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Withdrawn Phase 2 Interventional

A Study to Evaluate the Effectiveness and Tolerability of a Second Maintenance Treatment in Participants With Ovarian Cancer, Who Have Previously Received Polyadenosine 5'Diphosphoribose [Poly (ADP Ribose)] Polymerase Inhibitor (PARPi) Treatment.

ClinicalTrials.gov ID: NCT04239014

Public ClinicalTrials.gov record NCT04239014. 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 2, 2026, 1:53 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 Randomized, Multi-Centre Study to Investigate the Efficacy and Tolerability of a Second Maintenance Treatment in Patients With Platinum Sensitive Relapsed Epithelial Ovarian Cancer, Who Have Previously Received PARP Inhibitor Maintenance Treatment

Brief summary

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

To investigate the effectiveness and tolerability of a second maintenance treatment in participants with platinum-sensitivity relapsed (PSR) epithelial ovarian cancer, who have previously received PARPi maintenance treatment and who have benefit (complete response \[CR\] or partial response \[PR\]) or stable disease (SD) from further platinum based chemotherapy.

Study identification

NCT ID
NCT04239014
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
Not listed

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
Aug 6, 2020
Primary completion
Jan 24, 2021
Completion
Jan 24, 2021
Last update posted
Mar 9, 2021

2020 – 2021

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Research Site Anchorage Alaska 99508
Research Site La Jolla California 92093-0021
Research Site Long Beach California 90806
Research Site Los Angeles California 90048
Research Site West Hollywood California 97210
Research Site Hartford Connecticut 06106
Research Site Tampa Florida 33612
Research Site Atlanta Georgia 30342
Research Site Louisville Kentucky 40202
Research Site Covington Louisiana 70433
Research Site Florham Park New Jersey 07932
Research Site Teaneck New Jersey 07666
Research Site Cleveland Ohio 44106
Research Site Oklahoma City Oklahoma 73104
Research Site Tulsa Oklahoma 74146
Research Site Portland Oregon 97210
Research Site Abington Pennsylvania 19001
Research Site Philadelphia Pennsylvania 19104
Research Site Sioux Falls South Dakota 57105-1599
Research Site Sioux Falls South Dakota 57105
Research Site Houston Texas 77030
Research Site Seattle Washington 98104

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04239014, 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 9, 2021 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04239014 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →