Trials / Completed
CompletedNCT00034918
This Study is to Assess the Efficacy and Safety of ZD6474 in Subjects With Metastatic Breast Cancer
An Open-label, Multicenter Phase II Study to Assess the Response of Subjects With Metastatic Breast Cancer Previously Treated With Anthracycline and Taxane Therapy With or Without Capecitabine to ZD6474 (100-mg or 300-mg Daily Oral Dose).
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 44 (planned)
- Sponsor
- Genzyme, a Sanofi Company · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the efficacy of ZD6474 in patients with metastatic breast cancer at 2 dose levels.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ZD6474 |
Timeline
- Start date
- 2002-05-01
- Completion
- 2003-11-01
- First posted
- 2002-05-03
- Last updated
- 2016-08-24
Locations
2 sites across 2 countries: United States, Spain
Source: ClinicalTrials.gov record NCT00034918. Inclusion in this directory is not an endorsement.