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Electronic Study for Anastrozole Pharmacovigilance Evaluation

Electronic Study for Anastrozole Pharmacovigilance Evaluation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00558168
Acronym
E-SAFE
Enrollment
1850
Registered
2007-11-14
Start date
2004-01-31
Completion date
2008-07-31
Last updated
2008-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early Breast Cancer

Keywords

Anastrazole, safety, early breast cancer

Brief summary

Collecting information regarding adverse events from patients on treatment with anastrazole with early stage breast cancer

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Post-menopausal Early Invasive Breast Cancer Patients who are under anastrazole treatment, who have normal renal and hepatic functions.

Exclusion criteria

* Metastatic breast cancer patients, previous hormonal therapy, other malignancies.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026