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Terminated Phase 2 Interventional Results available

Efficacy, Safety and Tolerability of PF-06687234 as Add-on Therapy to Infliximab in Active UC Subjects Not in Remission.

ClinicalTrials.gov ID: NCT03269695

Public ClinicalTrials.gov record NCT03269695. 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 3, 2026, 9:52 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 2A, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PF-06687234 AS ADD-ON THERAPY TO INFLIXIMAB IN ACTIVE ULCERATIVE COLITIS SUBJECTS WHO ARE NOT IN REMISSION (BUILD UC)

Brief summary

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

The purpose of this study is to determine if PF-06687234 is effective and safe as add-on therapy to infliximab in subjects with active ulcerative colitis who are not in remission.

Study identification

NCT ID
NCT03269695
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
20 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Dec 19, 2017
Primary completion
Jan 6, 2021
Completion
Jan 6, 2021
Last update posted
Dec 27, 2021

2017 – 2021

United States locations

U.S. sites
14
U.S. states
5
U.S. cities
9
Facility City State ZIP Site status
Dothan Surgery Center Dothan Alabama 36301
Gut PC, dba Digestive Health Specialists of the Southeast Dothan Alabama 36305
Emory Investigational Drug Services Atlanta Georgia 30322
Emory University Hospital Atlanta Georgia 30322
Emory University School of Medicine Atlanta Georgia 30322
The Emory Clinic Atlanta Georgia 30322
Chevy Chase Endoscopy Center Chevy Chase Maryland 20815
MGG Group Co., Inc., Chevy Chase Clinical Research Chevy Chase Maryland 20815
Clinical Research Institute of Michigan, LLC Chesterfield Michigan 48047
East Valley Endoscopy Grand Rapids Michigan 49546
Eastside Endoscopy Center Macomb Michigan 48044
Eastside Endoscopy Center Saint Clair Shores Michigan 48041
Gastroenterology Associates of Western Michigan, PLC d.b.a. West Michigan Clinical Research Center Wyoming Michigan 49519
Allegiance Research Specialists Wauwatosa Wisconsin 53226

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03269695, 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 Dec 27, 2021 · Synced Sep 3, 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 NCT03269695 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →