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NCT00626158 · ClinicalTrials.gov registry record · Phase 1

Gemcitabine and Capecitabine to Treat Patients With Advanced Pancreatic and Biliary Cancers

A Phase 1 study of Pancreatic Cancer and Biliary Cancer, sponsored by University of California, San Francisco.

Completed
Registry status
Phase 1
Development phase
45
Enrollment target
2
Study locations

NCT00626158 is a Phase 1 study of Pancreatic Cancer and Biliary Cancer that has completed, run by University of California, San Francisco. The registered enrollment target is 45 participants, below the 393-participant average among 278 other Pancreatic Cancer trials with a reported enrollment target (89% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT00626158, a Phase 1 study of Pancreatic Cancer and Biliary Cancer, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
Phase 1
Development phase
45 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to find out what effects gemcitabine plus capecitabine has on patients with pancreatic or biliary cancer, and to determine the optimal dose that can be given safely of these two drugs together (called the maximum tolerated dose). Gemcitabine and capecitabine are two chemotherapy drugs used to treat pancreatic and biliary cancer. These two drugs used together are considered an acceptable standard of care for pancreatic and biliary cancers. However, in this study the dose and dosing schedule will be changed, in the hopes that the drugs will have more effect with fewer side effects than when given in the standard way.

Interventions

  • DRUG gemcitabine
  • DRUG capecitabine

Study Locations (2)

California

  • UCSF Helen Diller Family Comprehensive Cancer Center - San Francisco

Utah

  • Huntsman Cancer Center, University of Utah - Salt Lake City

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2008-02
Est. Completion 2010-12
Phase Phase 1

What the Registry Record Tells You About NCT00626158

The ClinicalTrials.gov registry entry for NCT00626158 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 393-participant average among 278 other Pancreatic Cancer trials with a reported enrollment target (89% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pancreatic Cancer appearing as the primary indexed condition, and to 2 interventions - of which gemcitabine is the first listed.

NCT00626158 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Utah.

Frequently Asked Questions

What is clinical trial NCT00626158 about?

NCT00626158 is a clinical study titled "Gemcitabine and Capecitabine to Treat Patients With Advanced Pancreatic and Biliary Cancers". The purpose of this study is to find out what effects gemcitabine plus capecitabine has on patients with pancreatic or biliary cancer, and to determine the optimal dose that can be given safely of these two drugs together (called the maximum tolerated dose). Gemcitabine and capecitabine are two chem...

What is the current status of trial NCT00626158?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 45 participants. The study started on 2008-02. Estimated completion is 2010-12.

What conditions does trial NCT00626158 study?

This clinical trial studies the following conditions: Pancreatic Cancer, Biliary Cancer.

What interventions are being tested in trial NCT00626158?

The interventions under investigation include: gemcitabine (DRUG), capecitabine (DRUG).

Who is sponsoring clinical trial NCT00626158?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00626158 being conducted?

This trial has 2 study locations across California, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.