drugset / Trial / NCT01073865
Study to Compare Zoladex™ 10.8 mg With Zoladex 3.6 mg in Pre-menopausal Women With Breast Cancer
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to examine the efficacy and safety as well as the characteristics of the female hormone and study medications after administration in pre-menopausal women with estrogen receptor positive advanced breast cancer who were randomised in a 1:1 ratio to either of the two treatment groups; the ZD9393 3.6 mg depot group or ZD9393 10.8 mg depot group, both given in combination with tamoxifen tablets.
Timeline
- Start
- 2010-02-26
- Primary completion
- 2012-09-19
- Completion
- 2017-11-20
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ZD9393 | Unknown | 3.6 mg | Subcutaneous |
| Subject | ZD9393 | Unknown | 10.8 mg | Subcutaneous |