As exemplified by the clinical candidates ARV‐110 and ARV‐471, respectively, it has been possible to develop PROTACs against targets previously considered undruggable, including androgen receptor (AR) in prostate cancer and estrogen receptor (ER) in breast cancer, as illustrated in (Figure 2) (Dogheim and Amralla 2023; Snyder et al. 2025). This evidence concerns the gene AR and breast carcinoma.