必贝特：专注创新药自主研发 力争成为具有国际竞争力的生物制药企业

Company Overview - Guangzhou Bibetter Pharmaceutical Co., Ltd. is a biopharmaceutical company established in 2012, focusing on innovative drug research and development with a clinical value orientation [4] - The company specializes in major disease areas such as tumors and metabolic diseases, leveraging its core technology platform for continuous development of first-in-class drugs and innovative medicines addressing unmet clinical needs [4][11] Research and Development Pipeline - The company has established a diverse and differentiated R&D pipeline, having obtained over 30 clinical approvals, with one class 1 innovative drug already on the market and two others in phase III clinical trials [5][21] - The core product, BEBT-908, is a globally first-in-class HDAC/PI3Kα dual-target anti-tumor drug, approved for treating relapsed or refractory diffuse large B-cell lymphoma, with other indications in phase II clinical trials [5][25] - The company is also focusing on next-generation small nucleic acid (siRNA) drug development, having established three proprietary delivery systems with global intellectual property rights [6][22] Financials and Investment - The company has invested significantly in R&D, with expenditures of approximately 166.74 million yuan in 2022, 157.65 million yuan in 2023, and projected 120.29 million yuan in 2024 [17] - The funds raised from the IPO will primarily be used to accelerate the clinical progress of the R&D pipeline, enhance commercialization capabilities, and expand the product line [26][30] Market Position and Strategy - The company aims to become a globally influential innovative drug developer in major disease areas, focusing on deepening independent R&D, accelerating commercialization, and expanding into global markets [19] - The competitive advantages include innovation-driven development, strong R&D capabilities, a broad product pipeline, and significant market potential for approved and core products [20][25] Regulatory Environment - The implementation of the drug marketing authorization holder (MAH) system is seen as a favorable policy for the company, allowing it to focus resources on core R&D activities [25] - The company meets the listing standards for the Sci-Tech Innovation Board, having at least one core product approved for clinical trials and a projected market value of no less than 4 billion yuan [28][29]