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Non-interventional Study to Evaluate Arimidex in Postmenopausal Women With Advanced Breast Cancer

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Advanced Breast Cancer

Treatments

Drug: anastrozole

Study type

Observational

Funder types

Industry

Identifiers

NCT00562458
NIS-ARO-HCH-2006/1

Details and patient eligibility

About

To evaluate Arimidex 6 month therapy as an adjuvant treatment in postmenopausal patients with advanced breast cancer in whom a partial or complete response or stabilized disease were obtained with first line chemotherapy, by tumoral response assessment.

Enrollment

200 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients to be included in the program are that ones according to the indications specified in the Romanian anastrozole (Arimidex) approved SmPC (attached to the protocol)and who are already treated with anastrozole for at least 1 month before inclusion in this program/non-interventional study.

Exclusion criteria

  • Patients not to be included in the programme: patients who have a known hypersensitivity to anastrozole (Arimidex®) or any of its excipients.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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