A Trial of Doxil and Multiday Vinorelbine in Patients With Metastatic Breast Cancer
Part of paid clinical trials in Columbus, Ohio.
- Sponsor
- Hematology Oncology Consultants
- Study ID
- NCT00159094
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Doxil and Vinorelbine — DRUG
Study Details
This is a phase II trial of Doxil on day 1 and vinorelbine on days 1 and 2 in women with metastatic breast cancer. Administered every 28 days. A study to assess the safety and efficacy of Doxil and vinorelbine in metastatic breast cancer.
Key Dates
- Start date
- Oct 31, 2003
- Status verified
- Sep 2005
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Primary Outcome Measure
Response rate
Central Contacts
- Leslie R Laufman, MD614-846-0044
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Hematology Oncology Consultants, Inc | Columbus | Ohio | 43235 | Leslie R Laufman, MD (PRINCIPAL_INVESTIGATOR) Harris Spiridonidis, MD (SUB_INVESTIGATOR) Sanjay Yadav, MD (SUB_INVESTIGATOR) |
| Hematology Oncology Consultants, Inc | Newark | Ohio | 43055 | Leslie R Laufman, MD (PRINCIPAL_INVESTIGATOR) Harris Spiridonidis, MD (SUB_INVESTIGATOR) Sanjay Yadav, MD (SUB_INVESTIGATOR) |
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