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BioWorld - Tuesday, February 10, 2026
Home » Topics » Regulatory » NMPA

NMPA
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IPO, coins, financial chart

Genfleet raises $234M with Hong Kong IPO

Sep. 19, 2025
By Marian (YoonJee) Chu
No Comments
Genfleet Therapeutics (Shanghai) Inc. debuted on the Hong Kong Stock Exchange on its second attempt at an IPO, raising HK$1.819 billion (US$234 million). Genfleet’s shares (HKEX:2595) rose to HK$44.00 at the opening bell on Sept. 19 and closed at HK$42.10, about 106% higher than the listing price.
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3D map of China
Asia-Pacific in the spotlight

China a great AI med-tech market, but premarket review unpredictable

Sep. 17, 2025
By Mark McCarty
China’s National Medical Products Administration is arguably more active than regulatory agencies in many nations in advancing guidance for AI in medical technology, but Chang-Hong Whitney, President/CEO of Whitney Consulting Ltd., told BioWorld that the premarket review process still carries some unpredictability.
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Colorized scanning electron micrograph of human respiratory syncytial virus.
Infection

CSPC’s SYH-2066 gains trial clearance in China for RSV

Sep. 15, 2025
No Comments
CSPC Pharmaceutical Group Ltd.’s SYH-2066 tablets has obtained clearance from China’s National Medical Products Administration (NMPA) to enter clinical trials for respiratory infections caused by respiratory syncytial virus (RSV).
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Globe isolated on white background with focus on Asia and Australia

Malaysia MDA strengthens regulatory ties with Singapore, China

Aug. 26, 2025
By Marian (YoonJee) Chu
The Medical Device Authority of Malaysia reported on Aug. 22 the piloting of a bilateral medical device approval program with Singapore to streamline the review and launch of medical devices in both countries.
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Remegen’s telitacicept meets phase III endpoints in Sjögren's

Aug. 19, 2025
By Tamra Sami
No Comments
Remegen Co. Ltd.’s telitacicept (RC-18) met the primary endpoint in a phase III trial for treating primary Sjögren's syndrome (pSS), and the company plans to submit a BLA to China’s National Medical Products Administration (NMPA) on the data.
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Remegen’s telitacicept meets phase III endpoints in Sjögren's

Aug. 15, 2025
By Tamra Sami
No Comments
Remegen Co. Ltd.’s telitacicept (RC-18) met the primary endpoint in a phase III trial for treating primary Sjögren's syndrome (pSS), and the company plans to submit a BLA to China’s National Medical Products Administration (NMPA) on the data.
Read More
Floating antibody drug conjugates

Minghui closes $131M pre-IPO round for PD-1/VEGF antibody, ADCs

Aug. 12, 2025
By Marian (YoonJee) Chu
No Comments
Minghui Pharmaceutical Ltd. announced it is raising $131 million in a pre-IPO financing round Aug. 7. The funds will be used to advance its cancer and inflammatory disease pipeline, which include a PD-1/VEGF bispecific antibody, antibody-drug conjugates (ADCs) and a topical Janus kinase inhibitor.
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Aphranel Magiccrystal CaHA filler

China’s Moyom Bio goes global in dermal filler market

Aug. 8, 2025
By Tamra Sami
Shanghai Moyom Biotechnology Co. Ltd. has launched its Aphranel Magiccrystal dermal filler, the first injectable calcium hydroxylapatite microsphere-based dermal filler developed in China, and the company is already expanding globally.
Read More
Floating antibody drug conjugates

Minghui closes $131M pre-IPO round for PD-1/VEGF antibody, ADCs

Aug. 8, 2025
By Marian (YoonJee) Chu
No Comments
Minghui Pharmaceutical Ltd. announced it is raising $131 million in a pre-IPO financing round Aug. 7. The funds will be used to advance its cancer and inflammatory disease pipeline, which include a PD-1/VEGF bispecific antibody, antibody-drug conjugates (ADCs) and a topical Janus kinase inhibitor.
Read More
GLP-1 receptor, inactive form vs. active complex with an agonist (semaglutide) and G-proteins
Endocrine/metabolic

Innovent gets IND for oral GLP-1 agonist

Aug. 5, 2025
No Comments
The U.S. FDA has approved Innovent Biologics, Inc.’s IND application to initiate a phase I clinical trial of its oral GLP-1R agonist IBI-3032.
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