Status:

COMPLETED

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

Lead Sponsor:

AstraZeneca

Conditions:

Advanced Breast Cancer

Eligibility:

FEMALE

18-130 years

Phase:

PHASE2

Brief 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 pro...

Eligibility Criteria

Inclusion

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

Exclusion

  • 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

Key Trial Info

Start Date :

March 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2016

Estimated Enrollment :

75 Patients enrolled

Trial Details

Trial ID

NCT00454805

Start Date

March 1 2007

End Date

April 1 2016

Last Update

August 3 2016

Active Locations (16)

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Page 1 of 4 (16 locations)

1

Research Site

Burbank, California, United States

2

Research Site

Los Angeles, California, United States

3

Research Site

Palm Springs, California, United States

4

Research Site

Boca Raton, Florida, United States

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