Clinical Trials Directory

Trials / Completed

CompletedNCT00201435

Weekly Taxol Plus Xeloda® vs Taxotere q3wk Plus Xeloda® in the Treatment of Metastatic BC

Weekly Taxol® Plus Xeloda® Versus Taxotere® Every Three Weeks Plus Xeloda® in the Treatment of Metastatic Breast Cancer A Phase II/III Study

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
224 (estimated)
Sponsor
Norwegian Breast Cancer Group · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

We want to compare Taxol given weekly with Taxotere given every 3 week both in comination with Xeloda. We are going to compare time to treatment failure and quality of life.

Detailed description

Open labeled randomized multicentre phase II/III trial. It is intended to include patients who are not usually included into clinical trials because they are not having disease with measurable lesions. In breast cancer the bulk of patients with metastatic disease is presenting with bone metastases which is difficult to evaluate with respect to response. In this study it is one of the main objectives to include this kind of everyday patients that we see in the clinic. Because of this we will be using TTF as the primary endpoint. Skeletal events requiring radiotherapy or major changes in pain medications are defined as treatment failures causing stop in treatment even in the absence of radiological findings. A: weekly Taxol® plus Xeloda® on days 1-14 q 3w B: Taxotere® q 3w plus Xeloda® on days 1-14 q 3w Patients are randomized equally between the two arms. Concomitant therapy: Simultaneous use of bisphosphonates is allowed, if this treatment has been initiated at least four weeks before study entry.

Conditions

Interventions

TypeNameDescription
DRUGPaclitaxel weekly in combination with capecitabine
DRUGDocetaxel every 3 week in combination with capecitabine

Timeline

Start date
2005-03-01
Primary completion
2008-01-01
Completion
2008-05-01
First posted
2005-09-20
Last updated
2008-05-20

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT00201435. Inclusion in this directory is not an endorsement.