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BioWorld - Thursday, January 1, 2026
Home » Topics » Asia-Pacific » China

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Impact and Burning Rock team up to develop companion diagnostics for synthetic lethality drugs

Aug. 10, 2021
By David Ho
Burning Rock Biotech Ltd. has formed a global strategic partnership with Impact Therapeutics Inc. to develop companion diagnostics for a pipeline of drugs in the field of synthetic lethality.
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Grit Bio closes series A+ round to develop the first TIL therapy in China

Aug. 10, 2021
By Doris Yu
Cell therapy company Zhuhai Grit Biotechnology Inc. completed a series A+ financing of undisclosed value to advance its lead tumor-infiltrating lymphocyte (TIL) program, GT-101 for advanced solid tumors, into the clinic by year end while also developing other TIL candidates in its pipeline.
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Coronavac product packaging

Sinovac reports positive data on COVID-19 booster, loss of antibodies within months

Aug. 10, 2021
By Sergio Held
Sinovac Biotech Ltd. said booster shots of its Coronavac vaccine against SARS-CoV-2 induce strong immune responses in adult and elderly populations following a considerable loss of antibodies six to eight months after completing the current two-dose regimen.
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Yen-Yuan currency symbol

Grit Bio closes series A+ round to develop the first TIL therapy in China

Aug. 9, 2021
By Doris Yu
Cell therapy company Zhuhai Grit Biotechnology Inc. completed a series A+ financing of undisclosed value to advance its lead tumor-infiltrating lymphocyte (TIL) program, GT-101 for advanced solid tumors, into the clinic by year end while also developing other TIL candidates in its pipeline.
Read More
Atrial fibrillation illustration

Microport raises $150M in series C for CRM business

Aug. 6, 2021
By David Ho
Microport Scientific Corp.’s cardiac rhythm disorders subsidiary, Microport Cardiac Rhythm Management Ltd. (Microport CRM), has confirmed agreements for a series C financing that would net it total investment proceeds of $150 million. Hillhouse Capital Group and Microport will co-lead the series C investment with investments of $20 million and $47 million, respectively.
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Akeso’s PD-1 drug wins China approval for Hodgkin’s lymphoma

Aug. 6, 2021
By Elise Mak
Akeso Inc. became the fifth company to score an approval for a homegrown PD-1 antibody in China, with penpulimab cleared for relapsed or refractory (r/r) classic Hodgkin’s lymphoma (cHL). The company is seeking more approvals for nasopharyngeal and lung cancers in both China and the U.S. to stand out in the increasingly competitive PD-1 space.
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SARS-CoV-2 illustration turns from blue to red

Chinese vaccines move one step closer to preventing Delta variant COVID-19

Aug. 5, 2021
By Doris Yu
Preliminary real-world data showed that Chinese inactivated vaccines are 63% protective against the COVID-19 Delta variant, China’s top epidemiologist Zhong Nanshan said at the 24th Respiratory Disease Academic Conference of Guangdong Medical Association in Guangzhou.
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Map of China

Impact and Burning Rock team up to develop companion diagnostics for synthetic lethality drugs

Aug. 5, 2021
By David Ho
Burning Rock Biotech Ltd. has formed a global strategic partnership with Impact Therapeutics Inc. to develop companion diagnostics for a pipeline of drugs in the field of synthetic lethality.
Read More

Vaccine firm Gdk Biotechnology debuts on Shanghai Star Market with $187M IPO

Aug. 3, 2021
By Doris Yu
Jiangsu Gdk Biotechnology Co. Ltd. will further develop its vaccine pipeline after it started trading on the Shanghai Stock Exchange Star Market on Aug. 2, where it raised ¥1.21 billion ($187 million) through an initial public offering of 22 million shares. The company plans to use the proceeds from the listing to establish a manufacturing plant to produce its quadrivalent influenza vaccine and invest in R&D for other vaccine candidates, as well as replenish working capital and repay bank loans.
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Chinese flag and pills

Chinese regulator releases new guideline to evaluate clinical value of drugs

Aug. 3, 2021
By Doris Yu
China’s National Health Commission has just released a new set of regulations to evaluate the clinical value of both approved drugs and those still in trials as part of its efforts to improve the market standards.
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