FOSUN PHARMA announced that its subsidiary, Shanghai Henlius Biotech, Inc., along with its controlled subsidiaries, has received approval for the Phase I clinical trial protocol of its self-developed HLX3902 injection (a STEAP1xCD3xCD28 trispecific antibody) intended for the treatment of metastatic castration-resistant prostate cancer and other advanced solid tumors. The protocol has been approved by the relevant human research ethics committee and has passed the filing with Australia's Therapeutic Goods Administration. This marks the first global clinical trial approval for this drug candidate. Henlius plans to initiate the related clinical studies in Australia once the necessary conditions are met.
Comments