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NCT00064051 · ClinicalTrials.gov registry record · Phase 2

3-AP and Gemcitabine in Treating Patients With Unresectable or Metastatic Pancreatic Cancer

A Phase 2 study of Pancreatic Cancer, sponsored by Vion Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
7
Study locations

NCT00064051: Completed Phase 2 study of Pancreatic Cancer, sponsored by Vion Pharmaceuticals.

NCT00064051 is a Phase 2 study of Pancreatic Cancer that has completed, run by Vion Pharmaceuticals. The trial reports 7 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00064051, a Phase 2 study of Pancreatic Cancer, has completed, sponsored by Vion Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
7
Study locations

Study Summary

RATIONALE: Drugs used in chemotherapy such as gemcitabine use different ways to stop tumor cells from dividing so they stop growing or die. 3-AP may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth and may help gemcitabine kill more cancer cells by making them more sensitive to the drug. PURPOSE: This phase II trial is studying how well giving gemcitabine together with 3-AP works in treating patients with unresectable or metastatic pancreatic cancer.

Conditions Studied

Interventions

  • DRUG gemcitabine hydrochloride
  • DRUG triapine

Study Locations (7)

England

  • Christie Hospital N.H.S. Trust - Manchester
  • Royal Marsden NHS Foundation Trust - Surrey - Sutton

Illinois

  • University of Chicago Cancer Research Center - Chicago

Indiana

  • Indiana Oncology Hematology Consultants - Indianapolis

Minnesota

  • University of Minnesota Cancer Center - Minneapolis

Tennessee

  • Sarah Cannon Cancer Center at Centennial Medical Center - Nashville

Other

  • Universitair Ziekenhuis Gent - Ghent

Trial Details

FieldValue
Start Date 2003-01
Est. Completion 2008-08
Phase Phase 2
Vion Pharmaceuticals

19 total trials

What the finished NCT00064051 record still lists

NCT00064051 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 1 condition, with Pancreatic Cancer appearing as the primary indexed condition, and to 2 interventions - of which gemcitabine hydrochloride is the first listed.

NCT00064051 lists 7 locations in 6 states (England, Illinois, Indiana).

Frequently Asked Questions

What is clinical trial NCT00064051 about?

NCT00064051 is a clinical study titled "3-AP and Gemcitabine in Treating Patients With Unresectable or Metastatic Pancreatic Cancer". RATIONALE: Drugs used in chemotherapy such as gemcitabine use different ways to stop tumor cells from dividing so they stop growing or die. 3-AP may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth and may help gemcitabine kill more cancer cells by making them m...

What is the current status of trial NCT00064051?

This trial is currently completed. It is a Phase 2 study. The study started on 2003-01. Estimated completion is 2008-08.

What conditions does trial NCT00064051 study?

This clinical trial studies the following conditions: Pancreatic Cancer.

What interventions are being tested in trial NCT00064051?

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

Who is sponsoring clinical trial NCT00064051?

This trial is sponsored by Vion Pharmaceuticals, which has 19 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00064051 being conducted?

This trial has 7 study locations across Illinois, Indiana, Minnesota, Tennessee, England. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00064051, the US trial registry maintained by the National Library of Medicine. NCT00064051 (unsized enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.