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Completed Phase 3 Interventional Results available

A Study Comparing the Combination of Trabectedin (YONDELIS) and DOXIL/CAELYX With DOXIL/CAELYX for the Treatment of Advanced-Relapsed Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancer

ClinicalTrials.gov ID: NCT01846611

Public ClinicalTrials.gov record NCT01846611. 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 22, 2026, 5:04 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 Randomized, Open-Label Study Comparing the Combination of YONDELIS and DOXIL/CAELYX With DOXIL/CAELYX Monotherapy for the Treatment of Advanced-Relapsed Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancer

Brief summary

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

The purpose of this study is to assess the efficacy and safety of trabectedin+DOXIL as a third-line chemotherapy regimen (treatment) in patients with platinum-sensitive advanced-relapsed epithelial ovarian, primary peritoneal, or fallopian tube cancer who received 2 previous lines of platinum-based chemotherapy.

Study identification

NCT ID
NCT01846611
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
581 participants

Conditions and interventions

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
Oct 16, 2013 (Actual)
Primary completion
Jan 18, 2018 (Actual)
Completion
Nov 16, 2018 (Actual)
Last update posted
Apr 1, 2019

2013 – 2018

United States locations

U.S. sites
75
U.S. states
32
U.S. cities
75
Facility City State ZIP Site status
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Not listed San Antonio Texas — —
Not listed The Woodlands Texas — —
Not listed Webster Texas — —
Not listed Salt Lake City Utah — —
Not listed Annandale Virginia — —
Not listed Newport News Virginia — —
Not listed Roanoke Virginia — —
Not listed Spokane Washington — —
Not listed Vancouver Washington — —
Not listed Green Bay Wisconsin — —
Not listed Madison Wisconsin — —
Not listed Milwaukee Wisconsin — —
Not listed Wauwatosa 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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01846611, 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 Apr 1, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01846611 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →