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BioWorld - Sunday, December 21, 2025
Home » Topics » Asia-Pacific » China

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HTA and drug/device pricing in Asia in 2020

Dec. 31, 2019
By David Ho
MALAYSIA – Asian countries, like India, have been struggling to find a middle ground to the effective pricing of drugs and medical devices over the past year and several are looking at health technology assessment (HTA) programs as a solution for this issue in the coming year.
Read More
Gavel and block with Chinese flag

Chinese scientist faces three years in jail for creating world’s first gene-edited babies

Dec. 31, 2019
By Nuala Moran and Elise Mak
BEIJING – Chinese scientist He Jiankui has been sentenced to three years in prison and fined ¥3 million (US$429,421) for illegally carrying out the human embryo gene editing that led to the birth of twin girls and another baby with heritable changes to their genomes.  
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Opportunity compass with Chinese flag

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

Dec. 31, 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. To achieve its goals, China is using its huge population, which stands at 1.43 billion, as a bargaining chip to negotiate prices with pharmaceutical companies.
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HTA and drug/device pricing in Asia in 2020

Dec. 31, 2019
By David Ho
MALAYSIA – Asian countries, like India, have been struggling to find a middle ground to the effective pricing of drugs and medical devices over the past year and several are looking at health technology assessment (HTA) programs as a solution for this issue.
Read More
Gavel and block with Chinese flag

Chinese scientist faces three years in jail for creating world’s first gene-edited babies

Dec. 30, 2019
By Elise Mak and Nuala Moran
BEIJING – Chinese scientist He Jiankui has been sentenced to three years in prison and fined ¥3 million (US$429,421) for illegally carrying out the human embryo gene editing that led to the birth of twin girls and another baby with heritable changes to their genomes.  
Read More
2019-2020 blocks

Year in Review: From capital markets to CRISPR, 2019 a pretty good year for biopharma

Dec. 30, 2019
For biopharma, 2019 can be described as a terrific year – with a few asterisks. The financial markets were flourishing, with venture capital dollars, in particular, flowing to the sector, while dealmaking reached historic proportions. Meanwhile, scientific breakthroughs led the way as cell and gene therapies gained ground, the first signs of success emerged with new technologies like CRISPR and the long-awaited promise of genomics found its way to the front lines of health care.
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Health professional holding tablet, medical icons

HTA and drug/device pricing in Asia in 2020

Dec. 27, 2019
By David Ho
MALAYSIA – Asian countries, like India, have been struggling to find a middle ground to the effective pricing of drugs and medical devices over the past year and several are looking at health technology assessment (HTA) programs as a solution for this issue in the coming year. Boston-headquartered consulting firm Analysis Group Inc. recently looked at how HTA programs in Japan, South Korea and China varied and what could be gleaned from their experiences.
Read More
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.  
Read More
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.
Read More
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