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BioWorld - Thursday, July 16, 2026
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Home » Topics » BioWorld Asia, China

BioWorld Asia, China
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Prostate cancer cells

Jemincare out-licenses prostate cancer drug to Genentech in $650M deal

Aug. 23, 2022
By Doris Yu
A subsidiary of Jiangxi Jemincare Group Co. Ltd. has out-licensed global rights to its androgen receptor degrader JMKX-002992 to Roche Holding AG and its subsidiary Genentech Inc. in a deal worth up to $650 million.
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Canwell raises ¥100M in series A+ financing for antitumor immunotherapies

Aug. 16, 2022
By Zhang Mengying
Canwell Biotech Ltd. raised more than ¥100 million (US$14.8 million) in a series A+ financing. The funds will help accelerate trials for its pipeline of anticancer assets, such as the TLR7 agonist CAN-1012, and preclinical development of other projects too, CEO Henry Yu told BioWorld. The State Development and Investment Corporation Venture Capital Co. Ltd. was the round’s sole investor.
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Domestic data privacy policies reap global unintended consequences

Aug. 16, 2022
By Mari Serebrov
As biopharma and med-tech companies grapple with restrictive data privacy laws in the EU and China while trying to meet the demand for greater diversity reflective of the U.S. population, there’s been more of an interest in conducting clinical trials in the U.S., Stacy Amin, a partner at Morrison & Foerster LLP, told BioWorld.
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Dollar sign in lightbulb

Glubio nets $22M in series A+ round for targeted protein degradation drugs

Aug. 16, 2022
By Doris Yu
Glubio Therapeutics Inc. has raised $22 million in a series A+ round to support the development of its targeted protein degradation drugs. With the investment, Glubio expects to file INDs for two molecular glue degraders for hematological malignancies in early 2023 in both China and the U.S.
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DNA and cancer cells

Beigene’s tislelizumab hits survival endpoint in phase III HCC study

Aug. 16, 2022
By David Ho
Beigene Ltd.’s tislelizumab met its primary endpoint of noninferior overall survival vs. sorafenib as a first-line treatment in hepatocellular carcinoma (HCC), marking the eighth positive phase III trial readout for the anti-PD-1 drug across multiple cancer types and lines of therapy.
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Gavel and block with Chinese flag

Protecting IP in China still an iffy proposition

Aug. 16, 2022
By Mari Serebrov
Despite new laws and enforcement efforts, protecting intellectual property (IP) rights in China remains a big challenge for companies based in the U.S. and other countries. A case in point is China’s new patent law that came into effect in June 2021.
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Businesswoman pressing dollar sign on touchscreen

Structure Therapeutics nets $33M in financing for GPCR candidates

Aug. 9, 2022
By Doris Yu
Structure Therapeutics Inc. raised $33 million in a financing round to speed up clinical trials of its lead assets targeting chronic diseases and to improve its technology platform. Previously known as Shouti Inc., the company also has rebranded itself as Structure to “reflect its foundation in structural biology and computational design.”
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Cell research illustration

Oricell nets $120M in series B round for cell therapies

Aug. 9, 2022
By Doris Yu
Oricell Therapeutics Co. Ltd. has raised $120 million in a series B financing to support development of its cell therapy pipeline and technology platform, as well as the construction of a manufacturing plant. The round was jointly led by Qiming Venture Partners and Quan Capital Management LLC.
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Gold dollar sign

Sironax raises $200M in series B for RIPK1 inhibitors

Aug. 9, 2022
By David Ho
Sironax Ltd. has raised $200 million in a series B financing round to support the development of its receptor-interacting serine/threonine-protein kinase 1 (RIPK1) inhibitors. The latest financing has brought the capital raised by the Beijing and Shanghai-based company to more than $300 million to date.
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Hutchmed planning regulatory submissions on fruquintinib CRC data

Aug. 9, 2022
By David Ho
It’s an august August for Hutchmed Ltd. as it reported positive business results and a number of trial developments, including results from its pivotal global phase III FRESCO-2 trial evaluating the investigational use of fruquintinib in patients with advanced, refractory metastatic colorectal cancer, which met its primary endpoint of overall survival.
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