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Completed Phase 2 Interventional

Study Evaluating The Efficacy And Safety Of SBI-087 In Seropositive Subjects With Active Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT01008852

Public ClinicalTrials.gov record NCT01008852. 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 10, 2026, 5:46 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

Randomized, Parallel, Double-Blind, Placebo-Controlled Trial To Evaluate The Efficacy And Safety Of SBI-087 In Seropositive Subjects With Active Rheumatoid Arthritis On A Stable Background Of Methotrexate

Brief summary

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

This study is designed to evaluate the safety and efficacy of a dose and dosage regimen of SBI-087 in seropositive patients with active Rheumatoid Arthritis, who are on a stable dose of methotrexate.

Study identification

NCT ID
NCT01008852
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
210 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
Nov 30, 2009
Primary completion
Aug 31, 2011
Completion
Jun 30, 2013
Last update posted
Dec 2, 2013

2009 – 2013

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Pfizer Investigational Site Paradise Valley Arizona 85253
Pfizer Investigational Site Palm Desert California 92260
Pfizer Investigational Site Santa Monica California 90404
Pfizer Investigational Site Westlake Village California 91361
Pfizer Investigational Site Newark Delaware 19713
Pfizer Investigational Site Miami Florida 33169
Pfizer Investigational Site Palm Harbor Florida 34684
Pfizer Investigational Site Springfield Illinois 62704
Pfizer Investigational Site Worcester Massachusetts 01610
Pfizer Investigational Site Grand Rapids Michigan 49546
Pfizer Investigational Site Albuquerque New Mexico 87102
Pfizer Investigational Site Syracuse New York 13210
Pfizer Investigational Site Minot North Dakota 58701
Pfizer Investigational Site Dayton Ohio 45408
Pfizer Investigational Site Toledo Ohio 43606
Pfizer Investigational Site Tulsa Oklahoma 74135
Pfizer Investigational Site Charleston South Carolina 29406
Pfizer Investigational Site Jackson Tennessee 38305
Pfizer Investigational Site Spokane Washington 99204
Pfizer Investigational Site Clarksburg West Virginia 26301

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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01008852, 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 2, 2013 · Synced Sep 10, 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 NCT01008852 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →