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Clinical Trial Details — Status: Recruiting

Administrative data

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

Study information

Verified date October 2011
Source TTY Biopharm
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Drug:
Lipo-Dox


Locations

Country Name City State
Taiwan CGMH Linko

Sponsors (1)

Lead Sponsor Collaborator
TTY Biopharm

Country where clinical trial is conducted

Taiwan, 

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