Table 1.
IPATASERTIB | CAPIVASERTIB | |
---|---|---|
Clinical trial | IPATential | ProCAID |
Phase | III | II |
Number of patients enrolled | 1101 | 150 |
Primary endpoint | rPFS | cPFS |
Stage of the disease | mCRPC | mCRPC |
Association to AKTi | Abiraterone + Prednisolone | Docetaxel + Prednisolone |
Control | Placebo | Placebo |
Primary outcome’s HR | 0.77 (95% CI, 0.61–0.98); p = 0.034 | 0.92 (80% CI, 0.73–1.16); p = 0.32 |
Grade ≥ 3 adverse events | 70% | 62% |
AEs leading to treatment discontinuation | 21% | 23% |
rPFS: radiological progression-free survival; cPFS: composite radiological progression-free survival; AKTi: AKT inhibitor; mCRPC: metastatic castration resistant prostate cancer, HR: Hazard Ratio; AEs: adverse events.