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NCT00856544 · ClinicalTrials.gov registry record · Phase 3

A Study Comparing 2 Doses Of CP-690,550 Vs. Placebo For The Treatment Of Rheumatoid Arthritis In Patients On Other Background Arthritis Medications

A Phase 3 study of Arthritis, Rheumatoid, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
795
Enrollment target
20
Study locations

NCT00856544: Completed Phase 3 study of Arthritis, Rheumatoid, sponsored by Pfizer.

NCT00856544 is a Phase 3 study of Arthritis, Rheumatoid that has completed, run by Pfizer. The registered enrollment target is 795 participants, above the 612-participant average among 27 other Arthritis, Rheumatoid trials with a reported enrollment target (30% higher). The trial reports 20 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00856544, a Phase 3 study of Arthritis, Rheumatoid, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
795 participants
Enrollment target
20
Study locations

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.

Primary Outcome

ACR20 response: greater than or equal to (\>=) 20 percent (%) improvement in tender joint count (TJC); \>= 20% improvement in swollen joint count (SJC); and \>= 20% improvement in at least 3 of 5 remaining ACR core measures: participant assessment of pain; participant global assessment of disease activity; physician global assessment of disease activity; self-assessed disability (disability index of the Health Assessment Questionnaire \[HAQ\]); and C-Reactive Protein (CRP). For comparison of CP-

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

FieldValue
Enrollment Target 795 participants
Start Date 2009-05
Est. Completion 2011-01
Phase Phase 3
Pfizer

1,845 total trials

What the finished NCT00856544 record still lists

NCT00856544 is an interventional study that assigns participants to a tested intervention. The registered 795 participants enrollment target is mid-sized for trials with a published cap, above the 612-participant average among 27 other Arthritis, Rheumatoid trials with a reported enrollment target (30% higher).

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.

NCT00856544 names 20 study sites across 8 states, led by Florida, Connecticut, Illinois.

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.

What interventions are being tested in trial NCT00856544?

The interventions under investigation include: Placebo (DRUG), CP-690,550 (DRUG).

Who is sponsoring clinical trial NCT00856544?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

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.

Similar trials for Arthritis, Rheumatoid

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00856544's enrollment target sits among peer trials

795 6th of 27 higher than 22 of 27 other Arthritis, Rheumatoid trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Arthritis, Rheumatoid trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00856544, the US trial registry maintained by the National Library of Medicine. NCT00856544 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.