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BioWorld - Sunday, May 10, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Lisa Park, CEO, Prestige Biopharma

Prestige Biopharma aims to become leading cancer drug developer

July 25, 2023
By Marian (YoonJee) Chu
Prestige Biopharma Ltd. is mounting efforts to rise rank through the industry with a two-pronged strategy of becoming a global cancer antibody drug developer and contract development and manufacturing organization.
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China approves Daiichi Sankyo/Astrazeneca’s Enhertu for HER2 low metastatic breast cancer

July 18, 2023
By Tamra Sami
China’s NMPA approved Daiichi Sankyo Co. Ltd. and Astrazeneca plc’s Enhertu (fam-trastuzumab deruxtecan) as the first HER2-directed therapy for patients with HER2-low metastatic breast cancer.
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Genequantum, Aimedbio partner again to develop five more ADCs

July 18, 2023
By Marian (YoonJee) Chu
Another collaboration between two biopharmaceutical companies in the Asia-Pacific region is adding fuel to an already heated fire for antibody-drug conjugate (ADC) development worldwide. Suzhou, China-headquartered Genequantum Healthcare Co. Ltd. and South Korea’s Aimedbio Inc. recently announced extending an existing partnership to jointly develop five ADC investigative drugs.
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Two arrows in opposite directions

TIGIT in troubled waters as Novartis, Beigene end $1B deal for ociperlimab

July 18, 2023
By Marian (YoonJee) Chu
From Roche Holding AG to Novartis AG, bad news abounds for anti-TIGIT immunotherapies. In an SEC filing on July 11, Chinese oncology R&D firm Beigene Ltd. and Basel, Switzerland-based Novartis announced an end to their $1 billion deal to develop the former’s TIGIT immunotherapy ociperlimab, with the checkpoint inhibitor going back to Beigene.
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HLB's Elevar subsidiary confirms FDA to review rivoceranib by 2024

July 18, 2023
By Marian (YoonJee) Chu
Elevar Therapeutics Inc. said that the U.S. FDA accepted its NDA for oral tyrosine kinase inhibitor rivoceranib in combination with PD-1 inhibitor camrelizumab (Airuika) as a first-line treatment for liver cancer. The FDA stamped an official PDUFA target action date of May 16, 2024.
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Genequantum strikes deal for its ADC conjugation technology with Inxmed

July 18, 2023
By Tamra Sami
On the heels of a licensing deal last week, Genequantum Healthcare Co. Ltd. has struck another deal, this time out-licensing its conjugation technology to Inxmed Co. Ltd. to support development of next-generation targeted antibody-drug conjugates (ADCs).
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Jacobio’s KRAS G12C inhibitor progresses to pivotal trials in China for pancreatic cancer

July 11, 2023
By Tamra Sami
China’s Center for Drug Evaluation has cleared Jacobio Pharmaceuticals Group Co. Ltd.’s KRAS G12C inhibitor, glecirasib (JAB-21822), to begin a phase III pivotal study for pancreatic cancer.
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Antibody
Newco news

Haemalogix’s Kappamab hits endpoints in phase IIb myeloma trial

July 11, 2023
By Tamra Sami
Haemalogix Ltd.’s monoclonal antibody Kappamab met all primary endpoints in a phase IIb trial that combined the MAb with lenalidomide and dexamethasone in kappa-type multiple myeloma patients who had relapsed or become refractory to other treatments.
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Building CDMO reach, Lotte Biologics partners with Kanaph for ADC-tech platform

July 11, 2023
By Marian (YoonJee) Chu
Lotte Biologics Co. Ltd. said it partnered with domestic bioventure Kanaph Therapeutics Inc. to develop an antibody-drug conjugate (ADC) technology platform in hopes of rounding out a full, in-house ADC value-chain.
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Kelun-Biotech raises $174M in Hong Kong IPO to race in ADC market

July 11, 2023
Kelun-Biotech Biopharmaceutical Co. Ltd. raised HK$1.36 billion (US$174 million) in an IPO in Hong Kong to support its push into the increasingly competitive antibody-drug conjugate (ADC) market in China.
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