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BioWorld - Monday, January 12, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Person holding stomach in pain

Taiho picks up nod for Jeselhy to treat gastrointestinal stromal tumors in Japan

June 28, 2022
By Doris Yu
Japan’s Ministry of Health, Labour and Welfare has given Otsuka Holdings Co. Ltd. subsidiary Taiho Pharmaceutical Co. Ltd. the green light for its oral heat shock protein 90 (HSP90) inhibitor Jeselhy (pimitespib) to treat gastrointestinal stromal tumors (GIST) that have progressed after chemotherapy. The company will soon commercialize the drug in Japan.
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Antibody-drug conjugate illustration

Sutro to develop immunostimulatory ADCs for Astellas targets in deal worth $1.3B

June 28, 2022
By Tamra Sami
Astellas Pharma Inc. and Sutro Biopharma Inc. signed an exclusive global licensing deal under which Sutro will develop immunostimulatory antibody-drug conjugates (iADCs) for three biological targets for Astellas.
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Antibody-drug conjugate
Newco news

Profoundbio completes $70M series A round to advance ADC programs to the clinic

June 14, 2022
By Tamra Sami
Profoundbio Inc. closed a $70 million series A financing round that will see it advance its two lead antibody-drug conjugate (ADC) programs to the clinic. The Suzhou, China, and Woodinville, Wash.-based company has raised a total of more than $138 million in the past two years.
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Acute myeloid leukemia illustration

Daiichi Sankyo’s quizartinib doubles overall survival in patients with newly diagnosed FLT3-ITD-positive AML

June 14, 2022
By Tamra Sami
Daiichi Sankyo Co. Ltd.’s quizartinib met the primary endpoint of overall survival in the pivotal phase III Quantum-First study, which tested the addition of quizartinib to chemotherapy vs. chemotherapy alone for adults with newly diagnosed FLT3-ITD-positive acute myeloid leukemia (AML).
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China in red on globe

Everest wins first approval in China for breast cancer drug Trodelvy

June 14, 2022
By Doris Yu
Everest Medicines Ltd. has picked up its first marketing approval in China for Trodelvy (sacituzumab govitecan), a medicine licensed from Gilead Sciences Inc. It was approved to treat adults with unresectable locally advanced or metastatic triple-negative breast cancer who have received two or more prior systemic therapies, at least one of them for metastatic disease.
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Hengrui invests $301M to launch investment firm; achieves positive phase III prostate cancer data

June 14, 2022
By Doris Yu
Jiangsu Hengrui Medicine Co. Ltd., its subsidiary Shengdi Investment Management Holding Co. Ltd., and Hengrui Group are to invest ¥2.01 billion (US$301 million) to jointly set up an equity investment company targeting pharmaceutical and health care companies.
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Boehringer Ingelheim to develop A*STAR antibodies for targeted cancer therapies

June 14, 2022
By David Ho
Singapore’s Agency for Science, Technology and Research (A*STAR) has inked a deal with Boehringer Ingelheim GmbH to develop and commercialize targeted cancer therapies.
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Lung cancer data help move the market as ASCO 2022 begins

June 7, 2022
By Lee Landenberger
The world’s biggest cancer-focused conference began June 3 as more than 40,000 attendees are expected at the American Society of Clinical Oncology’s (ASCO) annual gathering. The conference is being held in live in Chicago and is also available virtually. Among the more than 2,500 abstract presentations in about 120 subject subcategories are potential breakthroughs in treating non-small-cell lung cancer from Immutep Ltd., Cullinan Oncology Inc. and Surface Oncology Inc. Each company has seen upticks in their stock value, some as much as 10%, during the week as the conference approached and their data are presented.
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Enhertu.png

Swing low, sweet Enhertu: Astrazeneca, Daiichi ASCO data carry HER2 message home

June 7, 2022
By Randy Osborne
The “showdown” at the American Society of Clinical Oncology (ASCO) meeting foreseen by one analyst between breast cancer drugs from Gilead Sciences Inc. and Astrazeneca plc with partner Daiichi Sankyo Co. Ltd. didn’t quite materialize.
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Lung cancer illustration

Henlius’ PD-1 drug shows positive data in phase III trial to treat ES-SCLC

June 7, 2022
By Doris Yu
Shanghai Henlius Biotech Inc.’s anti-PD-1 monoclonal antibody serplulimab has generated positive data in a phase III trial as a first-line treatment for extensive-stage small-cell lung cancer (ES-SCLC).
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