Core Viewpoint - CITIC Securities reports that Kelun-Biotech's core product, Sacituzumab Govitecan, has received MNC recognition and global development capabilities, enhancing its potential in combination with Merck's Keytruda for ADC+IO applications. The accelerated global development process and imminent domestic commercialization lead to a target price of HKD 592, maintaining a "Buy" rating [1] Group 1: Product Development - Kelun-Biotech announced that its core product TROP2-ADC, Sacituzumab Govitecan, in combination with Pembrolizumab, achieved the primary endpoint in a Phase III clinical trial for PD-L1 positive non-small cell lung cancer (NSCLC) [1] - This trial marks the first positive Phase III study for ADC combined with immune checkpoint inhibitors in the first-line NSCLC setting globally, confirming the treatment potential of Sacituzumab Govitecan [1] Group 2: Pipeline and Market Potential - The positive trial results further validate the combined treatment potential of Sacituzumab Govitecan, alongside its three approved indications and multiple ongoing clinical trials, indicating a continuous realization of pipeline value [1]