Non-interventional Study to Evaluate Arimidex in Postmenopausal Women With Advanced Breast Cancer
This study has been completed.
Sponsor:
AstraZeneca
Information provided by (Responsible Party):
AstraZeneca
ClinicalTrials.gov Identifier:
NCT00562458
First received: November 21, 2007
Last updated: February 4, 2013
Last verified: February 2013
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Advanced Breast Cancer |
Drug: anastrozole |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | ARIMIDEX Study ( Non-interventional Study to Evaluate Arimidex in Adjuvant Therapy in Partial or Complete Response or Stabilized Disease After First Line Chemotherapy in Postmenopausal Women With Advanced Breast Cancer) |
Resource links provided by NLM:
Genetics Home Reference related topics:
breast cancer
Drug Information available for:
Anastrozole
U.S. FDA Resources
Further study details as provided by AstraZeneca:
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
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.
Criteria
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.
Contacts and Locations
No Contacts or Locations Provided
More Information
No publications provided
| Responsible Party: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT00562458 History of Changes |
| Other Study ID Numbers: | NIS-ARO-HCH-2006/1 |
| Study First Received: | November 21, 2007 |
| Last Updated: | February 4, 2013 |
| Health Authority: | Romania: National Medicines Agency |
Keywords provided by AstraZeneca:
|
Advanced breast cancer Advanced breast cancer in postmenopausal women |
Additional relevant MeSH terms:
|
Breast Neoplasms Neoplasms by Site Neoplasms Breast Diseases Skin Diseases Anastrozole Antineoplastic Agents, Hormonal |
Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Aromatase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 16, 2013