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Terminated Phase 2 Interventional

A Study of DNIB0600A in Comparison With Pegylated Liposomal Doxorubicin (PLD) in Participants With Platinum-Resistant Ovarian Cancer (PROC)

ClinicalTrials.gov ID: NCT01991210

Public ClinicalTrials.gov record NCT01991210. 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 27, 2026, 3:15 PM 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 Randomized, Open-Label, Multicenter, Phase II Trial Evaluating the Safety and Activity of DNIB0600A Compared to Pegylated Liposomal Doxorubicin Administered Intravenously to Patients With Platinum-Resistant Ovarian Cancer

Brief summary

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

This randomized, multicenter, open-label study will evaluate the safety and efficacy of DNIB0600A (RO5541081) in comparison with PLD in participants with PROC, primary peritoneal cancer or fallopian tube cancer. Participants will be randomized to receive either DNIB0600A 2.4 milligrams per kilogram (mg/kg) intravenously (IV) every 3 weeks or PLD 40 milligrams per meter-squared (mg/m\^2) IV every 4 weeks.

Study identification

NCT ID
NCT01991210
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
95 participants

Conditions and interventions

Conditions

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
Feb 6, 2014 (Actual)
Primary completion
Aug 17, 2016 (Actual)
Completion
Aug 17, 2016 (Actual)
Last update posted
Aug 21, 2017

2014 – 2016

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
St. Joseph'S Hospital & Medical Center Phoenix Arizona 85013 —
HonorHealth Research Institute - Pima Center Scottsdale Arizona 85258 —
University of California Irvine Medical Center Orange California 92868 —
Florida Cancer Specialists. St. Petersburg Florida 33705 —
Hematology & Oncology Associates Covington Louisiana 70433 —
Johns Hopkins Uni; Oncology Center Baltimore Maryland 21231 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana Farber Cancer Inst. Boston Massachusetts 02115 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Oklahoma University Health Sciences Center Oklahoma City Oklahoma 73104 —
Northwest Cancer Specialists, P.C. Tualatin Oregon 97062 —
Magee Womens Hospital Pittsburgh Pennsylvania 15213 —
Women & Infants Hospital Providence Rhode Island 02905 —
Sarah Cannon Cancer Center Germantown Tennessee 38138 —

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01991210, 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 Aug 21, 2017 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01991210 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →