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Terminated Phase 2Phase 3 Interventional Results available

Study of Combretastatin and Paclitaxel/Carboplatin in the Treatment of Anaplastic Thyroid Cancer

ClinicalTrials.gov ID: NCT00507429

Public ClinicalTrials.gov record NCT00507429. 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 21, 2026, 2:22 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 Phase II/III Study to Evaluate the Safety and Efficacy of Combretastatin A-4 Phosphate in Combination With Paclitaxel and Carboplatin in Comparison With Paclitaxel and Carboplatin Against Anaplastic Thyroid Carcinoma [FACT]

Brief summary

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

The purpose of the study is to determine the safety and efficacy of combretastatin combined with paclitaxel and carboplatin in the treatment of anaplastic thyroid cancer (ATC).

Study identification

NCT ID
NCT00507429
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Mateon Therapeutics
Industry
Enrollment
80 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
Aug 2007 (Type not available)
Primary completion
Oct 2011 (Actual)
Completion
Nov 2011 (Actual)
Last update posted
Jun 9, 2014

2007 – 2011

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
USC/Norris Comprehensive Cancer Center Los Angeles California 90033 —
University of Colorado Cancer Center Aurora Colorado 80045 —
Yale University, School of Medicine New Haven Connecticut 06520 —
Winship Cancer Institute, Emory University Atlanta Georgia 30322 —
Sidney Kimmel Comprehensive Cancer Care Center at John Hopkins Baltimore Maryland 21231 —
University of Minnesota Otolaryngology Department Minneapolis Minnesota 55455 —
Ireland Cancer Center/Division od Hematology Cleveland Ohio 44106 —
Oregon Health and Science University Portland Oregon 97239 —
University of Texas M.D. Anderson Cancer Center Houston Texas 77030 —
West Virginia University Morgantown West Virginia 26506 —

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 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00507429, 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 9, 2014 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00507429 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →