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BioWorld - Monday, June 15, 2026
Home » Topics » Regulatory » NMPA

NMPA
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NMPA approves flumatinib mesylate for the treatment of Ph+ chronic myeloid leukemia

Nov. 29, 2019

I-Mab obtains Chinese IND clearance for phase I trials of TJM-2 in rheumatoid arthritis

Nov. 15, 2019

HLX-11 receives IND application acceptance notification from NMPA

Nov. 6, 2019

Oligomannate approved in China for mild to moderate AD

Nov. 4, 2019

NMPA clears I-Mab's IND for China trial of CD73 antibody

Oct. 9, 2019
By David Ho
HONG KONG – I-Mab Biopharma (Shanghai) Co. Ltd. has received IND approval from China's National Medical Products Administration (NMPA) for its CD73 antibody, getting the go-ahead for a phase I/II trial of TJD-5 in patients with advanced solid tumors.
Read More

IP enforcement in China improving slowly but surely

Sep. 25, 2019
By Mark McCarty

China confirms drug reforms to spur innovation, ensure drug quality, ease restrictions

Sep. 10, 2019
By Elise Mak
BEIJING – China has finally written all its drug-related reforms into law, as it passed the amendment of its drug administration law in late August, the amendment to take effect on Dec. 1. Those moves carry one goal: to bring more and better drugs into the Chinese market as quickly as possible.
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China's NMPA approves Focus V for third-line treatment of SCLC

Sep. 6, 2019

China's NMPA approves roxadustat for anemia in patients with CKD not receiving dialysis

Aug. 22, 2019

Ascletis receives IND approval for ASC-18 in China

Aug. 6, 2019
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