申请人:LILLY CO ELI
公开号:WO2022187443A1
公开(公告)日:2022-09-09
The present invention provides compounds of the formula:, for use in the treatment of systemic sclerosis, fibrosis (e.g. pulmonary fibrosis), achondroplasia, thanatophoric dysplasia (e.g. type I), severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), muenke syndrome or cancer.
本发明提供了以下式子的化合物,用于治疗全身性硬化、纤维化(例如肺纤维化)、软骨发育不全症、死亡性发育不良(例如I型)、伴发展迟缓和黑棘皮病的严重软骨发育不全症(SADDAN)、明克氏综合症或癌症。