drugset / Trial / NCT05593497

A Single-Arm Phase II Study of Neoadjuvant Intensified Androgen Deprivation (Leuprolide and Abiraterone Acetate) in Combination With AKT Inhibition (Capivasertib) for High-Risk Localized Prostate Cancer With PTEN Loss

NCT05593497

Phase 2 Recruiting 30 enrolled VA Office of Research and Development
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to learn about how an investigational drug intervention completed before doing prostate surgery (specifically, radical prostatectomy with lymph node dissection) may help in treatment of high risk localized prostate cancers that are most resistant to standard treatments. This is a phase II research study. For this study, capivasertib, the study drug, will be taken with intensified androgen deprivation drugs (iADT; abiraterone and leuprolide) prior to radical prostatectomy. This study drug treatment will be evaluated to see if it is effective in shrinking and destroying prostate cancer tumors prior to surgery and to further evaluate its safety prior to prostate cancer surgery.

Timeline

Start
2024-05-31
Primary completion
2027-05-01
Completion
2027-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Capivasertib Small molecule 400 mg
Background Abiraterone acetate Small molecule 1000 mg Oral

Indications