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Terminated Phase 2 Interventional

AVN944 in Combination With Gemcitabine for the Treatment of Pancreatic Cancer

ClinicalTrials.gov ID: NCT00493441

Public ClinicalTrials.gov record NCT00493441. 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 4, 2026, 5:50 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 Study of AVN944 in Combination With Gemcitabine for the Treatment of Pancreatic Cancer

Brief summary

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

The study was designed to find the optimum AVN944 dose to use in combination with gemcitabine in patients with pancreatic cancer and see if the combination of the 2 drugs was more effective for treating pancreatic cancer than using gemcitabine alone.

Study identification

NCT ID
NCT00493441
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
28 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
Jun 2007 (Type not available)
Primary completion
Dec 2009 (Actual)
Completion
Dec 2009 (Actual)
Last update posted
Sep 30, 2020

2007 – 2009

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Arizona Clinical Research Center Tucson Arizona 85715 —
University of Southern California - Norris Comprehensive Cancer Center Los Angeles California 90033 —
California Pacific Medical Center Research Institute San Francisco California 94115 —
Yale University New Haven Connecticut 06520 —
Georgetown University, Lombardi Comprehensive Cancer Center Washington D.C. District of Columbia 20007 —
University of Florida - Shands Cancer Center Gainesville Florida 32610 —
Emory University - Winship Cancer Institute Atlanta Georgia 30322 —
Joliet Oncology and Hematology Associates Joliet Illinois 60435 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
Columbia University New York New York 10032 —
Hematology Oncology Associates of Rockland Nyack New York 10960 —
Cleveland Clinic - Taussig Cancer Center Cleveland Ohio 44195 —
Chattanooga Oncology and Hematology Associates Chattanooga Tennessee 37404 —
University of Tennessee Medical Center Knoxville Tennessee 37920 —
Sarah Cannon Research Institute -Tennessee Oncology Nashville Tennessee 37203 —
Virginia Cancer institute Richmond Virginia 23230 —

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 NCT00493441, 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 30, 2020 · Synced Oct 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00493441 live on ClinicalTrials.gov.

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