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BioWorld - Friday, February 27, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Harbour Biomed closes $102.8M series C to advance late-stage programs

July 14, 2020
By Elise Mak
BEIJING – Known for its transgenic mouse platforms to develop antibodies, U.S., China and the Netherlands-based Harbour Biomed Therapeutics Ltd. closed a series C funding round July 9 to raise $102.8 million to advance its late-stage clinical programs and COVID-19 pipeline.
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Immunotech press conference

Immunotech plans to raise $142M on HKEX to advance AAL therapy for liver cancer

June 30, 2020
By Elise Mak
BEIJING – Beijing-based cellular immunotherapy firm Immunotech Biopharm Ltd. said June 28 that it intends to raise up to HK$1.1 billion (US$141.9 million) on the Hong Kong Stock Exchange (HKEX) on July 10, with shares priced between HK$10.5 and HK$11 apiece.
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Ascentage co-develops Bcl-2 and BTK combination therapy for SLL/CLL with Astrazeneca

June 23, 2020
By Elise Mak
BEIJING – Suzhou, China-based Ascentage Pharma Group Inc. said on June 22 that it is working with Astrazeneca plc’s hematology R&D unit, Acerta Pharma, to develop a combination therapy of its Bcl-2 inhibitor, APG-2575, with Acerta's BTK inhibitor, Calquence (acalabrutinib). The first patient has been dosed in the U.S.
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Business, data, dollars illustration

China’s CAR T developer JW Therapeutics closes $100M series B to advance CD19-targeted candidate

June 16, 2020
By Elise Mak
BEIJING – CAR T therapy developer JW Therapeutics (Shanghai) Co. Ltd. raised another $100 million this week after securing $90 million in series A round in 2018. The funds will continue to go toward its lead program, JWCAR-029, a CAR T-cell product targeting CD19 that is now in a phase II study.
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Junshi Biosciences strikes deal with Merck, advances Lilly COVID-19 collaboration

June 9, 2020
By David Ho
HONG KONG – China’s Shanghai Junshi Biosciences Co. Ltd. has struck a deal with Merck KGaA for a clinical trial program in China to investigate the efficacy and safety of Junshi’s anti-PD-1 monoclonal antibody (MAb), Tuoyi (toripalimab) in combination with Merck’s Erbitux (cetuximab) as a treatment for recurrent and/or metastatic squamous cell carcinomas of the head and neck (SCCHN).
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Beigene’s FDA-cleared BTK inhibitor Brukinsa approved in China

June 9, 2020
By Elise Mak
Chinese biotech firm Beigene Ltd. said its second-generation BTK inhibitor, Brukinsa (zanubrutinib), has won approval in China for two indications, entering a market dominated by Imbruvica (ibrutinib, Johnson & Johnson/Abbvie Inc.). The NDA approval came eight months after Brukinsa’s clearance in the U.S.
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Cancer cell

Chi-Med and Beigene partner up to test candidates in combination therapy

June 9, 2020
By David Ho
HONG KONG – Two Chinese biotech companies, Hutchison China Meditech Ltd. (Chi-Med) and Beigene Ltd., are teaming up to evaluate their therapies as combination treatments for several cancers and in different key markets.
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Hand holding gear, dollar sign

Asia-focused Everest Medicines closes $310M series C financing round

June 9, 2020
By Elise Mak
BEIJING – Three-year-old Asia-focused startup Everest Medicines Ltd. closed one of the biggest financing rounds in China’s health care market this year, adding $310 million to its war chest. The firm is aiming to advance its late-stage assets in-licensed from global partners to the China market soon.
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Handshake with globe background and digital overlay

Innovent partners with Roche in multibillion-dollar deal targeting bispecifics, cell therapies

June 9, 2020
By Elise Mak
BEIJING – Suzhou, China-based Innovent Biologics Inc. is known in China as one of the first drugmakers to launch a PD-1 monoclonal antibody. Now, the company is moving to expand its product portfolio and enhance efforts in developing bispecific antibodies and cell therapies in a potential multibillion-dollar deal with pharma giant Roche Holding AG.
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ASCO20: Enhertu improves overall survival in metastatic gastric cancer

June 2, 2020
By Lee Landenberger
The juggernaut that is Daiichi Sankyo Co. Ltd.’s Enhertu continued to roll into this weekend’s American Society of Clinical Oncology virtual meeting, bringing momentum from its December FDA approval for HER2-positive breast cancer, along with fresh data from three new studies in other indications.
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