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Terminated No phase listed Observational

A Correlative Study for Predicting Response and Toxicity in Patients Receiving Chemotherapy for Breast Cancer

ClinicalTrials.gov ID: NCT00235235

Public ClinicalTrials.gov record NCT00235235. 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 Sep 11, 2026, 2:04 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

Predicting Response and Toxicity in Patients Receiving Chemotherapy for Breast Cancer: A Multicenter Genomic, Proteomic and Pharmacogenomic Correlative Study: Hoosier Oncology Group COE-01

Brief summary

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

The proposed trial provides a unique opportunity in that it combines genomic, proteomic, and pharmacogenomic assessments in patients receiving the most commonly used chemotherapies for advanced breast cancer. To date no other trial has analyzed gene and protein expression at the same time points in the same patient, combined with clinical outcome. Similar to previous attempts to predict response based on expression of a single gene or protein, the researchers expect that neither genomic or proteomic profiling alone will be sufficient to optimize therapy. Rather, the researchers expect an iterative process that combines information gleaned from both platforms, modified to avoid toxicity based on pharmacogenomics.

Study identification

NCT ID
NCT00235235
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Enrollment
80 participants

Conditions and interventions

Conditions

Interventions

Procedure · 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
Aug 31, 2005
Primary completion
Nov 30, 2010
Completion
Nov 30, 2010
Last update posted
Dec 8, 2015

2005 – 2010

United States locations

U.S. sites
10
U.S. states
2
U.S. cities
7
Facility City State ZIP Site status
Cancer Care Center of Southern Indiana Bloomington Indiana 47403
Fort Wayne Oncology & Hematology, Inc Fort Wayne Indiana 46815
Center for Cancer Care at Goshen Health System Goshen Indiana 46527
Indiana University Cancer Center Indianapolis Indiana 46202
Mary Lou Mayer, M.D. Indianapolis Indiana 46227
Community Regional Cancer Center Indianapolis Indiana 46256
Arnett Cancer Care Lafayette Indiana 47904
Horizon Oncology Center Lafayette Indiana 47905
Northern Indiana Cancer Research Consortium South Bend Indiana 46601
Baylor College of Medicine - Methodist Breast Center Houston Texas 77030

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00235235, 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 Dec 8, 2015 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00235235 live on ClinicalTrials.gov.

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