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2022-03-21

Henlius Published Phase 2 Study Results of Novel anti-PD-1 mAb Serplulimab for the treatment of advanced cervical cancer patients at SGO 2022
2022-03-18

Henlius’ Potential First-in-Class Anti-PD-L1×TIGIT Bispecific Antibody HLX301 IND Approved by NMPA
2022-03-17

Evolving from Biotech to Biopharma, Mapping out the Future
2022-03-16

Henlius 2021 Annual Results: New Record in Performance, Evolving to Biopharma
2022-03-01

汉利康Ⓡ Approved by NMPA for New Indication Differentiated Strategy Benefits a Wider Patient Population
2022-02-23

Henlius Entered into a Collaboration with Getz Pharma to Commercialise Adalimumab Biosimilar 汉达远, Covering 11 Emerging Markets in Asia, Africa and Europe
2022-02-14

First Subject Dosed in the Australia Phase 1 Trial of Henlius' Potential First-In-Class Anti PD-L1×TIGIT Bispecific Antibody
2022-01-28

First Subject Dosed of a Phase 2 Study of Henlius’ Novel Anti-PD-1 mAb Serplulimab Combined with Anti-EGFR mAb HLX07 in First-line EGFR High Expression sqNSCLC Patients
2022-01-27

First Patient Dosed in the Phase 2 Clinical Trial in LCH/ECD of Henlius BRAF Inhibitor HLX208