ClinicalTrials.gov record
Terminated Phase 3 Interventional Results available

Trial In Pediatric Patients With Familial Adenomatous Polyposis (FAP)

ClinicalTrials.gov ID: NCT00585312

Public ClinicalTrials.gov record NCT00585312. 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 May 5, 2026, 7:12 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

A Phase III Placebo-Controlled Trial Of Celecoxib In Genotype Positive Subjects With Familial Adenomatous Polyposis

Study identification

NCT ID
NCT00585312
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Enrollment
106 participants

Conditions and interventions

Interventions

  • Celecoxib Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
10 Years to 17 Years
Sex
All
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
Aug 31, 2006
Primary completion
Sep 30, 2013
Completion
Sep 30, 2013
Last update posted
Feb 20, 2021

2006 – 2013

United States locations

U.S. sites
23
U.S. states
8
U.S. cities
19
Facility City State ZIP Site status
Pfizer Investigational Site Chicago Illinois 60612
Pfizer Investigational Site Ann Arbor Michigan 48109
Pfizer Investigational Site Omaha Nebraska 68114
Pfizer Investigational Site New York New York 10017
Pfizer Investigational Site New York New York 10022
Pfizer Investigational Site New York New York 10065
Pfizer Investigational Site Chagrin Falls Ohio 44136
Pfizer Investigational Site Cincinnati Ohio 45229
Pfizer Investigational Site Cleveland Ohio 44122
Pfizer Investigational Site Cleveland Ohio 44195
Pfizer Investigational Site Elyria Ohio 44035
Pfizer Investigational Site Independence Ohio 44131
Pfizer Investigational Site Lakewood Ohio 44107
Pfizer Investigational Site Lorain Ohio 44053
Pfizer Investigational Site Solon Ohio 44138
Pfizer Investigational Site Strongsville Ohio 44136
Pfizer Investigational Site Westlake Ohio 44145
Pfizer Investigational Site Willoughby Hills Ohio 44094
Pfizer Investigational Site Wooster Ohio 44691
Pfizer Investigational Site Nashville Tennessee 37232
Pfizer Investigational Site Houston Texas 77030-4990
Pfizer Investigational Site Salt Lake City Utah 84112
Pfizer Investigational Site Salt Lake City Utah 84132

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00585312, 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 Feb 20, 2021 · Synced May 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00585312 live on ClinicalTrials.gov.

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