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Terminated Phase 2 Interventional Results available

Study Evaluating Bosutinib-Exemestane Combination Vs Exemestane Alone in Post Menopausal Women With Breast Cancer

ClinicalTrials.gov ID: NCT00793546

Public ClinicalTrials.gov record NCT00793546. 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 Jun 25, 2026, 5:31 AM EDT

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

Official title

A Phase 2, Randomized, Open-Label Study Of Bosutinib Administered In Combination With Exemestane Versus Exemestane Alone As Second Line Therapy In Postmenopausal Women With Locally Advanced Or Metastatic ER+/PgR+/ErbB2- Breast Cancer

Study identification

NCT ID
NCT00793546
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
42 participants

Conditions and interventions

Interventions

  • Bosutinib Drug
  • Exemestane Drug

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
Jan 31, 2009
Primary completion
May 31, 2010
Completion
May 31, 2010
Last update posted
Nov 4, 2012

2009 – 2010

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Pfizer Investigational Site Lake Worth Florida 33461
Pfizer Investigational Site Joliet Illinois 60435
Pfizer Investigational Site Boston Massachusetts 02114
Pfizer Investigational Site Boston Massachusetts 02115
Pfizer Investigational Site Detroit Michigan 84202
Pfizer Investigational Site New Brunswick New Jersey 08901
Pfizer Investigational Site New York New York 10032
Pfizer Investigational Site Bethlehem Pennsylvania 18015
Pfizer Investigational Site Philadelphia Pennsylvania 19104-4283
Pfizer Investigational Site Philadelphia Pennsylvania 19104
Pfizer Investigational Site Seattle Washington 98104

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00793546, 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 Nov 4, 2012 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00793546 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →