Reliable Quality

Affordable Innovation

Research Progress

In addition to 5 products and 18 indications launched commercially and 1 NDA accepted for review, Henlius has conducted over 20 clinical studies for 15 products and 12 immuno-oncology combination therapies worldwide. HANLIKANG (rituximab injection), the first product of Henlius, has been approved by the National Medical Products Administration (NMPA) as China's first biosimilar. The second product HANQUYOU (trastuzumab, Zercepac® in the EU,Trade names in Australia: Tuzucip® and Trastucip®) is the first Chinese mAb biosimilar approved both in the EU and China, bringing more treatment options to patients with HER2 positive breast and gastric cancer worldwide. In March 2022, the company’s first self-developed innovative monoclonal antibody HANSIZHUANG (serplulimab injection), was launched. It has been approved by the NMPA for the treatment of Microsatellite Instability-High (MSI-H) solid tumors, squamous non-small cell lung cancer (sqNSCLC) and extensive-stage small cell lung cancer (ES-SCLC). Its NDA for the treatment of esophageal squamous cell carcinoma (ESCC) is under review.

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.