dosing put Ferring Pharmaceuticals SA’s nadofaragene firadenovec (rAd-IFN/Syn3, also known as Instiladrin) in strong position for approval in high-grade Bacillus Calmette-Guérin (BCG) unresponsive non-muscle invasive bladder cancer (NMIBC).  
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New PCa treatment strategy may overcome resistance

Dec. 6, 2019
By John Fox
Targeting prostate cancer (PCa) neuroendocrine (NE) cells via inhibition of the C-X-C motif chemokine receptor 2 (CXCR2) is an androgen receptor (AR)-independent therapeutic strategy that can improve the efficacy of treatment for PCa, a leading cause of male cancer mortality.
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Emphasizing synergy and efficiency, EOC Pharma raises $71M series C to fight breast, gastric cancers

Dec. 6, 2019
By Elise Mak
BEIJING – EOC Pharmaceutical Group, of Shanghai, completed a series C financing round, bagging $71 million to advance its lead programs EOC-103 and EOC-315 for breast and gastric cancers. The round was led by Hangzhou Tigermed Consulting Co. Ltd. and its affiliated funds, TF Capital and Yingke PE. Hanne Capital and Everest Venture Capital also participated in the round. In 2017, EOC raised $32 million in a series B round. All funding participants are China-based.
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Cancer-focused Black Diamond raises $85M series C

Dec. 5, 2019
By Michael Fitzhugh
Tumor-agnostic therapy developer Black Diamond Therapeutics Inc. has completed an oversubscribed series C financing of $85 million. The Cambridge, Mass.-based company said proceeds will help it advance candidates targeting oncogenic driver mutations of the ErbB kinases in EGFR and HER2, starting with a combined phase I/II trial of its most advanced candidate next year.
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Rapt licenses FLX-475 to Hanmi in deal worth up to $118M

Dec. 5, 2019
By Jihyun Kim
HONG KONG – Rapt Therapeutics Inc., of San Francisco, and Seoul, South Korea-based Hanmi Pharmaceutical Co. Ltd. entered a license agreement for Rapt’s FLX-475 in Asia. FLX-475 is an oral, small-molecule CCR4 antagonist for cancer treatment. 
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Propelling ahead, Civetta raises a $53M series A

Dec. 4, 2019
By Lee Landenberger
Civetta Therapeutics LLC will take a $53 million series A to advance its platform and programs based on beta-propeller proteins that mediate protein-to-protein interactions. Those proteins can become involved in cancers, neurodegeneration and metabolic disorders, with oncology being the company’s initial focus.
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Imcheck closes $53M B round for antibodies targeting gamma delta T cells

Dec. 4, 2019
By Cormac Sheridan
DUBLIN – Imcheck Therapeutics SAS raised €48 million (US$53.2 million) in a series B financing round to move a pipeline of antibodies targeting gamma delta T cells into the clinic.
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GI Innovation licenses GI-101 to Simcere at maximum $796 million

Dec. 2, 2019
By Jihyun Kim
HONG KONG – Seoul, South Korea-based GI Innovation Inc. has licensed to Nanjing, Jiangsu-based Simcere Pharmaceutical Co. Ltd. rights to its immunotherapy drug candidate, G1-101, a bispecific CD80/interleukin2 (IL-2) variant fusion protein.
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