FOSUN PHARMA (600196.SH) announced that its subsidiary Shanghai Henlius Biotech, Inc. and its controlled subsidiaries (collectively referred to as "Henlius") recently received approval from the National Medical Products Administration (NMPA) to conduct the following clinical trials in China for HLX22 (a recombinant humanized anti-HER2 monoclonal antibody injection) combined with HLX87 injection (a HER2-targeted antibody-drug conjugate): (1) Phase II/III clinical trials for first-line treatment of HER2-positive breast cancer (BC); (2) Phase II/III clinical trials for HER2-positive breast cancer neoadjuvant therapy (BC neo). Henlius plans to initiate the relevant clinical studies in China once conditions are met.
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