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Completed Phase 3 Interventional Results available

An Efficacy and Safety Study for Yondelis (Trabectedin) in Patients With Advanced Relapsed Ovarian Cancer

ClinicalTrials.gov ID: NCT00113607

Public ClinicalTrials.gov record NCT00113607. 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 Jun 26, 2026, 4:33 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

An Open-Label Multicenter Randomized Phase 3 Study Comparing the Combination of DOXIL/CAELYX and YONDELIS With DOXIL/CAELYX Alone in Subjects With Advanced Relapsed Ovarian Cancer

Study identification

NCT ID
NCT00113607
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Industry
Enrollment
672 participants

Conditions and interventions

Conditions

Interventions

  • Trabectedin Drug
  • DOXIL Drug
  • Dexamethasone Drug

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
Mar 31, 2005
Primary completion
Oct 31, 2010
Completion
Oct 31, 2010
Last update posted
Jun 26, 2014

2005 – 2010

United States locations

U.S. sites
28
U.S. states
21
U.S. cities
28
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed Tucson Arizona
Not listed Los Angeles California
Not listed Newport Beach California
Not listed Orange California
Not listed Englewood Colorado
Not listed Stamford Connecticut
Not listed Tampa Florida
Not listed Coeur d'Alene Idaho
Not listed Louisville Kentucky
Not listed New Orleans Louisiana
Not listed Boston Massachusetts
Not listed Minneapolis Minnesota
Not listed St Louis Missouri
Not listed Morristown New Jersey
Not listed New York New York
Not listed Charlotte North Carolina
Not listed Greenville North Carolina
Not listed Winston-Salem North Carolina
Not listed Cleveland Ohio
Not listed Toledo Ohio
Not listed Portland Oregon
Not listed Pittsburgh Pennsylvania
Not listed Greenville South Carolina
Not listed Chattanooga Tennessee
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed Galveston Texas

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 83 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00113607, 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 Jun 26, 2014 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00113607 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →