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BioWorld - Wednesday, April 8, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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Polyphor lands $15M up front in back-loaded China deal for balixafortide

Aug. 31, 2020
By Cormac Sheridan
DUBLIN – Shares in Polyphor AG gained as much as 12% during early trading Aug. 31 on news of a deal in China for its lead drug, balixafortide, which is currently undergoing a phase III trial in HER2-negative locally recurrent or metastatic breast cancer.
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Triumvira raises $55M series A to advance new T-cell platform

Aug. 27, 2020
By Michael Fitzhugh
Triumvira Immunologics Inc., a U.S.-Canadian immuno-oncology startup, has raised $55 million in series A financing to back a pipeline of four new T-cell therapy candidates for the potential treatment of both liquid and solid tumors. Bayer AG's Leaps unit and Northpond Ventures led the round. China-based Oceanpine Capital and Viva Biotech Holdings also provided funds.
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Leukemia illustration

Sierra club membership to widen as myelofibrosis Momentum builds?

Aug. 27, 2020
By Randy Osborne
Vancouver, British Columbia-based Sierra Oncology Inc. during its recent earnings call offered an update on momelotinib, in phase III development for myelofibrosis. Enrollment in the study won’t be finished until the fourth quarter of 2021.
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Cancer cell, dropper, test tubes

Kinnate advances early stage cancer programs with $98M series C

Aug. 26, 2020
By Michael Fitzhugh
Kinnate Biopharma Inc., a San Diego-based company focused on the discovery and development of small-molecule kinase inhibitors for genomically defined cancers, has raised $98 million in a series C financing.
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Novartis' anti-PD1 spartalizumab falls short in phase III melanoma trial

Aug. 24, 2020
By Michael Fitzhugh
A phase III study evaluating a combination of a Novartis AG anti-PD-1 candidate with the well-established BRAF/MEK inhibitor combo in first-line unresectable or metastatic BRAF V600 mutant melanoma missed its primary endpoint of progression-free survival.
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Onconova eyes the bench as I.V. rigosertib misses its primary endpoint

Aug. 24, 2020
By Lee Landenberger
Onconova Therapeutics Inc.’s lead candidate in myelodysplastic syndromes took a major hit Monday as the small molecule I.V. rigosertib failed to meet the primary endpoint of significantly improved survival vs. best supportive care in higher-risk patients.
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Tesetaxel broken axle? Odonate’s Contessa barefoot despite phase III endpoint win

Aug. 24, 2020
By Randy Osborne
Adverse events (AEs) took the shine off Odonate Therapeutics Inc.’s long-awaited top-line data from the phase III trial called Contessa testing the oral taxane chemotherapy tesetaxel in metastatic breast cancer (MBC), and shares of the San Diego-based firm (NASDAQ:ODT) closed at $18.33, down $15.21, or 45%.
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‘Closed’ case

Orally active STING agonists stimulate innate immunity

Aug. 20, 2020
By Anette Breindl
Stimulator of interferon genes (STING) is a protein that senses DNA in the cytosol, where it comes from either an infectious invader or a damaged nucleus and sets off an immune response that ultimately results in the activation of T cells. STING agonists are among the strategies that have been tested in hopes they would increase the response rate to checkpoint blockade. Now, back-to-back papers in the Aug. 21, 2020, issue of Science have detailed the preclinical development of orally available STING agonists.
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Innovent out-licenses ex-China rights for PD-1 drug to Lilly in $1.03B deal

Aug. 19, 2020
By Elise Mak
Innovent Biologics Inc., of Suzhou, has out-licensed ex-China rights for its PD-1 drug Tyvyt (sintilimab) to Eli Lilly and Co. in an expanded license deal. The Chinese firm will receive $200 million upfront in the deal, the value of which could approach up to $1.03 billion.
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Jiangsu Hengrui gets Korea’s green light to pursue drug combo in phase III HCC trial

Aug. 18, 2020
By Gina Lee
HONG KONG – China’s Lianyungang-based Jiangsu Hengrui Medicine Co. Ltd. has obtained approval from Korea’s Ministry of Food and Drug Safety (MFDS) to begin a phase III trial for a combination therapy of its PD-1 inhibitor candidate camrelizumab and VEGFR-2 inhibitor rivoceranib.
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