Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A One-Year Study To Evaluate The Effects And Safety Of CP-690,550 In Patients With Moderate To Severe Chronic Plaque Psoriasis
NCT01276639 · View on ClinicalTrials.gov ↗
Study Summary
The main objective of this study is to compare the effects of CP-690,550 with the effects of placebo in patients being treated for moderate to severe chronic plaque psoriasis. This one-year study will also evaluate the safety and tolerability of CP-690,550 versus placebo.
Conditions Studied
Interventions
- DRUG CP-690,550
- DRUG Placebo/CP-690,550
Study Locations (20)
California
- University of California, Irvine - Dermatology Research — Irvine
- Skin Surgery Medical Group, Inc. — San Diego
- Clinical Science Institute — Santa Monica
Georgia
- Atlanta Dermatology, Vein & Research Center, P.C. — Alpharetta
- Peachtree Dermatology Associates Research Center — Atlanta
- MedaPhase Inc. — Newnan
Florida
- Renstar Medical Research — Ocala
- Academic Alliance in Dermatology — Tampa
Massachusetts
- Tufts Medical Center — Boston
- Massachusetts General Hospital - Clinical Unit for Research Trials and Outcomes in Skin — Boston
New York
- New York University School of Medicine — New York
- Skin Search of Rochester, Inc. — Rochester
North Carolina
- Raleigh Radiology Blue Ridge — Raleigh
- Wake Research Associates — Raleigh
Alabama
- Radiant Research, Inc. — Birmingham
Colorado
- Cherry Creek Research, Inc. — Denver
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 901 participants |
| Start Date | 2011-03 |
| Est. Completion | 2013-04 |
| Phase | Phase 3 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01276639
The ClinicalTrials.gov registry entry for NCT01276639 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 901 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 Psoriasis appearing as the primary indexed condition, and to 2 interventions — of which CP-690,550 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: NCT01276639 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, Georgia, Florida. 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 NCT01276639 about?
NCT01276639 is a clinical study titled "A One-Year Study To Evaluate The Effects And Safety Of CP-690,550 In Patients With Moderate To Severe Chronic Plaque Psoriasis". The main objective of this study is to compare the effects of CP-690,550 with the effects of placebo in patients being treated for moderate to severe chronic plaque psoriasis. This one-year study will also evaluate the safety and tolerability of CP-690,550 versus placebo.
What is the current status of trial NCT01276639?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 901 participants. The study started on 2011-03. Estimated completion is 2013-04.
What conditions does trial NCT01276639 study?
This clinical trial studies the following conditions: Psoriasis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01276639?
The interventions under investigation include: CP-690,550 (DRUG), Placebo/CP-690,550 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01276639?
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 NCT01276639 being conducted?
This trial has 20 study locations across Alabama, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.