China NMPA approves Shanghai Henlius IND for HLX3901 phase 1 trial in advanced solid tumours

Reuters03-09

China NMPA approves Shanghai Henlius IND for HLX3901 phase 1 trial in advanced solid tumours

Shanghai Henlius said China’s National Medical Products Administration approved its investigational new drug application for a Phase 1 clinical trial of HLX3901 injection in advanced or metastatic solid tumours. HLX3901 is a DLL3xDLL3xCD3xCD28 tetra-specific antibody. Henlius said no comparable tetra-specific antibody targeting DLL3 dual epitopes, CD3 and CD28 has been approved globally.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Shanghai Henlius Biotech Inc. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260309-12045271), on March 09, 2026, and is solely responsible for the information contained therein.

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