Clinical Trials Directory

Trials / Completed

CompletedNCT00198237

Genomic & Proteomic Analysis of Docetaxel & Capecitabine as Primary Chemo for Stage II-III Breast Cancer

Genomic and Proteomic Analysis of Docetaxel and Capecitabine as Primary Chemotherapy for Stage II-III Breast Cancer

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (planned)
Sponsor
Indiana University School of Medicine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to determine the efficacy \& toxicity of combined docetaxel \& capecitabine as primary chemo for subjects w/ stage II-III breast cancer.

Detailed description

The primary objective of this study is to determine the efficacy \& toxicity of combined docetaxel \& capecitabine as primary chemotherapy for subjects with stage II-III breast cancer.Subjects will be randomized into one of two groups: Docetaxel followed by four cycles of docetaxel \& capecitabine vs. capecitabine followed by four cycles of docetaxel and capecitabine.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxel & capecitabine

Timeline

Start date
2003-03-01
Completion
2005-12-01
First posted
2005-09-20
Last updated
2014-06-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00198237. Inclusion in this directory is not an endorsement.

Genomic & Proteomic Analysis of Docetaxel & Capecitabine as Primary Chemo for Stage II-III Breast Cancer (NCT00198237) · Clinical Trials Directory