Breast Cancer Clinical Trial

Fulvestrant (FASLODEXâ„¢) as a Treatment in Postmenopausal Women With Estrogen Receptor Positive Breast Cancer

Summary

The purpose of this study is to evaluate fulvestrant in the preliminary stage of breast cancer treatment and assess the relationship between dose, exposure, degree of reduction in tumor markers, and efficacy in postmenopausal women with estrogen receptor positive disease.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Postmenopausal women defined as women who have stopped having menstrual periods
Written informed consent to participate in the trial
Biopsy confirmation of invasive breast cancer
Evidence of hormone sensitivity
Willingness to undergo biopsies

Exclusion Criteria:

Any previous treatment for breast cancer
Unwillingness to stop taking any drug known to affect sex hormonal status or a patient in which it would be inappropriate to stop.
Any severe concurrent condition that would preclude surgery or that would jeopardize compliance with the study, e.g., uncontrolled cardiac disease or uncontrolled diabetes mellitus
The presence of more than one primary tumor
History of hypersensitivity to castor oil
History of known bleeding disorders

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

179

Study ID:

NCT00093002

Recruitment Status:

Completed

Sponsor:

AstraZeneca

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There is 1 Location for this study

See Locations Near You

Research Site
Little Rock Arkansas, , United States
Research Site
Boston Massachusetts, , United States
Research Site
Winchester Massachusetts, , United States
Research Site
Albuquerque New Mexico, , United States
Research Site
Hershey Pennsylvania, , United States
Research Site
Nashville Tennessee, , United States
Research Site
Laredo Texas, , United States
Research Site
Innsbruck , , Austria
Research Site
Salzburg , , Austria
Research Site
Vienna , , Austria
Research Site
Wien , , Austria
Research Site
Barretos , , Brazil
Research Site
Florianopolis , , Brazil
Research Site
Goiamia , , Brazil
Research Site
Porto Alegre , , Brazil
Research Site
Rio de Janeiro , , Brazil
Research Site
Santo Andre , , Brazil
Research Site
Sao Paulo , , Brazil
Research Site
Berlin , , Germany
Research Site
Hannover , , Germany
Research Site
Magdeburg , , Germany
Research Site
Munchen , , Germany
Research Site
Rostock , , Germany
Research Site
Bangalore , , India
Research Site
Hyderabaad , , India
Research Site
New Delhi , , India
Research Site
Pune , , India
Research Site
Trivandrum , , India
Research Site
Birmingham , , United Kingdom
Research Site
Bournemouth , , United Kingdom
Research Site
Dundee , , United Kingdom
Research Site
Edinburgh , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

179

Study ID:

NCT00093002

Recruitment Status:

Completed

Sponsor:


AstraZeneca

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider