BENITIONSClinical Trial Intelligence

A Study of Niraparib in Combination With Abiraterone Acetate and Prednisone Versus Abiraterone Acetate and Prednisone for Treatment of Participants With Metastatic Prostate Cancer

Фаза 3 Идёт, набор закрыт NCT03748641

ЗаболеваниеCastration-Resistant Prostatic Cancer
ФазаФаза 3
СпонсорJanssen Research & Development, LLC
СтатусИдёт, набор закрыт
Участники765 участн.
ВмешательствоNiraparib, Abiraterone Acetate, Prednisone, New Formulation of Niraparib and Abiraterone Acetate (AA)
Дата начала25.01.2019
Дата завершения8.10.2021
Публикация результатов4.10.2023

Кратко

The purpose of this study is to evaluate the effectiveness of niraparib in combination with abiraterone acetate plus prednisone (AAP) compared to AAP and placebo.

Cohort 1: Radiographic Progression-Free Survival (rPFS) as Assessed by Blinded Independent Central Review (BICR)

Up to 32 months · Months

Cohort 1: Niraparib 200 mg + Abiraterone Acetate 1000 mg + Prednisone 10 mg16.46 Months
Cohort 1: Placebo + Abiraterone Acetate 1000 mg + Prednisone 10 mg13.70 Months
p-value0.0217
Hazard Ratio (HR)0.729 (95% CI 0.556–0.956)

Cohort 1 Breast Cancer Gene (BRCA) Subgroup: Radiographic Progression-Free Survival (rPFS) as Assessed by Blinded Independent Central Review (BICR)

Up to 32 months · Months

Cohort 1 BRCA Subgroup: Niraparib 200 mg + Abiraterone Acetate 1000 mg + Prednisone 10 mg16.56 Months
Cohort 1 BRCA Subgroup: Placebo + Abiraterone Acetate 1000 mg + Prednisone 10 mg10.87 Months
p-value0.0014
Hazard Ratio (HR)0.533 (95% CI 0.361–0.789)

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