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Completed Phase 2 Interventional

Irinotecan in Patients With Advanced Metastatic Breast Cancer Who Have Experienced Failure of an Anthracycline, a Taxane, and Capecitabine

ClinicalTrials.gov ID: NCT00072852

Public ClinicalTrials.gov record NCT00072852. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 8:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Trial of Irinotecan in Patients With Advanced Metastatic Breast Cancer Who Have Experienced Failure of an Anthracycline, a Taxane, and Capecitabine

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this phase II, randomized, open-label clinical trial is to study 2 schedules of single-agent Irinotecan in women with metastatic breast cancer who have experienced failure of prior therapy with an anthracycline, a taxane, and capecitabine. Patients will receive Irinotecan capsules either once each day for 5 days, or once a day for 14 days in 3 week cycles.

Study identification

NCT ID
NCT00072852
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
134 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2003 (Type not available)
Primary completion
May 2007 (Actual)
Completion
May 2007 (Actual)
Last update posted
Oct 16, 2008

2003 – 2007

United States locations

U.S. sites
57
U.S. states
20
U.S. cities
42
Facility City State ZIP Site status
Pfizer Investigational Site Mobile Alabama 36608 —
Pfizer Investigational Site Anchorage Alaska 99508 —
Pfizer Investigational Site Lewistown Idaho 83501 —
Pfizer Investigational Site Alton Illinois 62002 —
Pfizer Investigational Site Indianapolis Indiana 46227 —
Pfizer Investigational Site Overland Park Kansas 66210 —
Pfizer Investigational Site Chalmette Louisiana 70043 —
Pfizer Investigational Site Covington Louisiana 70433 —
Pfizer Investigational Site Mandeville Louisiana 70448 —
Pfizer Investigational Site Metairie Louisiana 70002 —
Pfizer Investigational Site Metairie Louisiana 70006 —
Pfizer Investigational Site New Orleans Louisiana 70115 —
Pfizer Investigational Site Boston Massachusetts 02114 —
Pfizer Investigational Site Boston Massachusetts 02115 —
Pfizer Investigational Site Boston Massachusetts 02130 —
Pfizer Investigational Site Detroit Michigan 48201 —
Pfizer Investigational Site Southaven Mississippi 38671 —
Pfizer Investigational Site Kansas City Missouri 64111 —
Pfizer Investigational Site St Louis Missouri 63136 —
Pfizer Investigational Site St Louis Missouri 63141 —
Pfizer Investigational Site Washington Missouri 63090 —
Pfizer Investigational Site New Brunswick New Jersey 08901-2601 —
Pfizer Investigational Site New Brunswick New Jersey 08903 —
Pfizer Investigational Site New York New York 10021 —
Pfizer Investigational Site Stony Brook New York 11794 —
Pfizer Investigational Site Kettering Ohio 45409 —
Pfizer Investigational Site Oklahoma City Oklahoma 73120 —
Pfizer Investigational Site Greenville South Carolina 29615 —
Pfizer Investigational Site Covington Tennessee 38019 —
Pfizer Investigational Site Franklin Tennessee 37067 —
Pfizer Investigational Site Gallatin Tennessee 37066 —
Pfizer Investigational Site Hermitage Tennessee 37076 —
Pfizer Investigational Site Lebanon Tennessee 37087 —
Pfizer Investigational Site Memphis Tennessee 38120 —
Pfizer Investigational Site Murfreesboro Tennessee 37130 —
Pfizer Investigational Site Nashville Tennessee 37203 —
Pfizer Investigational Site Nashville Tennessee 37205 —
Pfizer Investigational Site Nashville Tennessee 37207 —
Pfizer Investigational Site Nashville Tennessee 37211 —
Pfizer Investigational Site Dallas Texas 75204 —
Pfizer Investigational Site Dallas Texas 75230-2510 —
Pfizer Investigational Site Dallas Texas 75231 —
Pfizer Investigational Site Dallas Texas 75246 —
Pfizer Investigational Site Fort Worth Texas 76104 —
Pfizer Investigational Site Plano Texas 75075-7787 —
Pfizer Investigational Site Tyler Texas 75702 —
Pfizer Investigational Site Federal Way Washington 98003 —
Pfizer Investigational Site Lakewood Washington 98499 —
Pfizer Investigational Site Seattle Washington 98104-2499 —
Pfizer Investigational Site Seattle Washington 98104 —
Pfizer Investigational Site Seattle Washington 98109-1023 —
Pfizer Investigational Site Seattle Washington 98122 —
Pfizer Investigational Site Seattle Washington 98195 —
Pfizer Investigational Site Tacoma Washington 98405 —
Pfizer Investigational Site Vancouver Washington 98684 —
Pfizer Investigational Site Yakima Washington 98902 —
Pfizer Investigational Site Milwaukee Wisconsin 53215 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00072852, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 16, 2008 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00072852 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →