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BioWorld - Wednesday, December 10, 2025
Home » Topics » Asia-Pacific » China

China
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Opportunity compass with Chinese flag

Foreign pharma’s strategy for China: Lower price for a bigger pie

Dec. 27, 2019
By Elise Mak
BEIJING – China is aggressively pushing its goal to make drugs more affordable, and foreign pharma giants are adjusting their pricing strategy for a market that comprises nearly 20% of the world’s population and is expected to continue growing.  
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U.S.-China capsule

Tracon buys rights to subcutaneous PD-L1 antibody from China’s 3D Medicines and Alphamab

Dec. 24, 2019
By Elise Mak
BEIJING – U.S. biotech Tracon Pharmaceuticals Inc., of San Diego, has in-licensed from Chinese drugmakers 3D Medicines (Beijing) Co. Ltd. and Jiangsu Alphamab Biopharmaceuticals Co. Ltd. the rights to develop envafolimab, a subcutaneous PD-L1 antibody, to treat soft tissue sarcoma in North America.
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Stem cells

China approves two more CAR T trials; Legend’s candidate gets FDA breakthrough status

Dec. 24, 2019
By Elise Mak
BEIJING – China made strides in the CAR T space this month. The country approved two more candidates to enter clinical trials in December, and forerunner Nanjing Legend Biotech Co. Ltd. said its investigational CAR T therapy LCAR-B38M/JNJ-4528 co-developed with Janssen Biotech Inc. won FDA’s breakthrough therapy designation.
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Lungs

Scientists report insights into the mechanics, literally, of IPF

Dec. 20, 2019
By John Fox
A Chinese study has established a previously unknown direct mechanistic link between elevated mechanical tension caused by impaired alveolar regeneration and progressive idiopathic pulmonary fibrosis (IPF), highlighting a pathogenic mechanism that may underlie fibrosis.
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China approves two more CAR T trials; Legend’s candidate gets FDA breakthrough status

Dec. 20, 2019
By Elise Mak
BEIJING – China made strides in the CAR T space this month. The country approved two more candidates to enter clinical trials in December, and forerunner Nanjing Legend Biotech Co. Ltd. said its investigational CAR T therapy LCAR-B38M/JNJ-4528 co-developed with Janssen Biotech Inc. won FDA’s breakthrough therapy designation.
Read More

Hui-Gene closes $14M series A to advance safe gene editing for rare diseases

Dec. 18, 2019
By Elise Mak
BEIJING – Gene therapy startup Hui-Gene Therapeutics Ltd. Co., of Shanghai, said it secured more than ¥100 million (US$14 million) in a series A financing round to develop a safer gene therapy to treat genetic diseases caused by single-base mutations.
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Approved stamp

Qilu scores first Avastin biosimilar approval in China, set to drive down prices

Dec. 17, 2019
By Elise Mak
BEIJING – Jinan, China-based Qilu Pharmaceutical Co. Ltd. has won the first approval for a China-developed biosimilar to Avastin (bevacizumab, Roche Holding AG). Its biosimilar QL-1101, to be sold under the trade name Ankada, has been approved to treat advanced, metastatic or recurrent non-small-cell lung cancer and metastatic colorectal cancer.
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Chinese investors launch new AU$45M fund to develop South Australian biotech

Dec. 17, 2019
By Tamra Sami
PERTH, Australia – Private Chinese investors have launched a new AU$45 million (US$31.17 million) investment fund to accelerate the development and commercialization of new biotechnology from South Australia for the global market.
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Globe showing China

First ever comprehensive blood disease research platform to be built for China

Dec. 16, 2019
By David Ho
HONG KONG – Boston-based consulting firm Analysis Group Inc. will be working with China’s Institute of Hematology & Blood Diseases Hospital (IHBDH) on developing a first-of-its-kind blood disease research platform. The National Longitudinal Cohort of Hematological Diseases in China (NICHE) is set to hold the information of more than 10,000 patients across China.
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Approved stamp

Qilu scores first Avastin biosimilar approval in China, set to drive down prices

Dec. 16, 2019
By Elise Mak
BEIJING – Jinan, China-based Qilu Pharmaceutical Co. Ltd. has won the first approval for a China-developed biosimilar to Avastin (bevacizumab, Roche Holding AG). Its biosimilar QL-1101, to be sold under the trade name Ankada, has been approved to treat advanced, metastatic or recurrent non-small-cell lung cancer and metastatic colorectal cancer.
Read More
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