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BioWorld - Friday, February 13, 2026
Home » Topics » Regulatory » NMPA

NMPA
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China gives thumbs up to Innovent’s taletrectinib for lung cancer

Dec. 23, 2024
By Tamra Sami
China's National Medical Products Administration (NMPA) approved Innovent Biologics Inc.’s NDA for Dovbleron (taletrectinib), a next-generation ROS1 tyrosine kinase inhibitor (TKI), for treating adults with locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC) who have been previously treated with ROS1 TKIs.
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Illustration of monoclonal antibody hovering between doctor's hands
Cancer

Antibody-drug conjugates SYS-6005, SYS-6043 cleared to enter clinic in China

Dec. 23, 2024
CSPC Pharmaceutical Group Ltd. has received clearance from China’s National Medical Products Administration (NMPA) to conduct clinical trials of antibody-drug conjugates (ADCs) SYS-6005 and SYS-6043.
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Blue heart and data grid

China clears Stereotaxis/Microport’s robotic ablation catheter

Dec. 11, 2024
By Marian (YoonJee) Chu
Stereotaxis Inc. and Chinese partner Shanghai Microport EP Medtech Co. Ltd. gained the National Medical Products Administration’s approval of its Magbot magnetic navigation ablation catheter Dec. 9 for use with Stereotaxis’ robotic ablation system to treat drug-resistant cardiac arrhythmias in China.
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Sanbexin sublingual tablets

NMPA clears drugs from Innovent/Hutchmed, Hengrui, Henlius, Luye

Dec. 10, 2024
By Marian (YoonJee) Chu
China’s National Medical Products Administration (NMPA) granted new approvals to several Chinese biopharmaceuticals this week, including expanding indications of four different cancer drugs and clearing one sublingual tablet for stroke.
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Natural killer cell attacking cancer cell
Immuno-oncology

NK-510 approved to enter clinic in US and China

Dec. 9, 2024
Base Therapeutics (Shanghai) Co. Ltd.’s NK-510 cell injection, a zero-off-target base-edited natural killer (NK) cell product, has received approvals to start clinical trials from both the U.S. FDA and China’s NMPA for clinical trials for advanced solid tumors.
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Sanbexin sublingual tablets

NMPA clears drugs from Innovent/Hutchmed, Hengrui, Henlius, Luye

Dec. 5, 2024
By Marian (YoonJee) Chu
China’s National Medical Products Administration (NMPA) granted new approvals to several Chinese biopharmaceuticals this week, including expanding indications of four different cancer drugs and clearing one sublingual tablet for stroke.
Read More
Kelun Biotech rendering of sacituzumab tirumotecan

China approves Kelun-Biotech’s TROP2 ADC for breast cancer

Dec. 3, 2024
By Marian (YoonJee) Chu
Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. won local approval of the first China-made trophoblast cell-surface antigen 2 (TROP2)-targeted antibody-drug conjugate (ADC), sacituzumab tirumotecan, as a third-line therapy for advanced breast cancer.
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Jiuyuang Gene Engineering IPO ceremony

Jiuyuan Gene raises HKD$485M in Hong Kong IPO

Dec. 3, 2024
By Tamra Sami
Hangzhou Jiuyuan Gene Engineering Co. Ltd. raised HKD$485.4 million (US$62.38 million) in a November 28 IPO on the main board of the Hong Kong Stock Exchange (HKEX:2566).
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Jiuyuang Gene Engineering IPO ceremony

Jiuyuan Gene raises HKD$485M in Hong Kong IPO

Dec. 2, 2024
By Tamra Sami
Hangzhou Jiuyuan Gene Engineering Co. Ltd. raised HKD$485.4 million (US$62.38 million) in a November 28 IPO on the main board of the Hong Kong Stock Exchange (HKEX:2566).
Read More
Kelun Biotech rendering of sacituzumab tirumotecan

China approves Kelun-Biotech’s TROP2 ADC for breast cancer

Dec. 2, 2024
By Marian (YoonJee) Chu
Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. won local approval of the first China-made trophoblast cell-surface antigen 2 (TROP2)-targeted antibody-drug conjugate (ADC), sacituzumab tirumotecan, as a third-line therapy for advanced breast cancer.
Read More
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