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NCT00059865 · ClinicalTrials.gov registry record · Phase 1

Gemcitabine Plus Pemetrexed Disodium in Treating Patients With Unresectable or Metastatic Biliary Tract or Gallbladder Cancer

A Phase 1 study, sponsored by Alliance for Clinical Trials in Oncology.

Completed
Registry status
Phase 1
Development phase
68
Enrollment target

NCT00059865: Completed Phase 1 study, sponsored by Alliance for Clinical Trials in Oncology.

NCT00059865 is a Phase 1 study that has completed, run by Alliance for Clinical Trials in Oncology. The registered enrollment target is 68 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00059865, a Phase 1 study, has completed, sponsored by Alliance for Clinical Trials in Oncology.

COMPLETED
Registry status
Phase 1
Development phase
68 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy such as gemcitabine work in different ways to stop tumor cells from dividing so they stop growing or die. Pemetrexed disodium may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth. Combining gemcitabine with pemetrexed disodium may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of gemcitabine when given together with pemetrexed disodium to see how well it works in treating patients with unresectable or metastatic biliary tract or gallbladder cancer.

Interventions

  • DRUG gemcitabine hydrochloride
  • DRUG pemetrexed disodium

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2004-01
Est. Completion 2008-02
Phase Phase 1

What the finished NCT00059865 record still lists

NCT00059865 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% higher).

The record links to 0 conditions, and to 2 interventions - of which gemcitabine hydrochloride is the first listed.

NCT00059865 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00059865 about?

NCT00059865 is a clinical study titled "Gemcitabine Plus Pemetrexed Disodium in Treating Patients With Unresectable or Metastatic Biliary Tract or Gallbladder Cancer". RATIONALE: Drugs used in chemotherapy such as gemcitabine work in different ways to stop tumor cells from dividing so they stop growing or die. Pemetrexed disodium may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth. Combining gemcitabine with pemetrexed disodi...

What is the current status of trial NCT00059865?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 68 participants. The study started on 2004-01. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00059865?

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

Who is sponsoring clinical trial NCT00059865?

This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 446 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00059865's enrollment target sits among peer trials

68 776th of 2000 higher than 1,219 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00059865, the US trial registry maintained by the National Library of Medicine. NCT00059865 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.