Skip to main content
Clinical Trials/NCT01451580
NCT01451580UnknownPhase 2

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

TTY Biopharm1 site in 1 country47 target enrollmentStarted: September 1, 2005Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 2
Sponsor
Enrollment
47
Locations
1

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Masking
None

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • histologically proved breast cancer with metastatic disease

Exclusion Criteria

  • life expectancy less than 3 months.

Investigators

Sponsor
TTY Biopharm
Sponsor Class
Industry

Study Sites (1)

Loading locations...

Similar Trials

Lipo-dox and Cyclophosphamide... | Clinical Trial