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Terminated Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT00630799

Public ClinicalTrials.gov record NCT00630799. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 9:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Efficacy and Safety of a New Leuprolide Acetate 17 mg Depot Formulation, GP-Pharm S.A., When Given as Palliative Treatment to Prostate Cancer Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT00630799
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
GP-Pharm
Industry
Enrollment
20 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2008 (Type not available)
Primary completion
Apr 2009 (Actual)
Completion
Jul 2009 (Actual)
Last update posted
Sep 9, 2010

2008 – 2009

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Advanced Research Institute New Port Richey Florida 34655 —
Lawrenceville Urology Lawrenceville New Jersey 08648 —
Hudson Valley Urology Poughkeepsie New York 12601 —
Piedmont Medical Research Winston-Salem North Carolina 27103 —
Center for Urologic Care Bryn Mawr Pennsylvania 19010 —
Carolina Urologic Research Center Myrtle Beach South Carolina 29572 —
Urology Associates Nashville Tennessee 37209 —
Urology San Antonio Research, PA San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00630799, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 9, 2010 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00630799 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →