中金公司发表研报指，荣昌生物日前宣布将尽快就自主研发的BLyS/APRIL双靶点融合蛋白创新药泰它西普，向国家药品监督管理局药品审评中心(CDE)递交上市申请，并在国际重大学术会议上公布详细数据。另外，公司的RC148获得FDA批准在美国开展针对多种晚期恶性实体肿瘤的Ⅱ期临床研究，标志着RC148进入全球临床研发阶段，为推动产品后续开发奠定基础；该行认为RC148具有国际化临床价值和出海潜力。 该行基本维持荣昌生物2025及26年归母净亏损预测9.15亿元及3.33亿元不变。由于泰它西普干燥综合症III期临床结果积极，有望提升泰它西普未来价值空间，且RC148美国II期临床获批有望提升其出海潜力和全球价值空间。该行维持公司“跑赢行业”评级，上调目标价24.8%至95.34港元。
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