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Completed Phase 2 Interventional

Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma

ClinicalTrials.gov ID: NCT00073125

Public ClinicalTrials.gov record NCT00073125. 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 3, 2026, 6:38 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 II Randomized Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma

Brief summary

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

The primary objective of this study is to assess the safety and efficacy of ABT-510 in subjects with advanced renal cell carcinoma.

Study identification

NCT ID
NCT00073125
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Abbott
Industry
Enrollment
103 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
Apr 30, 2003
Primary completion
Not listed
Completion
Not listed
Last update posted
Aug 14, 2007

Started 2003

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Virginia G. Piper Cancer Center Scottsdale Arizona 85258
Arizona Cancer Center Tucson Arizona 85724
UCLA School of Medicine Los Angeles California 90024
Clinical Trials and Research Associates Montebello California 90640
The Center for Hematology-Oncology Boca Raton Florida 33486
University of Chicago Medical Center Chicago Illinois 60637
Central indiana Cancer Center Indianapolis Indiana 46227
Kansas City Cancer Centers Southwest Overland Park Kansas 66210
University of Michigan Ann Arbor Michigan 48109
Kansas City Oncology and Hematology Group Kansas City Missouri 64111
Albany Regional Cancer Center Albany New York 12208
Raleigh Hematology Oncology Clinic Cary North Carolina 27511
US Oncology, P.A. Dallas Texas 75246
Texas Cancer Center Fort Worth Texas 66210
Texas Cancer Center Fort Worth Texas 76104
MD Anderson Cancer Center Houston Texas 77030
Baylor College of Medicine Houston Texas

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00073125, 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 Aug 14, 2007 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00073125 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →