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NCT00198159 · ClinicalTrials.gov registry record · Phase 2

A Phase II Study of Iressa in Patients With Chemo Refractory Germ Cell Tumors Expressing EGFR

A Phase 2 study, sponsored by Indiana University.

Terminated
Registry status
Phase 2
Development phase
21
Enrollment target

NCT00198159: Clinical Trial Phase 2 study, sponsored by Indiana University.

NCT00198159 is a Phase 2 study that was terminated before completion, run by Indiana University. The registered enrollment target is 21 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00198159, a Phase 2 study, was terminated before completion, sponsored by Indiana University.

TERMINATED
Registry status
Phase 2
Development phase
21 participants
Enrollment target

Study Summary

This study will evaluate the use of ZD1839 in the treatment of subjects with refractory germ cell tumors. Subjects will take ZD1839 for one year in the absence of excessive toxicity or decision to withdraw.

Interventions

  • DRUG ZD1839 Iressa

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2002-09
Est. Completion 2006-03
Phase Phase 2
Indiana University

890 total trials

Why NCT00198159 stopped before completion

NCT00198159 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 1 intervention - of which ZD1839 Iressa is the first listed.

NCT00198159 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00198159 about?

NCT00198159 is a clinical study titled "A Phase II Study of Iressa in Patients With Chemo Refractory Germ Cell Tumors Expressing EGFR". This study will evaluate the use of ZD1839 in the treatment of subjects with refractory germ cell tumors. Subjects will take ZD1839 for one year in the absence of excessive toxicity or decision to withdraw.

What is the current status of trial NCT00198159?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 21 participants. The study started on 2002-09. Estimated completion is 2006-03.

What interventions are being tested in trial NCT00198159?

The interventions under investigation include: ZD1839 Iressa (DRUG).

Who is sponsoring clinical trial NCT00198159?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00198159's enrollment target sits among peer trials

21 1794th of 2000 higher than 196 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 NCT00198159, the US trial registry maintained by the National Library of Medicine. NCT00198159 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.