中金表示，信达生物公告心血管和代谢(CVM)领域重磅产品信尔美(玛仕度肽注射液)作为全球首个GCG/GLP-1双受体激动减重药物在国内获批上市。6月30日，公司举办肿瘤创新研发日活动，展示公司在下一代免疫治疗(IO)与下一代抗体偶联药物(ADC)的战略，并分享包括IBI363(PD-1/IL-2)在内的临床进展和数据解读。 中金认为，公司CVM领域今年以来大单品替妥尤单抗、玛仕度肽已经先后兑现，匹康奇拜也有望年内获批上市，早期管线IBI3030等也均有看点；IO领域IBI363有望成为下一代IO重磅单品，ADC平台不断收获。中金认为公司自后PD-1时代转型顺利，CVM+IO领域管线丰富，有潜力解锁其全球创新价值。 该行基本维持信达生物2025年及2026年归母净利润预测4.72亿元/12.99亿元不变。考虑到玛仕度肽获批上市，创新管线国际化推进，基于现金流量折现法(DCF)模型，上调目标价38.1%至95.3港元。
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