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Completed Phase 2 Interventional

Assessment of Onset, Safety & Toleration of UK-369,003 in Male Erectile Dysfunction

ClinicalTrials.gov ID: NCT00141349

Public ClinicalTrials.gov record NCT00141349. 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 Jul 21, 2026, 7:04 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 Double-Blind, Placebo Controlled, Parallel Group, Multicenter Study to Assess the Time to Onset, Safety, and Toleration of Differing Doses and Combinations of Immediate Release and Modified Release Formulations of UK369,003 in Adult Male Subject With Erectile Dysfunction

Study identification

NCT ID
NCT00141349
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
300 participants

Conditions and interventions

Conditions

Interventions

  • UK-369,003 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
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 31, 2005
Primary completion
Not listed
Completion
Jul 31, 2005
Last update posted
Jul 24, 2006

2005

United States locations

U.S. sites
39
U.S. states
17
U.S. cities
33
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35205
Pfizer Investigational Site Birmingham Alabama 35209-5603
Pfizer Investigational Site Birmingham Alabama 35215
Pfizer Investigational Site Mesa Arizona 85201
Pfizer Investigational Site Mesa Arizona 85206
Pfizer Investigational Site Mesa Arizona 85213
Pfizer Investigational Site Tempe Arizona 85282
Pfizer Investigational Site Beverly Hills California 90212
Pfizer Investigational Site San Bernardino California 92404
Pfizer Investigational Site Torrance California 90505
Pfizer Investigational Site Waterbury Connecticut 06708
Pfizer Investigational Site Aventura Florida 33180
Pfizer Investigational Site Pembroke Pines Florida 33028
Pfizer Investigational Site St. Petersburg Florida 33709
Pfizer Investigational Site West Palm Beach Florida 33407
Pfizer Investigational Site Evansville Indiana 47714
Pfizer Investigational Site Fort Wayne Indiana 46825
Pfizer Investigational Site Jeffersonville Indiana 47130
Pfizer Investigational Site Metairie Louisiana 70002
Pfizer Investigational Site Metairie Louisiana 70006
Pfizer Investigational Site Milford Massachusetts 01757
Pfizer Investigational Site Kansas City Missouri 64114
Pfizer Investigational Site New Brunswick New Jersey 08903
Pfizer Investigational Site Albany New York 12206
Pfizer Investigational Site Endwell New York 13760
Pfizer Investigational Site New York New York 10016
Pfizer Investigational Site Raleigh North Carolina 27609-7216
Pfizer Investigational Site Raleigh North Carolina 27609
Pfizer Investigational Site Winston-Salem North Carolina 27103
Pfizer Investigational Site Beachwood Ohio 44122-5402
Pfizer Investigational Site Cincinnati Ohio 45212
Pfizer Investigational Site Cleveland Ohio 44122
Pfizer Investigational Site Bryan Texas 77802
Pfizer Investigational Site Sugar Land Texas 77478
Pfizer Investigational Site Salt Lake City Utah 84109
Pfizer Investigational Site West Jordan Utah 84088
Pfizer Investigational Site Norfolk Virginia 23502
Pfizer Investigational Site Richmond Virginia 23294
Pfizer Investigational Site Milwaukee Wisconsin 53209

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 NCT00141349, 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 Jul 24, 2006 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00141349 live on ClinicalTrials.gov.

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