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Completed Phase 3 Interventional Results available

Phase 3 Study to Compare the Efficacy and Safety of Eribulin With Dacarbazine in Subjects With Soft Tissue Sarcoma

ClinicalTrials.gov ID: NCT01327885

Public ClinicalTrials.gov record NCT01327885. 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 Sep 5, 2026, 12:37 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 3 Study to Compare the Efficacy and Safety of Eribulin With Dacarbazine in Subjects With Soft Tissue Sarcoma

Brief summary

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

This is a randomized, open-label, multicenter, Phase 3 study comparing the efficacy and safety of eribulin with dacarbazine in subjects with advanced soft tissue sarcoma who have disease progression within 6 months prior to study enrolment following standard therapies which must have included an anthracycline, unless contraindicated and then at least one additional regimen after failure of the anthracycline.

Study identification

NCT ID
NCT01327885
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eisai Inc.
Industry
Enrollment
452 participants

Conditions and interventions

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
Mar 9, 2011
Primary completion
Jan 1, 2015
Completion
Aug 9, 2016
Last update posted
Jun 21, 2023

2011 – 2016

United States locations

U.S. sites
30
U.S. states
21
U.S. cities
30
Facility City State ZIP Site status
Not listed Tucson Arizona
Not listed Los Angeles California
Not listed Orange California
Not listed Santa Monica California
Not listed Stanford California
Not listed Aurora Colorado
Not listed Denver Colorado
Not listed Newark Delaware
Not listed Washington D.C. District of Columbia
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Post Falls Idaho
Not listed Chicago Illinois
Not listed Park Ridge Illinois
Not listed Urbana Illinois
Not listed Iowa City Iowa
Not listed Boston Massachusetts
Not listed St Louis Missouri
Not listed Newark New Jersey
Not listed Buffalo New York
Not listed New York New York
Not listed Rochester New York
Not listed Durham North Carolina
Not listed Cleveland Ohio
Not listed Portland Oregon
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Houston Texas
Not listed Burlington Vermont
Not listed Seattle Washington

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 89 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01327885, 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 21, 2023 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01327885 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →