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Completed Phase 2 Interventional Results available

An Efficacy and Safety Study of Niraparib in Men With Metastatic Castration-Resistant Prostate Cancer and DNA-Repair Anomalies

ClinicalTrials.gov ID: NCT02854436

Public ClinicalTrials.gov record NCT02854436. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Efficacy and Safety Study of Niraparib in Men With Metastatic Castration-Resistant Prostate Cancer and DNA-Repair Anomalies

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the efficacy, safety, and pharmacokinetics of niraparib in men with metastatic castration-resistant prostate cancer (mCRPC) and deoxyribonucleic acid (DNA) repair anomalies.

Study identification

NCT ID
NCT02854436
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
289 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2016 (Actual)
Primary completion
Jan 26, 2021 (Actual)
Completion
Aug 16, 2023 (Actual)
Last update posted
Dec 22, 2025

2016 – 2023

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
Not listed Tucson Arizona — —
Not listed Los Angeles California — —
Not listed Riverside California — —
Not listed Sacramento California — —
Not listed Aurora Colorado — —
Not listed Denver Colorado — —
Not listed Evanston Illinois — —
Not listed Danville Kentucky — —
Not listed Louisville Kentucky — —
Not listed New Orleans Louisiana — —
Not listed Boston Massachusetts — —
Not listed Detroit Michigan — —
Not listed Omaha Nebraska — —
Not listed New York New York — —
Not listed Durham North Carolina — —
Not listed Lancaster Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Myrtle Beach South Carolina — —
Not listed Houston Texas — —
Not listed Charlottesville Virginia — —
Not listed Fairfax Virginia — —
Not listed Seattle Washington — —
Not listed Madison Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 87 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02854436, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 22, 2025 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02854436 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →