Breast Cancer Clinical Trial

AZD2171 in Addition to Fulvestrant in Patients With Advanced Breast Cancer.

Summary

The purpose of this study is to determine whether AZD2171 can effectively improve time to tumour progression when added to fulvestrant in patients with advanced hormone sensitive breast cancer who progressed on prior hormonal therapy.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Written informed consent
Females with histological/cytological confirmation of hormone sensitive breast cancer with evidence of metastatic disease
One or more evaluable lesions

Exclusion Criteria:

Prior hormonal therapy with fulvestrant
More than one course of prior systemic cytotoxic chemotherapy for metastatic breast cancer
Prior biologic therapy for ABC including Anti-VEGF agents
Radiation therapy within 4 weeks prior to provision of consent

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

75

Study ID:

NCT00454805

Recruitment Status:

Completed

Sponsor:

AstraZeneca

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There is 1 Location for this study

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Research Site
Burbank California, , United States
Research Site
Los Angeles California, , United States
Research Site
Palm Springs California, , United States
Research Site
Boca Raton Florida, , United States
Research Site
Honolulu Hawaii, , United States
Research Site
New York New York, , United States
Research Site
Fitzroy , , Australia
Research Site
Parkville , , Australia
Research Site
Perth , , Australia
Research Site
Waratah , , Australia
Research Site
Belo Horizonte , , Brazil
Research Site
Curitiba , , Brazil
Research Site
Fortaleza , , Brazil
Research Site
Porto Alegre , , Brazil
Research Site
Santro Andre , , Brazil
Research Site
São Paulo , , Brazil

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

75

Study ID:

NCT00454805

Recruitment Status:

Completed

Sponsor:


AstraZeneca

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