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NCT01309737 · ClinicalTrials.gov registry record · Phase 3

A One-Year Study To Evaluate The Efficacy And Safety Of CP-690,550 For Patients With Moderate To Severe Chronic Plaque Psoriasis

A Phase 3 study, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
960
Enrollment target

NCT01309737: Completed Phase 3 study, sponsored by Pfizer.

NCT01309737 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 960 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (24% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01309737, a Phase 3 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
960 participants
Enrollment target

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.

Primary Outcome

The PGA of psoriasis is scored on a 5-point scale, reflecting a global consideration of the erythema, induration, and scaling across all psoriatic lesions. Average erythema, induration, and scaling are scored separately over the whole body according to a 5-point severity scale (0 \[no symptom\] to 4 \[severe symptom\]). The total score was calculated as average of the 3 severity scores and rounded to the nearest whole number score to determine the PGA score and category (0=clear; 1=almost clear;

Interventions

  • DRUG CP-690,550
  • DRUG Placebo/CP-690,550

Trial Details

FieldValue
Enrollment Target 960 participants
Start Date 2011-03
Est. Completion 2013-04
Phase Phase 3
Pfizer

1,845 total trials

What the finished NCT01309737 record still lists

NCT01309737 is an interventional study that assigns participants to a tested intervention. The registered 960 participants enrollment target is mid-sized for trials with a published cap, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (24% higher).

The record links to 0 conditions, and to 2 interventions - of which CP-690,550 is the first listed.

NCT01309737 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01309737 about?

NCT01309737 is a clinical study titled "A One-Year Study To Evaluate The Efficacy And Safety Of CP-690,550 For 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 NCT01309737?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 960 participants. The study started on 2011-03. Estimated completion is 2013-04.

What interventions are being tested in trial NCT01309737?

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

Who is sponsoring clinical trial NCT01309737?

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

How this trial's enrollment target compares

Where NCT01309737's enrollment target sits among peer trials

960 330th of 2000 higher than 1,669 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT01309737, the US trial registry maintained by the National Library of Medicine. NCT01309737 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.