比如，和誉医药的第二代FGFR小分子抑制剂ABSK061，在降低对FGFR1抑制的同时，保持对FGFR2/3高选择性，理论上安全性更高。在动物模型中，ABSK061的表现优于Infigratinib，目前ABSK061治疗3-12岁ACH儿童患者的2期临床正在进行中。
ACH病因明确，由FGFR3基因的功能获得性突变导致。该基因调控骨骺生长板软骨细胞增殖分化的重要负调节因子，当其持续激活时，长骨生长被抑制，最终形成特征性的四肢短小身材。
，详情可参考搜狗输入法2026
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