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Sponsors and Collaborators: |
Dana-Farber Cancer Institute Brigham and Women's Hospital Massachusetts General Hospital |
Information provided by: | Dana-Farber Cancer Institute |
ClinicalTrials.gov Identifier: | NCT00153907 |
The purpose of this study is to find the highest dose of capecitabine and oral navelbine that can be given without causing severe side effects, and to determine the safety, tolerability, and effects (good and bad) of capecitabine given with oral navelbine to patients with advanced breast cancer.
Condition | Intervention | Phase |
Breast Cancer |
Drug: Navelbine Drug: Capecitabine |
Phase I Phase II |
Genetics Home Reference related topics: | breast cancer |
MedlinePlus related topics: | Breast Cancer Cancer |
ChemIDplus related topics: | Vinorelbine Vinorelbine tartrate Capecitabine |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Single Group Assignment, Safety/Efficacy Study |
Official Title: | A Phase I Study of Oral Navelbine and Capecitabine in the Treatment of Metastatic Breast Cancer |
Enrollment: | 40 |
Study Start Date: | March 2002 |
Estimated Study Completion Date: | August 2008 |
Primary Completion Date: | August 2004 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Massachusetts | |||||
Dana-Farber Cancer Institute | |||||
Boston, Massachusetts, United States, 02115 | |||||
Massachusetts General Hospital | |||||
Boston, Massachusetts, United States, 02114 |
Dana-Farber Cancer Institute |
Brigham and Women's Hospital |
Massachusetts General Hospital |
Principal Investigator: | Craig A. Bunnell, MD | Dana-Farber Cancer Institute |
Responsible Party: | Dana-Farber Cancer Institute ( Craig A. Bunnell, MD ) |
Study ID Numbers: | 01-217 |
First Received: | September 8, 2005 |
Last Updated: | December 22, 2007 |
ClinicalTrials.gov Identifier: | NCT00153907 |
Health Authority: | United States: Institutional Review Board |
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