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BioWorld - Sunday, January 18, 2026
Home » Topics » Asia-Pacific » China

China
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Cowin Biotech nets $156M in Shanghai IPO

Oct. 25, 2022
By Doris Yu
Jiangsu Cowin Biotech Co. Ltd. has raised ¥1.14 billion (US$156 million) in a listing on the Shanghai STAR Market. Its shares opened at ¥42.96 apiece, plunged over 13% by the middle of the day but closed at ¥43.62 on the first trading day on Oct. 25.
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Zelgen’s donafenib garners positive phase III data in differentiated thyroid cancer

Oct. 25, 2022
By Doris Yu
Suzhou Zelgen Biopharmaceuticals Co. Ltd. reported a phase III trial testing the company’s deuterium-substituted sorafenib derivative donafenib in patients with progressive locally advanced or metastatic radioactive iodine-refractory differentiated thyroid cancer met its primary endpoint following a preplanned interim analysis which found the drug significantly prolonged median progression-free survival vs. a placebo.
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Eucure out-licenses anti-OX40 MAb to Syncromune for intratumoral immunotherapy

Oct. 25, 2022
By Doris Yu
Biocytogen Pharmaceuticals Co. Ltd. subsidiary Eucure Biopharma Co. Ltd. has formed a partnership with Syncromune Inc. to combine Eucure’s YH-002 and two other active ingredients with Syncromune’s Syncrovax platform technology.
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Inxmed collaborates with Huaota to develop combination therapy for solid tumors

Oct. 25, 2022
By Doris Yu
Inxmed Co. Ltd. has formed a partnership with Shanghai Huaota Biopharmaceutical Co. Ltd. to combine the former’s IN-10018 and the latter’s HB-0030 for the treatment of solid tumors by jointly running preclinical studies and clinical trials.
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Zelgen’s donafenib garners positive phase III data in differentiated thyroid cancer

Oct. 24, 2022
By Doris Yu
Suzhou Zelgen Biopharmaceuticals Co. Ltd. reported a phase III trial testing the company’s deuterium-substituted sorafenib derivative donafenib in patients with progressive locally advanced or metastatic radioactive iodine-refractory differentiated thyroid cancer met its primary endpoint following a preplanned interim analysis which found the drug significantly prolonged median progression-free surviva vs. a placebo.
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Inxmed collaborates with Huaota to develop combination therapy for solid tumors

Oct. 20, 2022
By Doris Yu
Inxmed Co. Ltd. has formed a partnership with Shanghai Huaota Biopharmaceutical Co. Ltd. to combine the former’s IN-10018 and the latter’s HB-0030 for the treatment of solid tumors by jointly running preclinical studies and clinical trials.
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Close-up of elderly eye

Usights’s microcatheter is China’s first homegrown minimally invasive glaucoma surgery product

Oct. 19, 2022
By Doris Yu
Tianjin Usights Ophthalmology Technology Co. Ltd.’s ophthalmic fiberoptic microcatheter system has been approved by the NMPA for marketing for minimally invasive glaucoma surgery (MIGS) in China. Tianjin, China-based Usights claims this is the first homegrown products for MIGS in China that has been approved.
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Eucure out-licenses anti-OX40 MAb to Syncromune for intratumoral immunotherapy

Oct. 19, 2022
By Doris Yu
Biocytogen Pharmaceuticals Co. Ltd. subsidiary Eucure Biopharma Co. Ltd. has formed a partnership with Syncromune Inc. to combine Eucure’s YH-002 and two other active ingredients with Syncromune’s Syncrovax platform technology in a deal the partners said could be worth “hundreds of millions of U.S. dollars,” including an up-front cash payment of undisclosed value.
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Colorful illustration of the heart

Rainmed wins Australian approval for coronary artery diseases diagnostic

Oct. 18, 2022
By David Ho
Rainmed Medical Ltd.'s coronary angiography-derived fractional flow reserve system (caFFR system) was approved by Australia’s TGA for precision diagnosis of coronary artery diseases.
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Sino Medical’s drug eluting stent approved for vascular stenosis in China

Oct. 18, 2022
By Doris Yu
Sino Medical Sciences Technology Inc. received marketing approval from China’s NMPA for its drug eluting stent system to improve vascular stenosis in patients with localized ischemic heart disease. The product is designed to improve the speed of wound healing and accelerate the recovery of vascular endothelium after stent implantation. It fits vessels with a diameter of 2.25 mm to 4.00 mm and a lesion length of less than or equal to 40 mm.
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