drugset / Trial / NCT00056654

Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prostate Cancer

NCT00056654

Completed 164 enrolled Abbott
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary purpose of the study is to determine if a new sustained-release 45 mg (depot) formulation of leuprolide acetate will reduce serum testosterone levels to and maintain them at medically castrate levels in subjects with prostatic adenocarcinoma.

Timeline

Start
2003-03
Primary completion
2004-07
Completion
2004-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 45 mg Intramuscular

Indications