Leuprolide Acetate 3.75 mg Depot to Treat Prostate Cancer

NCT00128531 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2007-11-14

No results posted yet for this study

Summary

The purpose of this study is to look at the efficacy and safety of leuprolide acetate in patients with prostate cancer.

Conditions

Interventions

DRUG

leuprolide acetate

Sponsors & Collaborators

  • GP-Pharm

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Completion
2007-11-30

Countries

  • United States
  • Austria
  • Czechia
  • Germany
  • Hungary
  • Italy
  • Slovakia
  • Spain
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00128531 on ClinicalTrials.gov