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BioWorld - Friday, March 27, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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Crystalgenomics in good position after signing camrelizumab license agreement

May 6, 2020
By Gina Lee
HONG KONG – After inking a recent deal with China’s Jiangsu Hengrui Medicine Co. Ltd., South Korea’s Crystalgenomics Inc. is celebrating its 20th anniversary by seeking more partners to further develop its anti-PD-1 inhibitor pipeline.
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Leukemia illustration
The umbralisib and ublituximab band

TG Therapeutics sings U2 interim success in CLL

May 5, 2020
By Brian Orelli
TG Therapeutics Inc. got a dose of good news when the independent data safety monitoring board recommended that the UNITY-CLL study be stopped early for superior efficacy after an interim analysis showed its umbralisib and ublituximab combination (U2) helped patients with chronic lymphocytic leukemia (CLL).
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Hand holding "Acquisition" piece over puzzle

Italy’s Menarini Group enters the U.S. cancer market by acquiring Stemline in a deal worth up to $677M

May 4, 2020
By Lee Landenberger
The business of cancer therapy in the U.S. is where the big money is, and the Menarini Group, a privately held Italian pharma and diagnostics company, just got a place at the table with its acquisition deal worth up to $677 million for New York’s Stemline Therapeutics Inc.
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AACR 2020

Phosphatases are yin to kinases’ yang

May 1, 2020
By Anette Breindl
The activity of many proteins is controlled through phosphorylation by kinases and dephosphorylation by phosphatases. Overactive kinases are one of the major drivers of tumors and, as a result, kinase inhibitors are a mainstay of oncology drug development. But “activation of the brakes, the phosphatases, could be equally therapeutically viable for the treatment of a broad range of cancers” to kinase inhibition, Goutham Narla told the audience at the 2020 American Association for Cancer Research (AACR) meeting.
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Hit or miss in mimesis? Albeit early, Neoleukin lookin’ good

April 30, 2020
By Randy Osborne
Seattle-based Neoleukin Therapeutics Inc. is targeting the end of 2020 for an IND submission related to prospective cancer immunotherapy NL-201, described as an engineered, hyperstable agonist of interleukin-2 (IL-2) and IL-15. It’s meant to eliminate alpha receptor binding and thereby overcome the problems with native IL-2.
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Wall Street hails Chimerix viral load; COVID-19, smallpox bids forge onward

April 29, 2020
By Randy Osborne
A pair of good-news items from Chimerix Inc. pushed the Durham, N.C.-based company’s stock (NASDAQ:CMRX) to $2.15, closing up 64 cents, or 42%, higher as backers reacted to near-term NDA plans for smallpox countermeasure brincidofovir (BCV) and the start of a phase II/III trial with dociparstat sodium (DSTAT) in COVID-19 patients with acute lung injury (ALI).
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Despite a phase III stumble, Blueprint forges ahead with avapritinib as Deciphera rallies

April 28, 2020
By Lee Landenberger
The phase III failure of Blueprint Medicines Corp.’s avapritinib to meet its primary endpoint of improving progression-free survival (PFS) in patients with locally advanced unresectable or metastatic gastrointestinal stromal tumors (GIST) pummeled the company stock on Tuesday but boosted shares and hopes at Deciphera Pharmaceuticals Inc.
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Cancer cell, dropper, test tubes
AACR 2020

New drugs on the horizon highlighted at AACR

April 28, 2020
By Brian Orelli
CYBERSPACE – At a series of new drugs on the horizon sessions at the 2020 American Association for Cancer Research (AACR) Virtual Annual Meeting I, a variety of companies presented preclinical and clinical data for promising early stage oncology products.
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Adam Buchanan, Geisinger Genomic Medicine Institute
AACR 2020

First prospective peek at Thrive’s Cancerseek reveals gaps in liquid biopsy testing

April 28, 2020
By Cormac Sheridan
DUBLIN – Thrive Earlier Detection Corp. and its academic and clinical collaborators have provided a first glimpse at the utility of a liquid biopsy test as a screening tool for picking up cancers in an asymptomatic population. In an interim one-year readout of data from the prospective five-year DETECT-A study in 10,000 women, an early version of Thrive’s Cancerseek test picked up 26 cancers ahead of standard-of-care screening, while the latter modality picked up another 24 cancers that Cancerseek missed.
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Antibodies
1+1=5

After a slow start, bispecific antibody space takes off

April 27, 2020
By Brian Orelli
Blincyto (blinatumomab, Amgen Inc.), the first FDA-approved bispecific antibody, gained regulatory approval in 2014, but the intervening years have been fairly bleak for bispecific antibodies as companies worked through technical challenges.
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