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Completed Phase 1 Interventional

Cixutumumab and Doxorubicin Hydrochloride in Treating Patients With Unresectable, Locally Advanced, or Metastatic Soft Tissue Sarcoma

ClinicalTrials.gov ID: NCT00720174

Public ClinicalTrials.gov record NCT00720174. 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, 10:46 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 Phase 1 Study of Doxorubicin and A12 in Advanced Soft Tissue Sarcoma

Brief summary

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

This phase I trial is studying the side effects and best dose of cixutumumab given together with doxorubicin hydrochloride and to see how well they work in treating patients with unresectable, locally advanced, or metastatic soft tissue sarcoma. Monoclonal antibodies, such as cixutumumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy, such as doxorubicin hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving monoclonal antibody cixutumumab together with doxorubicin hydrochloride may kill more tumor cells.

Study identification

NCT ID
NCT00720174
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
30 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 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 31, 2008
Primary completion
Dec 31, 2012
Completion
Not listed
Last update posted
May 16, 2016

Started 2008

United States locations

U.S. sites
13
U.S. states
6
U.S. cities
13
Facility City State ZIP Site status
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
Decatur Memorial Hospital Decatur Illinois 62526
NorthShore University HealthSystem-Evanston Hospital Evanston Illinois 60201
Ingalls Memorial Hospital Harvey Illinois 60426
Joliet Oncology-Hematology Associates Limited Joliet Illinois 60435
Loyola University Medical Center Maywood Illinois 60153
Illinois CancerCare-Peoria Peoria Illinois 61615
Central Illinois Hematology Oncology Center Springfield Illinois 62702
Fort Wayne Medical Oncology and Hematology Inc-Parkview Fort Wayne Indiana 46845
University of Maryland/Greenebaum Cancer Center Baltimore Maryland 21201
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109
Mercy Hospital Saint Louis St Louis Missouri 63141
Froedtert and the Medical College of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00720174, 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 May 16, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00720174 live on ClinicalTrials.gov.

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