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BioWorld - Wednesday, April 1, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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Wall Street sign

All eyes (virtually) focused on ASCO: Which companies will impress Wall Street?

May 28, 2020
By Peter Winter
The American Society of Clinical Oncology (ASCO) annual meeting will be closely watched by analysts and investors alike. There is no doubt that favorable data presented at the event will advance a company's stock valuation significantly. Equally, candidate cancer therapies that do not live up to expectations will see their developers face the ire of investors.
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CAR T cell attacking cancer cells

Edigene, Immunochina betting on allogeneic CAR T therapy in cancer collaboration

May 28, 2020
By Elise Mak
SUZHOU, China – Genome editing startup Edigene Inc. and CAR T developer Immunochina Pharmaceuticals Co. Ltd., both from Beijing, have unveiled joint efforts to develop an allogeneic CAR T therapy for cancer. Terms remain undisclosed.
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Hands holding gears

Gold, plated: Arcus covenant with Gilead commands potential $2B chestful

May 27, 2020
By Randy Osborne
Arcus Biosciences Inc. “brings the milk without [Gilead Sciences Inc.] having to buy the whole cow” is the way one analyst characterized the pair’s 10-year cancer immunotherapy deal, which could be worth as much as $2 billion, and some may have detected downside for Arcus, as shares (NYSE:RCUS) closed May 27 at $27.05, down $6.49, or 19%. Foster City, Calif.-based Gilead is paying Arcus, of Hayward, Calif., $175 million up front, shelling out a $200 million equity investment, and pledging potentially $1.6 billion or more in the form of R&D support, opt-in cash and milestone payments.
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Steven Yatomi-Clarke, CEO, Prescient Therapeutics

Australia’s Prescient Therapeutics develops next-gen CAR T therapies with UPenn universal immune receptor

May 27, 2020
By Tamra Sami
PERTH, Australia – Melbourne-based Prescient Therapeutics Pty Ltd. is poised to develop next-generation CAR T therapies after signing an exclusive global licensing deal with the University of Pennsylvania for a universal immune receptor technology platform.
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Immune cell density plot
Reversal of ApoE4tune

Germline ApoE variants affect melanoma trajectory

May 26, 2020
By Anette Breindl
Variants in the APOE gene are the strongest genetic risk factor for developing Alzheimer’s disease (AD). Now, researchers at Rockefeller University have demonstrated that APOE variants also affected the risk of progression and metastasis as well as the response to immunotherapy, in melanoma.
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SK Group prepares IPO for subsidiary SK Biopharmaceuticals

May 26, 2020
By Gina Lee
HONG KONG – South Korean conglomerate SK Group is preparing to list its subsidiary, SK Biopharmaceuticals Co. Ltd., on the Stock Market Division of the Korea Exchange.
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IPO line graph

Kintor’s $240M IPO well received in Hong Kong; CEO says internal early stage R&D will be future focus

May 22, 2020
By Elise Mak
BEIJING – Androgen receptor (AR)-related disease specialist Kintor Pharmaceutical Ltd., of Suzhou, China, raised $240 million on the Hong Kong Stock Exchange (HKEX) on May 22 by issuing 92.3 million shares at HK$20.15 apiece. The IPO was oversubscribed by 551 times, showing the city’s biotech fever.
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China’s Carsgen set to start trials for first claudin18.2-targeted CAR T-cell therapy

May 21, 2020
By Elise Mak
BEIJING – CAR T-cell therapeutics developer Carsgen Therapeutics Co. Ltd., of Shanghai, won IND clearance from the FDA for its first-in-class CT-041 for advanced gastric and pancreatic cancers. The company said it is the first claudin18.2 (CLDN18.2)-targeted CAR T-cell therapy cleared for clinical trials in the world.
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FDA Approved stamp with pills

FDA's approval of Lynparza for mCPRC shades Rubraca win

May 20, 2020
By Michael Fitzhugh
Just days after Clovis Oncology Inc.'s Rubraca (rucaparib) became the first PARP inhibitor approved by the FDA to treat certain cases of metastatic prostate cancer (mCPRC) in third-line care, the agency granted an even broader label in the indication to its first-in-class competitor, Lynparza (olaparib). Endorsement of second-line use of Lynparza in mCPRC and an overall survival (OS) benefit listed in its updated label will help rapidly establish it as "the drug of choice in the [second] line, leaving little commercial opportunities for Rubraca downstream," SVB Leerink analyst Andrew Berens said.
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Hands holding arrow-shaped puzzle pieces

Zentalis Pharmaceuticals receives $20 million series A financing to set up Chinese JV

May 20, 2020
By David Ho
HONG KONG – New York and San Diego-based Zentalis Pharmaceuticals Inc. has gained $20 million in a series A financing round to support a Chinese joint venture called Zentera Therapeutics.
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