Core Viewpoint - The company reported a revenue of 294 million yuan for the first half of 2025, representing a year-on-year growth of 75.4%, while the loss narrowed to 132 million yuan compared to the same period in 2024, aligning with expectations [1][2]. Development Trends - The pipeline research and development is progressing steadily, with accelerated clinical and registration advancements for core products. Key updates include: 1. OT-1001 (Zhiwei Tai, 0.24% Azelastine Eye Drops) has been approved for commercialization by the National Medical Products Administration, featuring dual mechanisms for anti-allergy and anti-inflammation [1]. 2. OT-101 (Low-concentration Atropine) has completed a two-year administration for all subjects, with the Phase III clinical trial expected to be unblinded by June 2026 [1]. 3. OT-802 (Pilocarpine) has received approval for Phase III clinical trial application, anticipated to start in early 2026, potentially filling a market gap for innovative drugs in the presbyopia field in China [1]. 4. OT-301 (Latanoprost) has achieved primary endpoint indicators in a global multi-center Phase III clinical trial, surpassing Latanoprost, and is a potential BIC lowering intraocular pressure drug [1]. 5. OT-703 (0.19mg Fluocinolone Vitreous Implant) has been approved for real-world research application in Hainan Boao Lecheng and has completed patient enrollment [1]. Commercialization and Sales Network - The company has demonstrated significant commercial synergy, with rapid expansion of its sales network and channel coverage. In the first half of 2025, the company achieved a revenue of 294 million yuan, with substantial growth in ophthalmic product sales due to successful integration of products from Alcon and the contribution of new products like Zhiwei Tai [2]. - The company has established coverage in 21,535 hospitals nationwide, including 2,799 tertiary hospitals, with a commercial team exceeding 290 members, achieving a nationwide commercial network layout [2]. - The company is actively promoting market access for new products like Zhiwei Tai to enhance market share and build the brand influence of OcuVist, creating new growth points for performance [2]. Production System and Localization - The production system is gradually improving, with enhanced local manufacturing capabilities. During the reporting period, six products received production approval, and commercial batch production is progressing smoothly [2]. - The local production of the core product Yushi Ying has entered the review and public announcement stage, marking a breakthrough in supply assurance and cost control [2]. - Leveraging advanced processes and supply chain management at the Suzhou factory, the company's "OcuVist Manufacturing" model is gradually being implemented, which is expected to ensure supply stability and product quality while strengthening scale advantages, potentially improving production efficiency and reducing costs [2]. Profit Forecast and Valuation - The company maintains its profit forecast for 2025 and 2026. The rating of outperforming the industry is upheld, and considering the recent upward adjustment of the sector's valuation, the target price based on DCF has been raised by 35.5% to 10.16 HKD, indicating a 3.4% upside potential compared to the current stock price [2].

Core Viewpoint - Company maintains its earnings forecast for 2025 and 2026, with a target price increase of 35.5% to HKD 10.16, indicating a 3.4% upside potential from the current stock price [1] Group 1: Pipeline Development - The company's pipeline is progressing steadily, with accelerated clinical and registration advancements for core products [2] - OT-1001 has received approval for commercialization, featuring dual mechanisms for allergy and inflammation [2] - OT-101 has completed a two-year dosing period for all subjects, with III phase clinical unblinding expected by June 2026 [2] - OT-802's III phase clinical trial application has been approved, set to start in early 2026, aiming to fill a market gap in innovative drugs for presbyopia [2] - OT-301 has met primary endpoint indicators in a global multi-center III phase clinical trial, surpassing latanoprost, positioning it as a potential BIC lowering eye pressure drug [2] - OT-703 has been approved for real-world research application in Hainan Boao Lecheng, with patient enrollment completed [2] Group 2: Commercialization and Sales Network - In the first half of 2025, the company achieved revenue of CNY 294 million, a 75.4% year-on-year increase, driven by significant growth in ophthalmic product sales [3] - The company has established coverage across 21,535 hospitals, including 2,799 tertiary hospitals, with a commercial team exceeding 290 members [3] - The company is actively promoting market access for new products, enhancing market share and brand influence [3] Group 3: Manufacturing and Supply Chain - The production system is gradually improving, with local manufacturing capabilities being enhanced [4] - Six products have received production approval, and commercial batch production is progressing smoothly [4] - The local production of the core product has entered the review and public announcement stage, indicating advancements in supply assurance and cost control [4] - The company's "OcuManufacturing" model is being implemented, ensuring supply stability and product quality while enhancing production efficiency and reducing costs [4]

Core Viewpoint - The company maintains its earnings forecast for 2025 and 2026, with an upgraded DCF target price of HKD 10.16, reflecting a 35.5% increase and a 3.4% upside potential from the current stock price [1] Pipeline Development - The company's pipeline is progressing steadily, with key products advancing in clinical and registration phases, including: - OT-1001 (Zhiwei Tai) approved for commercialization by the National Medical Products Administration, featuring dual mechanisms for allergy and inflammation [2] - OT-101 (low-concentration atropine) completing a two-year dosing for all subjects, with Phase III clinical unblinding expected by June 2026 [2] - OT-802 (pilocarpine) receiving approval for Phase III clinical trial application, expected to start in early 2026, potentially filling a market gap in innovative drugs for presbyopia [2] - OT-301 (Gepanoprost) achieving primary endpoint in global multi-center Phase III clinical trials, surpassing Latanoprost, and is a potential BIC lowering eye pressure drug [2] - OT-703 (0.19mg fluocinolone vitreous implant) approved for real-world research application in Hainan Boao Lecheng, with patient enrollment completed [2] Commercialization and Sales Network - The company reported a revenue of CNY 294 million for the first half of 2025, a 75.4% year-on-year increase, driven by significant growth in ophthalmic product sales from the Alcon product portfolio and new product launches [3] - The company has established coverage across 21,535 hospitals, including 2,799 tertiary hospitals, with a commercial team exceeding 290 members, achieving a nationwide commercial network layout [3] - The company is actively promoting market access for new products like Zhiwei Tai to enhance market share and brand influence, creating new growth points for performance [3] Production System Enhancement - The company has received production approvals for six products, with commercial batch production progressing smoothly [4] - The localization of the core product Yushi Ying has entered the review and public announcement stage, indicating breakthroughs in supply assurance and cost control [4] - The company's "Oukang Manufacturing" model, leveraging advanced processes and supply chain management from its Suzhou factory, is expected to enhance supply stability and product quality, while improving production efficiency and reducing costs [4]