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NCT00051051 · ClinicalTrials.gov registry record · Phase 2

A Phase II Study of CI-1033 in Treating Patients With Metastatic (Stage IV) Breast Cancer

A Phase 2 study, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
168
Enrollment target

NCT00051051: Completed Phase 2 study, sponsored by Pfizer.

NCT00051051 is a Phase 2 study that has completed, run by Pfizer. The registered enrollment target is 168 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (26% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00051051, a Phase 2 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
168 participants
Enrollment target

Study Summary

CI-1033 is an experimental drug that acts as an inhibitor of erbB (EGFR) receptors, which may be involved in tumor growth. The primary objective of this study is to assess the antitumor activity of CI-1033 in patients with metastatic breast cancer. Patients with histologically confirmed metastatic (Stage IV) breast cancer and who have received no more than 2 prior cytotoxic chemotherapy regimens are eligible for this study. CI-1033 is administered orally. Patients are required to have blood tests periodically while receiving treatment and will be closely monitored throughout the study for possible side effects and response to treatment. Patients may not have received any prior treatment with other agents that target erbB receptors, including Herceptin (trastuzumab) or Iressa (gefitinib).

Interventions

  • DRUG CI-1033

Trial Details

FieldValue
Enrollment Target 168 participants
Start Date 2002-12
Est. Completion 2005-05
Phase Phase 2
Pfizer

1,845 total trials

What the finished NCT00051051 record still lists

NCT00051051 is an interventional study that assigns participants to a tested intervention. The registered 168 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (26% higher).

The record links to 0 conditions, and to 1 intervention - of which CI-1033 is the first listed.

NCT00051051 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00051051 about?

NCT00051051 is a clinical study titled "A Phase II Study of CI-1033 in Treating Patients With Metastatic (Stage IV) Breast Cancer". CI-1033 is an experimental drug that acts as an inhibitor of erbB (EGFR) receptors, which may be involved in tumor growth. The primary objective of this study is to assess the antitumor activity of CI-1033 in patients with metastatic breast cancer. Patients with histologically confirmed metastatic (...

What is the current status of trial NCT00051051?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 168 participants. The study started on 2002-12. Estimated completion is 2005-05.

What interventions are being tested in trial NCT00051051?

The interventions under investigation include: CI-1033 (DRUG).

Who is sponsoring clinical trial NCT00051051?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00051051's enrollment target sits among peer trials

168 403rd of 2000 higher than 1,595 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 NCT00051051, the US trial registry maintained by the National Library of Medicine. NCT00051051 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.