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中金:维持君实生物(01877)跑赢行业评级 升目标价至36.98港元
智通财经网·2025-08-29 02:16

Core Viewpoint - CICC has downgraded Junshi Biosciences' (01877) 2025 profit forecast from a loss of 6.62 billion to a loss of 9.17 billion, while introducing a 2026 profit forecast of a loss of 3.15 billion, citing the need for further funding for R&D pipeline advancement [1] Group 1: Financial Performance - The company's 1H25 revenue reached 1.168 billion, a year-on-year increase of 46%, with a net loss of 413 million, which is a reduction in loss by 232 million compared to the previous year [2] - The revenue slightly exceeded CICC's expectations, while the reduction in loss was in line with expectations [2] Group 2: Product Sales Growth - Sales revenue of Tuoyi in the domestic market for 1H25 was 954 million, reflecting a year-on-year growth of 42% [3] - Tuoyi has received approval for 12 indications in China and is approved in 40 countries and regions, indicating a gradual realization of its global commercialization value [3] - The company anticipates accelerated global sales of Tuoyi as new indications enter the market and are included in insurance coverage [3] Group 3: Pipeline Development - The company is focusing on the potential of its PD-1/VEGF bispecific antibody (JS207) and DKK1 monoclonal antibody, which are in advanced clinical stages [4] - JS207 is currently in Phase II clinical trials for various cancers and is expected to have a competitive advantage due to its unique molecular design and anti-tumor efficacy [4] - DKK1 monoclonal antibody has shown promising clinical data for colorectal and gastric cancers and is also in Phase II clinical trials [4] Group 4: Innovation and Clinical Research - The company has established a pipeline covering five major therapeutic areas with over 50 innovative products, advancing nearly 30 products in clinical research [5] - Upcoming submissions for market approval are expected for products like subcutaneous Teriprizumab and IL-17 monoclonal antibody, with several others anticipated to enter critical registration clinical trials by 2025 [5]