Parameters of Acceptability, Compliance and Efficacy of Fulvestrant in Post-menopausal Patients With Advance Breast Cancer

NCT ID: NCT00878930

Last Updated: 2011-01-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-04-30

Study Completion Date

2010-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The objectives of this study is to obtain information of Faslodex use in the treatment of breast cancer in the clinical practice in Argentina.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

In Argentina, Faslodex is indicated for treating postmenopausal women with hormone receptor-positive locally advanced or metastatic breast cancer with recurrence during or after adjuvant anti-oestrogen therapy or disease progression during anti-oestrogen treatment. This study will provide information regarding the acceptability and compliance of Argentina patients to Faslodex and will provide information regarding the efficacy of this treatment in local population.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Breast Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Postmenopausal women with hormone receptor-positive locally advanced or metastatic breast cancer with recurrence during or after adjuvant anti-estrogen therapy or disease progression during anti-estrogen treatment, currently receiving Faslodex
* Signature of the informed consent

Exclusion Criteria

* Any contraindication to Faslodex administration
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

AZ Argentina

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Research Site

Bahía Blanca, Buenos Aires, Argentina

Site Status

Research Site

Campana, Buenos Aires, Argentina

Site Status

Research Site

Ciudad de Buenos Aires, Buenos Aires, Argentina

Site Status

Research Site

La Plata, Buenos Aires, Argentina

Site Status

Research Site

Mar del Plata, Buenos Aires, Argentina

Site Status

Research Site

Morón, Buenos Aires, Argentina

Site Status

Research Site

Pergamino, Buenos Aires, Argentina

Site Status

Research Site

San Martín, Buenos Aires, Argentina

Site Status

Research Site

Tandil, Buenos Aires, Argentina

Site Status

Research Site

Vicente López, Buenos Aires, Argentina

Site Status

Research Site

Córdoba, Córdoba Province, Argentina

Site Status

Research Site

Santa Rosa, La Pampa Province, Argentina

Site Status

Research Site

Mendoza, Mendoza Province, Argentina

Site Status

Research Site

Rosario, Santa Fe Province, Argentina

Site Status

Research Site

Río Grande, Tierra del Fuego Province, Argentina

Site Status

Research Site

San Miguel de Tucumán, Tucumán Province, Argentina

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Argentina

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NIS-OAR-FAS-2008/1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Efficacy and Safety of 500mg of Fulvestrant
NCT00585507 ACTIVE_NOT_RECRUITING PHASE2