drugset / Trial / NCT03035032

A Study of ELIGARD® in Hormone-dependent Prostate Cancer Patients

NCT03035032

Phase 4 Completed 107 enrolled Astellas Pharma Inc
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study was to evaluate the safety profile of ELIGARD® in ethnic Asian prostate cancer patients.

Timeline

Start
2017-06-23
Primary completion
2019-11-19
Completion
2019-11-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 22.5 mg Subcutaneous

Indications