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Completed Phase 2 Interventional Results available

A Study to Assess Treatment With 2 Different Dosing Schedules of Trabectidin Administered to Patients With Advanced Cancer

ClinicalTrials.gov ID: NCT00060944

Public ClinicalTrials.gov record NCT00060944. 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 Jul 21, 2026, 6:44 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, Multicenter, Open-label Study of Yondelis (ET-743 Ecteinascidin) Administered by 2 Different Schedules (Weekly for 3 of 4 Weeks vs. q3 Weeks) in Subjects With Locally Advanced or Metastatic Liposarcoma or Leiomyosarcoma Following Treatment With an Anthracycline and Ifosfamide

Study identification

NCT ID
NCT00060944
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Industry
Enrollment
271 participants

Conditions and interventions

Interventions

  • Yondelis Drug
  • Dexamethasone Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Apr 30, 2003
Primary completion
Apr 30, 2008
Completion
Apr 30, 2008
Last update posted
Sep 7, 2014

2003 – 2008

United States locations

U.S. sites
20
U.S. states
19
U.S. cities
20
Facility City State ZIP Site status
Not listed Los Angeles California
Not listed Aurora Colorado
Not listed Coeur d'Alene Idaho
Not listed Park Ridge Illinois
Not listed Indianapolis Indiana
Not listed Louisville Kentucky
Not listed Boston Massachusetts
Not listed Ann Arbor Michigan
Not listed Minneapolis Minnesota
Not listed Rochester Minnesota
Not listed Newark New Jersey
Not listed New York New York
Not listed Cleveland Ohio
Not listed Portland Oregon
Not listed Philadelphia Pennsylvania
Not listed Nashville Tennessee
Not listed Houston Texas
Not listed Salt Lake City Utah
Not listed Seattle Washington
Not listed 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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00060944, 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 Sep 7, 2014 · Synced Jul 21, 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 NCT00060944 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →