drugset / Trial / NCT00630799

Efficacy and Safety Study of a New Leuprolide Acetate 17 mg Depot to Treat Prostate Cancer Patients

NCT00630799

Phase 3 Terminated 20 enrolled GP-Pharm
Non-randomizedSingle-groupOpen-labelSupportive care

Summary

This is a multi-center, open-label study of 2 doses of leuprolide acetate 17 mg depot, administered three months apart, in subjects with prostate cancer who might benefit from medical androgen deprivation therapy

Timeline

Start
2008-05
Primary completion
2009-04
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 17 mg Intramuscular

Indications