The present invention relates to a FoxM1 gene splicing modifier selected from a compound of formula (I) or of formula (VI)
wherein A and B are as defined herein, or a pharmaceutically acceptable salt thereof, for use in the treatment, prevention and/or delay of progression of cancer.
本发明涉及一种选自式(I)或式(VI)化合物的 FoxM1
基因剪接修饰剂
其中 A 和 B 如本文所定义,或其药学上可接受的盐,用于治疗、预防和/或延缓癌症进展。