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
| Type | Name | Description |
|---|---|---|
| DRUG | docetaxel & 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.