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BioWorld - Thursday, May 7, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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Newco news

Standardized delivery of unique neoantigens improves T-cell vaccines

Jan. 24, 2020
By Anette Breindl
When they work, T cells work great. And the folks at Avidea Technologies Inc. want to make them work more often. Combining expertise in immunology and polymer chemistry, the Baltimore-based startup is developing antigen delivery technology to improve T cell-targeted vaccines.
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FDA Approved stamp

Tazemeto, stat: Accelerated win for Epizyme in ES could ‘reFLect’ well in bigger indication

Jan. 24, 2020
By Randy Osborne
Matthew Ros, chief strategy and business officer for Epizyme Inc., said the company is “not providing specific guidance at the moment” about the sales force that will be deployed to market Tazverik (tazemetostat) in follicular lymphoma (FL), an indication for which U.S. regulators are considering the oral, first-in-class EZH2 inhibitor. “But I can assure you we’ve planned very thoughtfully” about the effort, he said. “That's always been a part of why we thought epithelioid sarcoma [ES] was such a strategically important component of the overall business strategy to get on-the-ground experience.” The sales force numbers 19 for now.
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Soon-Shiong’s Nantkwest, Immunitybio still chasing cancer breakthroughs

Jan. 23, 2020
By Michael Fitzhugh
Physician, scientist and investor Patrick Soon-Shiong might be considered a "square peg in a round hole," he admits. But the Abraxane inventor's work to enlist natural killer, dendritic and T cells in what he calls a "triangle offense" against cancer is finally coalescing, he recently told BioWorld.
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Cancer cell and DNA
Precision Medicine World Conference

Cancer genomic tests often aren’t done to guideline; germline data presents unique issues

Jan. 23, 2020
By Stacy Lawrence
SANTA CLARA, Calif. – Just as it does with treatments, the National Comprehensive Cancer Network (NCCN) offers detailed guidelines on genomic testing by cancer type. These are key in determining what physicians can prescribe routinely and what insurers will cover. But those guidelines aren’t followed regularly outside a major research hospital setting, thereby obviating access to tumor genetic information that could help to better guide treatment. Even if current guidelines are followed, physicians and patients can get information back from the tests that neither party is prepared to process.
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Euro money

Ionctura closes series A for next-generation dual-targeting cancer therapies

Jan. 23, 2020
By Nuala Moran
LONDON – Ionctura SA has closed a €15 million (US$16.6 million) series A to fund phase I development of its lead cancer program, IOA-244, and prepare a second product, IOA-289, for clinical development.
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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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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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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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IPO, coins, financial chart

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

Jan. 17, 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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South Korean won

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

Jan. 17, 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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