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Active, not recruiting Phase 3 Interventional Results available

Olaparib Treatment in BRCA Mutated Ovarian Cancer Patients After Complete or Partial Response to Platinum Chemotherapy

ClinicalTrials.gov ID: NCT01874353

Public ClinicalTrials.gov record NCT01874353. 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 Sep 7, 2026, 1:58 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

Phase III Randomised, Double Blind, Placebo Controlled Study of Olaparib Maintenance Monotherapy in Platinum Sensitive Relapsed BRCA Mutated Ovarian Cancer Patients With a Complete or Partial Response Following Platinum Based Chemotherapy

Brief summary

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

A Phase III, randomised, double-blind, placebo-controlled, multi-centre study to assess the efficacy of olaparib maintenance monotherapy in relapsed high grade serous ovarian cancer (HGSOC) patients (including patients with primary peritoneal and / or fallopian tube cancer) or high grade endometrioid cancer with BRCA mutations (documented mutation in BRCA1 or BRCA2 that is predicted to be deleterious or suspected deleterious (known or predicted to be detrimental/lead to loss of function)) who have responded following platinum based chemotherapy.

Study identification

NCT ID
NCT01874353
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
327 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 130 Years
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
Sep 2, 2013
Primary completion
Sep 18, 2016
Completion
Dec 30, 2026
Last update posted
Jul 28, 2026

2013 – 2026

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama
Palo Alto Foundation Medical Group San Francisco California
University of Colorado Aurora Colorado
The Hospital of Central Connecticut New Britain Connecticut
Gynecologic Cancer Center Orlando Florida
North Shore University Evanston Illinois
Greater Baltimore Medical Center Baltimore Maryland
Johns Hopkins Baltimore Maryland
Dana Farber Cancer Institute Boston Massachusetts
Massachusetts General Hospital Boston Massachusetts
MD Anderson at Cooper Cancer Center Voorhees Township New Jersey
Womens Cancer Care Associates Albany New York
Winthrop Gynecologic Oncology Associates Mineola New York
OSU JamesCare at Mill Run Hilliard Ohio
Henry Joyce Cancer Clinic Nashville Tennessee
Aurora St Lukes Medical Center Milwaukee 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 110 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01874353, 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 Jul 28, 2026 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01874353 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →