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BioWorld - Friday, January 2, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Chi-Med gears up for China NDA after surufatinib hits phase III endpoint in NET

Oct. 9, 2019
By David Ho
HONG KONG – Hutchison China Meditech Ltd.'s (Chi-Med) is preparing for the next step after surufatinib achieved its primary endpoint in a phase III SANET-ep study in extra-pancreatic advanced neuroendocrine tumors (NETs) in China.
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South Korea's Bioleaders and Israel's Weizmann found JV to advance p53-targeted R&D

Oct. 9, 2019
By Jihyun Kim
HONG KONG – South Korean biotech Bioleaders Co. Ltd., headquartered in Yong-in city, Gyeonggi-do, and Israel's Weizmann Institute of Science, based in Rehovot, recently founded a joint venture in Israel. With the new entity, they will accelerate the R&D of a Weizmann-developed approach targeting p53, a strong tumor suppressor that has proved difficult to drug.
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Australian government urged to provide immunotherapy access for high-risk melanoma patients

Oct. 2, 2019
By Tamra Sami
PERTH, Australia – Australia is at risk of falling behind the U.S. and Europe in preventing recurrence of melanoma, the Melanoma Institute Australia warns. It is urging the Australian government to undertake a timely review of immunotherapy treatments effective in preventing the spread of melanoma and to fast track listings on the government-subsidized Pharmaceutical Benefits Scheme (PBS).
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Study shows just how far precision target ID has yet to go

Sep. 18, 2019
By Nuala Moran
Ten targeted cancer drugs currently being tested in clinical trials involving 1,000 patients do not reach the targets at which they are aimed, according to recently published research.
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Kahr aiming for I-O combo, testing DSP-107 plus Roche PD-L1 in lung cancer study

Sep. 18, 2019
By David Ho
HONG KONG – In one of the latest combination efforts against cancer, Kahr Medical Ltd. is teaming up with Switzerland's Basel-based Roche Holding AG to study the use of the former's lead program, DSP-10, in combination with the latter's PD-L1-blocking checkpoint inhibitor, Tecentriq (atezolizumab), in patients with advanced non-small-cell lung carcinoma refractory to checkpoint inhibitors.
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Led by U.S. scientists, funded by Chinese, cross-border firm Oncologie eyes both markets

Sep. 11, 2019
By Elise Mak
BEIJING – Despite tensions between the U.S. and China, especially in the tech sector, Oncologie Inc. maintains its plans to pursue drug development in both markets. The clinical-stage startup, led by U.S. scientists and funded with Chinese capital, has stationed itself in both Boston and Shanghai to focus on developing innovative cancer therapies simultaneously in China and the U.S.
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