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NCT00619021 · ClinicalTrials.gov registry record · Phase 1

Bronchial Artery Infusion of Gemcitabine in Treating Patients With Recurrent or Progressive Non-Small Cell Lung Cancer

A Phase 1 study, sponsored by Masonic Cancer Center, University of Minnesota.

Terminated
Registry status
Phase 1
Development phase
4
Enrollment target

NCT00619021 is a Phase 1 study that was terminated before completion, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 4 participants.

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The verdict

NCT00619021, a Phase 1 study, was terminated before completion, sponsored by Masonic Cancer Center, University of Minnesota.

TERMINATED
Registry status
Phase 1
Development phase
4 participants
Enrollment target

Study Summary

RATIONALE: Bronchial artery infusion uses a catheter to deliver antitumor substances directly to the lungs. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Giving gemcitabine in different ways may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of gemcitabine given by bronchial artery infusion and to see how well it works in treating patients with recurrent or progressive non-small cell lung cancer.

Interventions

  • DRUG gemcitabine hydrochloride

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2003-01
Est. Completion 2009-01
Phase Phase 1

What the Registry Record Tells You About NCT00619021

The ClinicalTrials.gov registry entry for NCT00619021 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Masonic Cancer Center, University of Minnesota, which has 249 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which gemcitabine hydrochloride is the first listed.

NCT00619021 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00619021 about?

NCT00619021 is a clinical study titled "Bronchial Artery Infusion of Gemcitabine in Treating Patients With Recurrent or Progressive Non-Small Cell Lung Cancer". RATIONALE: Bronchial artery infusion uses a catheter to deliver antitumor substances directly to the lungs. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Giving gemcitabine in different ways may kill more tumor ...

What is the current status of trial NCT00619021?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2003-01. Estimated completion is 2009-01.

What interventions are being tested in trial NCT00619021?

The interventions under investigation include: gemcitabine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00619021?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

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

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.