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BioWorld - Saturday, August 1, 2026
Home » Topics » Asia-Pacific » China

China
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Henlius-Sermonix deal

Sermonix out-licenses China rights of breast cancer drug to Henlius

Jan. 16, 2024
By Marian (YoonJee) Chu
U.S. biopharma Sermonix Pharmaceuticals Inc. handed off China rights of lasofoxifene, an oral endocrine therapy in development for breast cancer, to Shanghai’s Henlius Biotech Inc., for an undisclosed up-front payment and up to $58 million in milestone fees.
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China’s Ji Xing signs flurry of Asian deals to advance cardiovascular pipeline and global ambitions

Jan. 16, 2024
By Tamra Sami
Shanghai-based Ji Xing Pharmaceuticals has signed a number of licensing deals over the last week for China rights to cardiovascular drugs to advance its pipeline and its global ambitions, partnering most recently with Tokyo-based TMS Co. Ltd. after the Chinese company acquired global rights for TMS-007 (also known as BIIB-131) from Biogen Inc.
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Henlius-Sermonix deal

Sermonix out-licenses China rights of breast cancer drug to Henlius

Jan. 12, 2024
By Marian (YoonJee) Chu
U.S. biopharma Sermonix Pharmaceuticals Inc. handed off China rights of lasofoxifene, an oral endocrine therapy in development for breast cancer, to Shanghai’s Henlius Biotech Inc., for an undisclosed up-front payment and up to $58 million in milestone fees.
Read More

China’s Ji Xing signs flurry of Asian deals to advance cardiovascular pipeline and global ambitions

Jan. 12, 2024
By Tamra Sami
Shanghai-based Ji Xing Pharmaceuticals has signed a number of licensing deals over the last week for China rights to cardiovascular drugs to advance its pipeline and its global ambitions, partnering most recently with Tokyo-based TMS Co. Ltd. after the Chinese company acquired global rights for TMS-007 (also known as BIIB-131) from Biogen Inc.
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First PFA device granted NMPA approval in China

Jan. 12, 2024
By Pankhil Paresh and Zsuzsa Lindenmaier
Sichuan Jinjiang Electronic Medical Device Technology Co. Ltd. received approval from China’s National Medical Products Administration (NMPA) approval for the commercial use of its PFA technology in the treatment of atrial fibrillation, making it the first pulsed field ablation device to gain approval in the country.
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China’s NMPA accepts Hutchmed’s sovleplenib NDA for primary immune thrombocytopenia

Jan. 11, 2024
By Tamra Sami
China’s National Medical Products Administration (NMPA) has accepted for review Hutchmed’s NDA for sovleplenib (HMPL-523) for treatment of primary immune thrombocytopenia.
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Richard Lee, CEO, Lotte Biologics, at JPM24

Asia CDMO giants Wuxi and Samsung to grow production, ADC capacity

Jan. 10, 2024
By Marian (YoonJee) Chu
Major contract research development and manufacturing organizations (CDMO) out of Asia are announcing plans to ramp up production and antibody-drug conjugate (ADC) capabilities worldwide.
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Back pain
Neurology/Psychiatric

Fermion’s FZ-008-145 for pain relief cleared to enter clinic in China

Jan. 10, 2024
Guangzhou Fermion Technology Co. Ltd. has announced IND clearance by China’s National Medical Products Administration (NMPA) for FZ-008-145 to treat pain.
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Praxis rallies on $279M China deal for tremor drug, pipeline updates

Jan. 9, 2024
By Marian (YoonJee) Chu
Boston-based Praxis Precision Medicines Inc.’s shares rose nearly 25% on Jan. 8 after it announced a pipeline update and licensing deal for its tremor drug, ulixacaltamide (PRAX-944), with Shanghai’s Tenacia Biotechnology Co. Ltd.
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Man measuring waist

Innovent’s mazdutide meets endpoints in phase III obesity trial

Jan. 9, 2024
By Tamra Sami
Innovent Biologics Inc. said its glucagon-like peptide-1 receptor and glucagon receptor dual agonist, mazdutide, met the primary endpoints and all key secondary endpoints in its first phase III trial in Chinese adults who were overweight or obese. The company plans to submit the first mazdutide NDA for weight management to China's NMPA shortly.
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