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Completed Phase 2 Interventional

The Safety and Efficacy of Ozarelix to Treat Men With Lower Urinary Tract Symptoms Due to Enlargement of the Prostate

ClinicalTrials.gov ID: NCT00427219

Public ClinicalTrials.gov record NCT00427219. 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 22, 2026, 9:39 AM EDT

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

Official title

A Randomized, Double-Blind, Placebo-Controlled Trial of the Safety and Efficacy of Ozarelix, in Patients With Lower Urinary Tract Symptoms(LUTS) Due to Benign Prostatic Hypertrophy (BPH)

Brief summary

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

This study is to compare the efficacy and safety of ozarelix 15 mg given intramuscular (IM) 2 weeks apart on the improvement of symptoms and the duration of improvement for up to 6 months in men with Benign Prostatic Hypertrophy (BPH) who are over 50 years of age.

Study identification

NCT ID
NCT00427219
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Spectrum Pharmaceuticals, Inc
Industry
Enrollment
74 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 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
Jan 23, 2007 (Actual)
Primary completion
Feb 27, 2008 (Actual)
Completion
Feb 27, 2008 (Actual)
Last update posted
Oct 15, 2021

2007 – 2008

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Donald Gleason, MD Tucson Arizona 85712 —
Jay Young, MD Laguna Hills California 92653 —
Alexander Gershman, MD Los Angeles California 90048 —
Stephen Auerbach, MD Newport Beach California 92660 —
Eugene Dula, MD Tarzana California 91356 —
Joel Kaufman, MD Aurora Colorado 80012 —
Ira Klimberg, MD Ocala Florida 34474 —
Joseph Williams, MD Meridian Idaho 83642 —
Christopher Steidle, MD Fort Wayne Indiana 46825 —
Steven Bigg, MD St Louis Missouri 63136 —
Jed Kaminetsky, MD New York New York 10016 —
William Fitch, MD San Antonio Texas 78229 —
Gregg Eure, MD Virginia Beach Virginia 23454 —

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 NCT00427219, 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 Oct 15, 2021 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00427219 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →