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Completed Phase 2 Interventional Results available

Safety and Efficacy of Pf-06650833 In Subjects With Rheumatoid Arthritis, With An Inadequate Response To Methotrexate

ClinicalTrials.gov ID: NCT02996500

Public ClinicalTrials.gov record NCT02996500. 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 Oct 20, 2026, 8:53 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 12 WEEK RANDOMIZED, DOUBLE-BLIND, DOUBLE DUMMY, PARALLEL GROUP, ACTIVE AND PLACEBO-CONTROLLED, MULTICENTER STUDY TO ASSESS THE EFFICACY AND SAFETY PROFILE OF PF-06650833 IN SUBJECTS WITH ACTIVE RHEUMATOID ARTHRITIS WITH AN INADEQUATE RESPONSE TO METHOTREXATE

Brief summary

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

This is a Phase 2, multicenter, randomized, double blind, double dummy, placebo and active-controlled, parallel group study to assess the efficacy and safety of PF 06650833 at Week 12 in subjects with moderate-severe, active, RA who have had an inadequate response to MTX. PF-06650833 or matching placebo tablets will be administered orally QD under fasting conditions, and tofacitinib or matching tofacitinib placebo tablets will be administered orally BID for 12 weeks in a blinded fashion.

Study identification

NCT ID
NCT02996500
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
269 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
Nov 10, 2016 (Actual)
Primary completion
Aug 15, 2018 (Actual)
Completion
Aug 15, 2018 (Actual)
Last update posted
Feb 27, 2020

2016 – 2018

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Clinical and Translational Research Center of Alabama, PC Tuscaloosa Alabama 35406 —
Dory Hardy, PharmD Tucson Arizona 85723 —
Southern Arizona VA Health care System Tucson Arizona 85723 —
Robert W. Levin, MD,PA Clearwater Florida 33765 —
Millennium Research Ormond Beach Florida 32174 —
Arthritis & Rheumatic Care Center South Miami Florida 33143 —
Qps-Mra, Llc South Miami Florida 33143 —
Medical Associates of North Georgia Canton Georgia 30115 —
Graves Gilbert Clinic Bowling Green Kentucky 42101 —
Arthritis and Diabetes Clinic, Inc. Monroe Louisiana 71203 —
Ramesh C Gupta, M.D. Memphis Tennessee 38119 —
Accurate Clinical Management, LLC Baytown Texas 77521 —
Accurate Clinical Management, LLC Houston Texas 77004 —
Accurate Clinical Management, LLC Houston Texas 77084 —
DM Clinical Research Tomball Texas 77375 —

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 88 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02996500, 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 27, 2020 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02996500 live on ClinicalTrials.gov.

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