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NCT00059787 · ClinicalTrials.gov registry record · Phase 2

Erlotinib Plus Carboplatin and Paclitaxel in Ovarian Carcinoma

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

Completed
Registry status
Phase 2
Development phase
56
Enrollment target

NCT00059787: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00059787 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 56 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00059787, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
56 participants
Enrollment target

Study Summary

This phase II trial is studying the side effects of giving erlotinib together with carboplatin and paclitaxel and to see how well it works in treating patients with stage III or stage IV ovarian, fallopian tube, or primary peritoneal cancer. Biological therapies such as erlotinib may interfere with the growth of tumor cells and slow the growth of the tumor. Drugs used in chemotherapy such as carboplatin and paclitaxel use different ways to stop tumor cells from dividing so they stop growing or die.

Primary Outcome

Pathologic complete response was defined as having no pathologic or cytologic evidence of disease following surgical reassessment.

Interventions

  • DRUG carboplatin
  • DRUG paclitaxel
  • DRUG erlotinib

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2003-04
Est. Completion 2010-05
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00059787 record still lists

NCT00059787 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% lower).

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

NCT00059787 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00059787 about?

NCT00059787 is a clinical study titled "Erlotinib Plus Carboplatin and Paclitaxel in Ovarian Carcinoma". This phase II trial is studying the side effects of giving erlotinib together with carboplatin and paclitaxel and to see how well it works in treating patients with stage III or stage IV ovarian, fallopian tube, or primary peritoneal cancer. Biological therapies such as erlotinib may interfere with ...

What is the current status of trial NCT00059787?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 56 participants. The study started on 2003-04. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00059787?

The interventions under investigation include: carboplatin (DRUG), paclitaxel (DRUG), erlotinib (DRUG).

Who is sponsoring clinical trial NCT00059787?

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 NCT00059787's enrollment target sits among peer trials

56 1146th of 2000 higher than 848 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 NCT00059787, the US trial registry maintained by the National Library of Medicine. NCT00059787 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.