Clinical Trials Directory

Trials / Terminated

TerminatedNCT00225056

Phase II Study of Capecitabine and Weekly Docetaxel Followed by Capecitabine Maintenance for Patients With Metastatic Breast Carcinoma

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
43 (planned)
Sponsor
Oncology Specialties, Alabama · Academic / Other
Sex
Female
Age
19 Years – 85 Years
Healthy volunteers

Summary

In this phase II study, we plan to evaluate the efficacy, safety and tolerability of weekly docetaxel and capecitabine on a 21-day cycle followed by maintenance single agent capecitabine for the treatment of metastatic breast cancer, Based on the efficacy and toxicity of the combination regimen dosages previously reviewed; weekly docetaxel 30mg/m2 on days 1 and 8 plus capecitabine 1600mg/m2 (800mg/m2 orally twice daily)on day 1 through 14 of each cycle will be utilized.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxel and capecitabine

Timeline

Start date
2003-10-01
Completion
2006-11-01
First posted
2005-09-23
Last updated
2007-04-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00225056. Inclusion in this directory is not an endorsement.