OncRef

Clinical Trial: NCT03419234

Abiraterone Acetate and Antiandrogen Therapy With or Without Cabazitaxel and Prednisone in Treating Patients With Metastatic, Castration-Resistant Prostate Cancer Previously Treated With Docetaxel

Status:

ACTIVE NOT RECRUITING

Phase:

Phase 2

Lead Sponsor:ECOG-ACRIN Cancer Research Group
Information Provided By:Eastern Cooperative Oncology Group
Last Update Posted:2026-10-06

Study Overview

Brief Summary

This randomized phase II trial studies how well abiraterone acetate and antiandrogen therapy, with or without cabazitaxel and prednisone, work in treating patients with castration-resistant prostate cancer previously treated with docetaxel that has spread to other parts of the body. Androgens can cause the growth of prostate cancer cells. Hormone therapy using abiraterone acetate and antiandrogen therapy may fight prostate cancer by lowering and/or blocking the use of androgens by the tumor cells. Drugs used in chemotherapy, such as cabazitaxel and prednisone, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving abiraterone acetate and antiandrogen therapy with or without cabazitaxel and prednisone may help kill more tumor cells.

Official Title

Cabazitaxel With Abiraterone Versus Abiraterone Alone Randomized Trial for Extensive Disease Following Docetaxel: The CHAARTED2 Trial

Conditions

Castration Levels of Testosterone, Castration-Resistant Prostate Carcinoma, Metastatic Prostate Carcinoma in the Soft Tissue, Prostate Carcinoma Metastatic in the Bone, Stage IV Prostate Adenocarcinoma AJCC v7

Intervention / Treatment

  • Drug: Abiraterone Acetate
  • Drug: Androgen deprivation therapy
  • Drug: Cabazitaxel
  • Drug: Prednisone

Other Study ID Numbers

  • EA8153
  • NCI-2017-00389
  • EA8153
  • EA8153
  • U10CA180820

Start Date (Actual)

2018-04-26

Primary Completion Date (Actual)

2024-01-08

Study Completion Date (Estimated)

2028-04-01

Enrollment (Actual)

223

Study Type

Interventional

Phase

Phase 2