Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Study Comparing 2 Doses Of CP-690,550 Vs. Placebo For The Treatment Of Rheumatoid Arthritis In Patients On Other Background Arthritis Medications
NCT00856544 · View on ClinicalTrials.gov ↗
Study Summary
This Phase 3 study is intended to provide evidence that CP-690,550 dosed 5 mg BID and 10 mg BID is safe and effective when used in combination with a variety of traditional disease modifying antirheumatic drugs in adult patients with rheumatoid arthritis. It is intended to confirm the benefits of CP-690,550 in improving signs and symptoms and physical function that were observed in the Phase 2 rheumatoid arthritis studies.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG CP-690,550
Study Locations (20)
Florida
- Pfizer Investigational Site — New Port Richey
- Pfizer Investigational Site — Ocala
- Pfizer Investigational Site — Plantation
- Pfizer Investigational Site — Port Richey
- Pfizer Investigational Site — Tamarac
- Pfizer Investigational Site — Tampa
Connecticut
- Pfizer Investigational Site — Danbury
- Pfizer Investigational Site — Hamden
- Pfizer Investigational Site — Trumbull
Illinois
- Pfizer Investigational Site — Maywood
- Pfizer Investigational Site — Oakbrook Terrace
- Pfizer Investigational Site — Rockford
California
- Pfizer Investigational Site — Palo Alto
- Pfizer Investigational Site — Stanford
Colorado
- Pfizer Investigational Site — Boulder
- Pfizer Investigational Site — Denver
Georgia
- Pfizer Investigational Site — Decatur
- Pfizer Investigational Site — Marietta
Alabama
- Pfizer Investigational Site — Huntsville
Arkansas
- Pfizer Investigational Site — Jonesboro
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 795 participants |
| Start Date | 2009-05 |
| Est. Completion | 2011-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00856544
The ClinicalTrials.gov registry entry for NCT00856544 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 795 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Arthritis, Rheumatoid appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00856544 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, Connecticut, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00856544 about?
NCT00856544 is a clinical study titled "A Study Comparing 2 Doses Of CP-690,550 Vs. Placebo For The Treatment Of Rheumatoid Arthritis In Patients On Other Background Arthritis Medications". This Phase 3 study is intended to provide evidence that CP-690,550 dosed 5 mg BID and 10 mg BID is safe and effective when used in combination with a variety of traditional disease modifying antirheumatic drugs in adult patients with rheumatoid arthritis. It is intended to confirm the benefits of CP...
What is the current status of trial NCT00856544?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 795 participants. The study started on 2009-05. Estimated completion is 2011-01.
What conditions does trial NCT00856544 study?
This clinical trial studies the following conditions: Arthritis, Rheumatoid. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00856544?
The interventions under investigation include: Placebo (DRUG), CP-690,550 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00856544?
This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00856544 being conducted?
This trial has 20 study locations across Alabama, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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