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Completed Phase 2 Interventional Results available

A Study to Investigate the Safety and Efficacy of CP-690,550 in Patients With Moderate to Severe Crohn's Disease

ClinicalTrials.gov ID: NCT00615199

Public ClinicalTrials.gov record NCT00615199. 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 Sep 26, 2026, 6:35 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, Parallel Group, Multi-Center Study To Investigate The Safety And Efficacy Of CP-690,550 In Subjects With Moderate To Severe Crohn's Disease.

Brief summary

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

This study investigates safety and efficacy of CP-690,550 in adult patients with moderate to severe Crohn's disease. The study hypothesis is that at least one of the dose levels to be tested will be more effective than placebo (inactive drug).

Study identification

NCT ID
NCT00615199
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
139 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Dec 31, 2007
Primary completion
Sep 30, 2009
Completion
Sep 30, 2009
Last update posted
Jan 24, 2013

2008 – 2009

United States locations

U.S. sites
39
U.S. states
19
U.S. cities
31
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35233 —
Pfizer Investigational Site Mobile Alabama 36617 —
Pfizer Investigational Site Boulder Colorado 80304 —
Pfizer Investigational Site Lakewood Colorado 80215 —
Pfizer Investigational Site Wheat Ridge Colorado 80033 —
Pfizer Investigational Site Washington D.C. District of Columbia 20006 —
Pfizer Investigational Site Boca Raton Florida 33428 —
Pfizer Investigational Site Boca Raton Florida 33442 —
Pfizer Investigational Site Boca Raton Florida 33486 —
Pfizer Investigational Site Boca Raton Florida 33496 —
Pfizer Investigational Site Gainesville Florida 32605 —
Pfizer Investigational Site Gainesville Florida 32607 —
Pfizer Investigational Site Jacksonville Florida 32207 —
Pfizer Investigational Site Jacksonville Florida 32256 —
Pfizer Investigational Site St. Petersburg Florida 33709 —
Pfizer Investigational Site Chicago Illinois 60637 —
Pfizer Investigational Site Wichita Kansas 67208 —
Pfizer Investigational Site Louisville Kentucky 40202 —
Pfizer Investigational Site Chevy Chase Maryland 20815 —
Pfizer Investigational Site Towson Maryland 21204 —
Pfizer Investigational Site Troy Michigan 48098 —
Pfizer Investigational Site Rochester Minnesota 55905 —
Pfizer Investigational Site Mexico Missouri 65265 —
Pfizer Investigational Site Great Neck New York 11021 —
Pfizer Investigational Site Charlotte North Carolina 28209 —
Pfizer Investigational Site Charlotte North Carolina 28210 —
Pfizer Investigational Site Charlotte North Carolina 28211 —
Pfizer Investigational Site Salisbury North Carolina 28144 —
Pfizer Investigational Site Dayton Ohio 45415 —
Pfizer Investigational Site Duncansville Pennsylvania 16635 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15243 —
Pfizer Investigational Site Upper Saint Clair Pennsylvania 15241 —
Pfizer Investigational Site Bristol Tennessee 37620 —
Pfizer Investigational Site Kingsport Tennessee 37660 —
Pfizer Investigational Site Nashville Tennessee 37205 —
Pfizer Investigational Site Dallas Texas 75235 —
Pfizer Investigational Site Dallas Texas 75390-8887 —
Pfizer Investigational Site Seattle Washington 98195 —
Pfizer Investigational Site Charleston West Virginia 25304 —

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 33 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00615199, 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 Jan 24, 2013 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00615199 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →