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Active Not RecruitingNCT03732820

Study on Olaparib Plus Abiraterone as First-line Therapy in Men With Metastatic Castration-resistant Prostate Cancer

A Randomised, Double-blind, Placebo-controlled, Multicentre Phase III Study of Olaparib Plus Abiraterone Relative to Placebo Plus Abiraterone as First-line Therapy in Men With Metastatic Castration-resistant Prostate Cancer (PROpel Study)

Status
Active Not Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
895 (actual)
Sponsor
AstraZeneca · Industry
Sex
Male
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety (including evaluating side effects) of combination of olaparib and abiraterone versus placebo and abiraterone in patients with metastatic castration-resistant prostate cancer (mCRPC) who have received no prior cytotoxic chemotherapy or new hormonal agents (NHAs) at metastatic castration-resistant prostate cancer (mCRPC) stage.

Detailed description

PROpel is a phase III study evaluating the efficacy, safety, and tolerability of olaparib versus placebo when given in addition to abiraterone to patients with metastatic castration-resistant prostate cancer (mCRPC) who have not received prior chemotherapy or new hormonal agents (NHAs) for metastatic castration-resistant prostate cancer (mCRPC) (first-line setting). Approximately 720 patients globally were planned to be randomized in PROpel in a 1:1 ratio to treatment with either olaparib and abiraterone or placebo and abiraterone. Enrolment had completed with a total of 796 patients randomised. Following the completion of global enrolment, the China cohort will randomise approximately 108 additional patients at sites in China, also in a 1:1 ratio. Patients will receive oral treatment with olaparib 300 mg twice daily + abiraterone 1000 mg once daily or placebo twice daily + abiraterone 1000 mg once daily. Patients in both treatment groups will also receive either prednisone or prednisolone 5 mg twice daily.

Conditions

Interventions

TypeNameDescription
DRUGolaparib300 mg (2 x 150 milligrams (mg) tablets) twice daily
DRUGabiraterone acetate1000 milligrams (mg) once daily

Timeline

Start date
2018-10-31
Primary completion
2021-07-30
Completion
2026-04-27
First posted
2018-11-07
Last updated
2026-01-29
Results posted
2023-06-15

Locations

132 sites across 17 countries: United States, Australia, Belgium, Brazil, Canada, Chile, Czechia, France, Germany, Italy, Japan, Netherlands, Slovakia, South Korea, Spain, Turkey (Türkiye), United Kingdom

Regulatory

Source: ClinicalTrials.gov record NCT03732820. Inclusion in this directory is not an endorsement.