Group 1 - The company achieved a revenue of 950 million yuan in H1 2025, a year-on-year decrease of 31.3%, primarily due to high milestone payments recognized in the same period of 2024 [1] - The net loss attributable to the parent company was 145 million yuan, with an adjusted net loss of 69 million yuan [1] - The pharmaceutical sales revenue reached 309.8 million yuan, with sac-TMT accounting for 97.6% of total pharmaceutical sales, indicating successful commercialization progress [1][2] Group 2 - The sales revenue from sac-TMT is mainly derived from second-line triple-negative breast cancer and third-line EGFR mutation NSCLC, with the second-line EGFR mutation NSCLC indication expected to be approved in China soon, potentially driving stronger annual sales growth [2] - Sac-TMT's two approved indications will participate in the 2025 medical insurance negotiations, with expectations for accelerated sales growth after entering the insurance directory in 2026 [2] - Multiple clinical data will be disclosed at the ESMO conference in H2 2025, including phase III data for sac-TMT in second-line EGFR mutation NSCLC and phase I data for SKB315 (CLDN18.2 ADC) [2] Group 3 - The company's other core product, HER2 ADC (Bodutuzumab), received NDA acceptance in January 2025 and is expected to be approved for market launch in H2 2025 [3] - The company plans to submit the NDA application for the next-generation RET inhibitor A400 in H2 2025 [3] - The next major product, SKB571/MK-2750 (dual antibody ADC), is set to begin phase II clinical trials in China soon [3]