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Active, not recruiting Phase 3 Interventional Results available

A Study of Niraparib (GSK3985771) Maintenance Treatment in Participants With Advanced Ovarian Cancer Following Response on Front-Line Platinum-Based Chemotherapy

ClinicalTrials.gov ID: NCT02655016

Public ClinicalTrials.gov record NCT02655016. 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 25, 2026, 3:35 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 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Niraparib Maintenance Treatment in Patients With Advanced Ovarian Cancer Following Response on Front-Line Platinum-Based Chemotherapy

Brief summary

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

This study aims to assess efficacy of Niraparib (GSK3985771) as maintenance treatment in participants with Stage III or IV ovarian cancer. Participants must have completed front-line platinum based regimen with complete response (CR) or partial response (PR). Data collection for Secondary Outcome measures is ongoing and the approximate duration of the study will be 7 years.

Study identification

NCT ID
NCT02655016
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tesaro, Inc.
Industry
Enrollment
733 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Jul 11, 2016 (Actual)
Primary completion
May 17, 2019 (Actual)
Completion
May 29, 2026 (Estimated)
Last update posted
Mar 10, 2026

2016 – 2026

United States locations

U.S. sites
47
U.S. states
28
U.S. cities
44
Facility City State ZIP Site status
GSK Investigational Site Tempe Arizona 85284 —
GSK Investigational Site Tucson Arizona 85710 —
GSK Investigational Site Tucson Arizona 85724 —
GSK Investigational Site San Francisco California 94115 —
GSK Investigational Site San Francisco California 94118 —
GSK Investigational Site Santa Rosa California 95403 —
GSK Investigational Site New Haven Connecticut 06510 —
GSK Investigational Site Jacksonville Florida 32224 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Savannah Georgia 31404 —
GSK Investigational Site Geneva Illinois 60555 —
GSK Investigational Site Indianapolis Indiana 46237 —
GSK Investigational Site Indianapolis Indiana 46260 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Covington Louisiana 70433 —
GSK Investigational Site New Orleans Louisiana 70121 —
GSK Investigational Site Baltimore Maryland 21215-5271 —
GSK Investigational Site Rockville Maryland 20910 —
GSK Investigational Site Burlington Massachusetts 01805 —
GSK Investigational Site Grand Rapids Michigan 49503 —
GSK Investigational Site Minneapolis Minnesota 55433 —
GSK Investigational Site Springfield Missouri 97477 —
GSK Investigational Site Neptune City New Jersey 07753 —
GSK Investigational Site Harrison New York 10604 —
GSK Investigational Site Mineola New York 11501 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site Rochester New York 14620 —
GSK Investigational Site Chapel Hill North Carolina 27599-7570 —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Columbus Ohio 43210 —
GSK Investigational Site Oklahoma City Oklahoma 73104 —
GSK Investigational Site Tulsa Oklahoma 74146 —
GSK Investigational Site Portland Oregon 97210 —
GSK Investigational Site Philadelphia Pennsylvania 19104 —
GSK Investigational Site Willow Grove Pennsylvania 19090 —
GSK Investigational Site Providence Rhode Island 02905 —
GSK Investigational Site Charleston South Carolina 29425 —
GSK Investigational Site Sioux Falls South Dakota 57105 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site The Woodlands Texas 77380 —
GSK Investigational Site Tyler Texas 75701 —
GSK Investigational Site Salt Lake City Utah 84112 —
GSK Investigational Site Kennewick Washington 99336 —
GSK Investigational Site Seattle Washington 98104 —
GSK Investigational Site Spokane Washington 99202 —
GSK Investigational Site Milwaukee Wisconsin 53226 —

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 69 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02655016, 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 Mar 10, 2026 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02655016 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →