drugset / Trial / NCT00626431

A Study of Leuprolide to Treat Prostate Cancer

NCT00626431

Phase 3 Completed 310 enrolled Abbott
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To assess the efficacy and safety of 2 new formulations of leuprolide acetate 45 mg 6-month depot, Formulation A or Formulation B, for the treatment of patients with prostate cancer. A formulation will be deemed successful if the percentage of subjects with suppression of testosterone to \<= 50 ng/dL from Week 4 to Week 48 is not less than 87%, (the lower bound of the 2-sided 90% confidence interval), a protocol-specified criterion.

Timeline

Start
2008-02
Primary completion
2009-08
Completion
2009-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 45 mg Intramuscular

Indications