drugset / Trial / NCT01511874

Efficacy and Safety Study of ELIGARD 22.5mg With Prostate Cancer

NCT01511874

Phase 4 Completed 42 enrolled HanAll BioPharma Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate efficacy and safety of ELIGARD 22.5mg in the treatment of subjects with prostate cancer.

Timeline

Start
2011-01
Primary completion
2013-05
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 22.5 mg Subcutaneous

Indications