drugset / Trial / NCT01073865

Study to Compare Zoladex™ 10.8 mg With Zoladex 3.6 mg in Pre-menopausal Women With Breast Cancer

NCT01073865 ↗

Phase 3 Completed 222 enrolled AstraZeneca
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

EvaluationDrugModalityDoseRoute
Subject ZD9393 Unknown 3.6 mg Subcutaneous
Subject ZD9393 Unknown 10.8 mg Subcutaneous

Indications