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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 Oct 24, 2026, 4:53 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

Brief summary

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

The purpose of this study is to test the safety and effectiveness of an investigational chemotherapy agent in patients with types of advanced cancer referred to as liposarcoma or leiomyosarcoma.

Study identification

NCT ID
NCT00060944
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
271 participants

Conditions and interventions

Interventions

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
May 2003 (Type not available)
Primary completion
May 2008 (Actual)
Completion
May 2008 (Actual)
Last update posted
Sep 8, 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 8, 2014 · Synced Oct 24, 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 public registry record, listed eligibility criteria, and available contact information for NCT00060944 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →