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NCT00091078 · ClinicalTrials.gov registry record · Phase 2

Oblimersen and Imatinib Mesylate in Treating Patients With Advanced Gastrointestinal Stromal Tumors That Cannot Be Removed By Surgery

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Terminated
Registry status
Phase 2
Development phase
96
Enrollment target

NCT00091078: Clinical Trial Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00091078 is a Phase 2 study that was terminated before completion, run by National Cancer Institute (NCI). The registered enrollment target is 96 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00091078, a Phase 2 study, was terminated before completion, sponsored by National Cancer Institute (NCI).

TERMINATED
Registry status
Phase 2
Development phase
96 participants
Enrollment target

Study Summary

Imatinib mesylate may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Oblimersen may help imatinib mesylate kill more tumor cells by making tumor cells more sensitive to the drug. This phase II trial is studying how well giving imatinib mesylate together with oblimersen works in treating patients with advanced gastrointestinal stromal tumor that cannot be removed by surgery.

Primary Outcome

The design method of Thall, Simon and Estey will be used.

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG imatinib mesylate
  • BIOLOGICAL oblimersen sodium

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2005-09
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

Why NCT00091078 stopped before completion

NCT00091078 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 3 interventions - of which laboratory biomarker analysis is the first listed.

NCT00091078 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00091078 about?

NCT00091078 is a clinical study titled "Oblimersen and Imatinib Mesylate in Treating Patients With Advanced Gastrointestinal Stromal Tumors That Cannot Be Removed By Surgery". Imatinib mesylate may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Oblimersen may help imatinib mesylate kill more tumor cells by making tumor cells more sensitive to the drug. This phase II trial is studying how well giving imatinib mesylate together with oblim...

What is the current status of trial NCT00091078?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 96 participants. The study started on 2005-09.

What interventions are being tested in trial NCT00091078?

The interventions under investigation include: laboratory biomarker analysis (OTHER), imatinib mesylate (DRUG), oblimersen sodium (BIOLOGICAL).

Who is sponsoring clinical trial NCT00091078?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00091078's enrollment target sits among peer trials

96 747th of 2000 higher than 1,242 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00091078, the US trial registry maintained by the National Library of Medicine. NCT00091078 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.