Table 3.
Phase I-II clinical trials investigating SPRMs for breast cancer prevention.
| Trial | Interventions | Patient characteristics | Results |
|---|---|---|---|
| Mifepristone | |||
| NCT01898312 (123) | mifepristone 50 mg vs. placebo | 45 healthy BRCA1/2 carriers | Reduced mitotic age and proportion of luminal progenitor cells in normal breast tissue |
| Ulipristal acetate | |||
| BC-APPS1 trial (123) | ulipristal acetate 5 mg | 30 high-risk women | Reduced mitotic age and proportion of luminal progenitor cells in normal breast tissue |
| NCT02922127 (124) | ulipristal acetate 10 mg vs. combined oral contraceptive | 25 young normal-risk women | decreased ki-67 proliferation and reduced background parenchymal enhancement of normal breast tissue |
| Telapristone acetate | |||
| NCT02314156 (127) | Oral vs. topical telapristone acetate 12 mg | 60 women undergoing mastectomies | local drug distribution patterns are similar between oral and topical telapristone acetate |