Nanjing Leads Biolabs Receives NMPA IND Approval for LBL-047

Reuters12-01

Nanjing Leads Biolabs Receives NMPA IND Approval for LBL-047

Nanjing Leads Biolabs Co. Ltd. announced that its self-developed drug candidate LBL-047 has received Investigational New Drug $(IND)$ approval from the National Medical Products Administration (NMPA) of China. LBL-047 is notable for being the world's first bispecific fusion protein combining a humanized anti-BDCA2 antibody and an engineered TACI ectodomain to receive IND approval in both China and the United States. The approved clinical trial will be a double-blind, randomized, placebo-controlled study. There are currently no approved clinical trials globally targeting both plasmacytoid dendritic cells (pDCs) and B cells, positioning LBL-047 as a strong first and best-in-class candidate. The approval is specific to Nanjing Leads Biolabs Co. Ltd.

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. Nanjing Leads Biolabs Co. Ltd. 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-20251201-11935524), on December 01, 2025, and is solely responsible for the information contained therein.

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