Mei Ri Jing Ji Xin Wen·2025-11-06 16:25Core Viewpoint - BeiGene, a leading innovative pharmaceutical company in China, reported significant financial growth in Q3 2025, with total revenue reaching 27.595 billion yuan, a year-on-year increase of 44.2%, and a net profit of 1.139 billion yuan, recovering from a loss of 368.7 million yuan in the same period last year [2][4]. Financial Performance - Total revenue for the reporting period was 10,076.964 million yuan, reflecting a 41.1% increase compared to the same period last year [3]. - Product revenue amounted to 9,953.836 million yuan, up 40.6% year-on-year, contributing over 98% to total revenue [4]. - The company achieved a total profit of 746.452 million yuan, with a net profit attributable to shareholders of 688.812 million yuan [3]. Product Performance - The core growth drivers for BeiGene's performance were the sales of its BTK inhibitor, Brukinsa (Zebutinib), and the PD-1 monoclonal antibody, Tislelizumab [3][4]. - In Q3, Brukinsa generated global sales of 74.23 billion yuan, a 51.0% increase, accounting for over 70% of the company's product revenue [4]. - The U.S. remained the largest market for Brukinsa, with sales of 52.66 billion yuan, up 46.9%, while European sales surged by 68.2% to 11.65 billion yuan [4]. Market Outlook - The company has adjusted its 2025 revenue forecast, raising the expected range from 35.8 billion to 38.1 billion yuan to 36.2 billion to 38.1 billion yuan [4]. - Research and development expenses, along with sales and management costs, have been narrowed from 29.5 billion to 31.9 billion yuan to 29.5 billion to 30.9 billion yuan [4]. Pipeline Development - BeiGene is advancing its next-generation self-developed pipeline products globally, with the film-coated tablet formulation of Brukinsa approved by the European Commission [5]. - The company plans to submit a marketing application for Brukinsa for marginal zone lymphoma in Japan in the first half of 2026, aiming for orphan drug designation [5]. - The company has also initiated the first patient enrollment for the Phase III clinical trial of Tislelizumab for gastric cancer and submitted a marketing application in Japan [5].