Ge Long Hui·2026-01-15 21:54Core Viewpoint - The company has signed an exclusive licensing agreement with AbbVie for the PD-1/VEGF dual antibody drug RC148, granting AbbVie exclusive rights for development, production, and commercialization outside Greater China, with an upfront payment of $650 million and potential milestone payments up to $4.95 billion, along with double-digit royalties on net sales outside Greater China [1][2]. Group 1: Licensing Agreement Details - The agreement includes an upfront payment of $650 million and milestone payments that could reach up to $4.95 billion [1]. - AbbVie will have exclusive rights to develop, produce, and commercialize RC148 outside of Greater China [1]. Group 2: Clinical Data and Efficacy - RC148 has shown promising efficacy and safety in recent clinical trials, with a Phase 1 study demonstrating an overall response rate (ORR) of 61.9% and a disease control rate (DCR) of 100% among PD-L1 positive NSCLC patients [1]. - In the Phase 2 study, the combination of RC148 with docetaxel achieved an ORR of 66.7% and a DCR of 95.2%, with an ORR of 80% in PD-L1 positive patients [2]. Group 3: Business Development and Financial Impact - This licensing agreement marks the fourth successful business development (BD) transaction for the company, validating its R&D capabilities and recognition by foreign entities [2]. - The high upfront payment is expected to significantly improve the company's cash flow and provides strong financial and brand endorsement for future R&D and pipeline advancement [2]. Group 4: Profit Forecast - The company anticipates a net profit of -885 million, -449 million, and 373 million yuan for the years 2025 to 2027, with corresponding earnings per share (EPS) of -1.57, -0.80, and 0.66 yuan [2].