BAT2306

Search documents
百奥泰生物制药股份有限公司2025年半年度业绩预告的自愿性披露公告
Shang Hai Zheng Quan Bao· 2025-07-29 17:36
Group 1 - The company expects a net loss attributable to shareholders of the parent company for the first half of 2025 to be between -110 million and -140 million yuan, representing a reduction in loss of 96.84 million to 126.84 million yuan compared to the same period last year [2] - The expected net loss attributable to shareholders after deducting non-recurring gains and losses is projected to be between -160 million and -190 million yuan, indicating a reduction in loss of 80.33 million to 110.33 million yuan [2] - The previous year's net loss attributable to shareholders was -236.85 million yuan, with a net loss after deducting non-recurring gains and losses of -270.33 million yuan [4] Group 2 - The company anticipates a decrease in losses due to increased market expansion, with sales of Adalimumab injection (Geleli) expected to rise, contributing an additional revenue of 20 million to 50 million yuan compared to the previous year [6] - Research and development expenses are expected to decrease by 40 million to 70 million yuan compared to the previous year, primarily because several R&D projects have completed Phase III clinical trials, with BAT2206, BAT2306, and BAT2506 currently in the application stage for market approval [6] - BAT2206 has already received FDA approval for market launch in the United States, which has contributed to the reduction in R&D expenses [6]
百奥泰上半年业绩显著改善 预计减亏超亿元
Zheng Quan Ri Bao· 2025-07-29 13:40
Core Insights - The company, Baiotai Biopharmaceutical Co., Ltd., reported a significant reduction in losses for the first half of 2025, with expected net losses between 1.1 billion to 1.4 billion yuan, a decrease of 970 million to 1.27 billion yuan compared to the same period last year [2] - The sales of the company's first approved biosimilar, Adalimumab Injection (brand name: Geleli®), have contributed to an increase in operating revenue by 20 million to 50 million yuan year-on-year, showcasing the effectiveness of the company's commercialization team [2] - Research and development expenses decreased by 40 million to 70 million yuan during the reporting period, indicating improved cost structure and efficiency [2] Financial Performance - The expected net profit for the first half of 2025 is projected to be between -1.1 billion to -1.4 billion yuan, reflecting a significant narrowing of losses compared to the previous year [2] - The increase in operating revenue is attributed to the successful commercialization of core products, particularly the sales growth of the Adalimumab Injection [2] R&D and Market Strategy - The company has achieved a milestone with the FDA approval of BAT2206, which is crucial for its international strategy [2] - BAT2306 and BAT2506 are currently in the application stage for market approval, indicating a robust pipeline for future growth [2] - The dual focus on biosimilars and innovative drugs is expected to provide strong momentum for the company's long-term development [2]
百奥泰上半年净利预亏1.1亿元至1.4亿元,同比减亏
Bei Jing Shang Bao· 2025-07-29 13:28
Core Viewpoint - Baiotai (688177) is expected to reduce its losses in the first half of 2025, with a projected net profit attributable to shareholders ranging from -110 million to -140 million yuan, indicating a decrease in losses by 96.8458 million to 127 million yuan compared to the previous year [1] Financial Performance - The company anticipates a reduction in losses for the reporting period compared to the same period last year [1] - Revenue from the sales of Adalimumab injection (Geleli) is expected to increase by 20 million to 50 million yuan year-on-year [1] Research and Development - R&D expenses are projected to decrease by 40 million to 70 million yuan compared to the previous year [1] - The reduction in R&D costs is attributed to the completion of several global Phase III clinical trials, with projects BAT2206, BAT2306, and BAT2506 currently in the application stage for market approval [1] - BAT2206 has already received approval from the US FDA for market launch [1]