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靠着产品上市销售而不是对外授权,百济神州终于在赚钱了
Di Yi Cai Jing· 2025-08-06 11:53
Core Viewpoint - In the first half of 2025, BeiGene achieved a net profit of 450 million yuan, marking its first profit driven by product sales rather than external licensing, primarily due to the sales growth of its self-developed products, Brukinsa (Zebutinib) and Tislelizumab, as well as Amgen's licensed products [1][2]. Financial Performance - In the first half of 2025, BeiGene reported total revenue of 17.518 billion yuan, a year-on-year increase of 46% [1]. - The global sales of Brukinsa reached 12.527 billion yuan, up 56.2% year-on-year, with U.S. sales contributing 8.958 billion yuan, reflecting a 51.7% increase [3]. - Tislelizumab's sales totaled 2.643 billion yuan, growing by 20.6% year-on-year, driven by new patient demand from its inclusion in the Chinese medical insurance [3]. Revenue Guidance and Profitability - BeiGene updated its revenue guidance for 2025, now expecting total revenue between 35.8 billion and 38.1 billion yuan, with a gross margin forecasted to be in the mid-to-high range of 80% to 90% [3]. - The company anticipates positive net cash flow from operating activities after capital expenditures for the year [3]. Product Development and Pipeline - BeiGene plans to conduct multiple concept validation data readouts across a broad product portfolio, with over 20 milestone advancements expected in the next 18 months in both hematological and solid tumor pipelines [3][4]. - The company is advancing its two blood cancer products, BCL2 inhibitor Sotorasib and BTK chimeric degradation-activated compound BGB-16673, which are in Phase 3 clinical trials [4]. Clinical Trials and Regulatory Progress - Sotorasib is being evaluated in global clinical trials, with a focus on its use in combination with Brukinsa for treating relapsed or refractory chronic lymphocytic leukemia and mantle cell lymphoma [5]. - The application for Sotorasib's marketing in China has been accepted and is under priority review, with plans for data readout from Phase 2 trials expected in the second half of 2025 [5].