Metastatic Breast Cancer Clinical Trial
Official title:
A Phase II Study of Pegylated Liposomal Doxorubicin (Lipo-Dox) Combined With Cyclophosphamide /5-Fluorouracil as Second Line Chemotherapy in the Treatment of Metastatic Breast Cancer
| NCT number | NCT01451580 |
| Other study ID # | LD0411 |
| Secondary ID | |
| Status | Recruiting |
| Phase | Phase 2 |
| First received | October 11, 2011 |
| Last updated | October 12, 2011 |
| Start date | September 2005 |
| Verified date | October 2011 |
| Source | TTY Biopharm |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Taiwan: Department of Health |
| Study type | Interventional |
To determine the overall objective response rate of pegylated liposomal doxorubicin （Lipo-Dox）combined with cyclophosphamide/5-FU as second-line treatment in patients with metastatic breast cancer.
| Status | Recruiting |
| Enrollment | 47 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 20 Years and older |
| Eligibility |
Inclusion Criteria: - histologically proved breast cancer with metastatic disease Exclusion Criteria: - life expectancy less than 3 months. |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label
| Country | Name | City | State |
|---|---|---|---|
| Taiwan | CGMH | Linko |
| Lead Sponsor | Collaborator |
|---|---|
| TTY Biopharm |
Taiwan,
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