Reliable Quality

Affordable Innovation

Research Progress

Up to date, in addition to 3 products launched commercially and 3 products under NDA review, Henlius has conducted over 20 clinical studies for 11 products and 8 immuno-oncology combination therapies worldwide. 汉利康® (rituximab injection), the first product of Henlius, has been approved by the NMPA as China's first biosimilar in February 2019. The second product 汉曲优® (trastuzumab, Zercepac® in the EU) was launched both in China and the EU in 2020, becoming the first Chinese mAb biosimilar entering both the EU and China market. It will bring more treatment options to patients with HER2 positive breast and gastric cancer worldwide. HLX01 (rituximab injection) indicated for rheumatoid arthritis, HLX04 (bevacizumab injection) and Serplulimab (anti-PD-1 mAb) were accepted for NDA review by the NMPA.

Products in R&D
Generic Name
Study Phase
Potential Indication
Study Phase
Product Pipeline

With the efficient and innovative in-house capabilities, Henlius has developed a diversified and advanced drug pipeline with a focus in the fields of oncology, autoimmune diseases etc.