Study of Etoposide in Breast Cancer Patients
Completed
Conditions studied: Breast Cancer
In brief
This study will examine how the body handles etoposide, a drug used to treat breast cancer. The knowledge gained may lead to more effective use of the drug with fewer side effects in the future. Breast cancer patients who are receiving etoposide as part of their treatment may participate in this study. Patients will have 18 blood samples (about a teaspoon or less each) drawn over a 72-hour period during and after their infusion of etoposide. The initial blood samples cannot be taken from the same intravenous line (small tube placed in a vein) used to deliver the etoposide, so a second line may have to be placed temporarily to obtain these samples.
Key facts
- Study ID
- NCT00026949
- Run by
- National Cancer Institute (NCI)
- People needed
- 33
- Starts
- 1999-08-01
- Expected to finish
- 2004-08-01
- Last updated by the study team
- 2008-03-04
Who can join
Age: any. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Age greater than or equal to 18 years.
- Patients with breast cancer who are entered on existing Medicine Branch protocols that include high-dose etoposide.
- Must be able to provide informed consent.
Where it is running
- National Cancer Institute (NCI) — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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