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Clinical Trials/NL-OMON29407
NL-OMON29407
Completed
Not Applicable

Three arm randomized parallel phase II/III study evaluating the efficacy and safety of the combinations Epirubicin and Taxotere (ET), Taxotere and Navelbine (TN) and Navelbine and Epirubicin (EN) as first line therapy in patients with metastatic breast cancer.

VU medical center.0 sites111 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Metastic breast cancer.
Sponsor
VU medical center.
Enrollment
111
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

/A

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
VU medical center.

Eligibility Criteria

Inclusion Criteria

  • 1\. Histologically proven breast cancer at first diagnosis. At study entry histological or cytological proof of metastasis is required in case of a single metastatic target lesion.
  • Female metastatic breast cancer patients
  • Measurable disease or evaluable disease (bone metastases only allowed).

Exclusion Criteria

  • 1\. Prior chemotherapy for metastatic disease.
  • 2\. Locally advanced inoperable breast cancer (Stage III B) as only manifestation of the disease.

Outcomes

Primary Outcomes

Not specified

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