Shanghai Henlius says NMPA approves Hanlikang rituximab indication expansion for DLBCL

Reuters04-09

Shanghai Henlius says NMPA approves Hanlikang rituximab indication expansion for DLBCL

Shanghai Henlius Biotech secured China NMPA clearance to expand HANLIKANG (rituximab) label into two additional diffuse large B-cell lymphoma regimens.
New uses cover first-line DLBCL in combination with polatuzumab vedotin plus chemotherapy, also relapsed or refractory DLBCL in transplant-ineligible adults with bendamustine plus polatuzumab vedotin.
Rituximab injection sales in mainland China totaled about RMB 3.5 billion in 2025, according to IQVIA CHPA.

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-20260409-12100296), on April 09, 2026, and is solely responsible for the information contained therein.

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