Core Insights - The company has signed a licensing agreement with Pfizer for the PD1×VEGF dual antibody SSGJ707, granting Pfizer global rights (excluding mainland China) for development, production, and commercialization, with an upfront payment of 4.8 billion [1] - The PD1×VEGF dual antibody market is validated, with significant clinical results from competitors enhancing expectations for IO dual antibodies as alternatives to PD1 [2] - The company is expected to achieve substantial revenue growth from its main business, with several late-stage clinical assets projected to generate significant sales [2] Company Developments - The upfront payment of $1.25 billion is the largest for a Chinese innovative drug license out, setting a new record [1] - The company retains a 30% stake in the SSGJ707 project, indicating a strong interest in its future success [1] - The company is positioned as a leader in the domestic autoimmune field, with robust R&D capabilities and a pipeline of clinical assets nearing commercialization [3] Financial Projections - Revenue forecasts for 2025-2027 are projected at 1.37 billion, 1.57 billion, and 1.94 billion yuan, respectively, with net profits expected to be 300 million, 333 million, and 416 million yuan [3] - The company is anticipated to commercialize its IL17 monoclonal antibody by 2025 and submit an NDA for its IL1β monoclonal antibody in the same year, targeting a market with limited competition [2][3]
三生国健(688336):母公司天价DEAL刷记录 临床开发再加速